Source: ClinicalTrials.gov — U.S. National Library of Medicine — A database of privately and publicly funded clinical studies conducted around the world (U.S. National Library of Medicine, public domain).
This page lists clinical trials related to Peripheral Nerve Disorders from the ClinicalTrials.gov database.
Trial Summary
- Total studies: 50
- Recruiting: 20
- Active, not recruiting: 8
- Completed: 13
- Other: 9
Results are refreshed periodically and may not reflect the most current information available from ClinicalTrials.gov.
Recruiting Trials
NCT00004568 — Study of Inherited Neurological Disorders
| Status | Recruiting |
| Phase | N/A |
| Sponsor | National Institute of Neurological Disorders and Stroke (NINDS) |
| Enrollment | 3500 |
| Study Type | OBSERVATIONAL |
| Conditions | Motor Neuron Disease; Muscular Disease; Muscular Dystrophy; Peripheral Nervous System Disease |
This study is designed to learn more about the natural history of inherited neurological disorders and the role of heredity in their development. It will examine the genetics, symptoms, disease progression, treatment, and psychological and behavioral impact of diseases in the following categories: hereditary peripheral neuropathies; hereditary myopathies; muscular dystrophies; hereditary motor …
NCT00598351 — Natural History Study of Patients With Neurofibromatosis Type 2
| Status | Recruiting |
| Phase | N/A |
| Sponsor | National Institute of Neurological Disorders and Stroke (NINDS) |
| Enrollment | 269 |
| Study Type | OBSERVATIONAL |
| Conditions | Neurofibromatosis |
Objective
With this prospective natural experiment trial on neurofibromatosis type 2 (NF2) study, we hope to understand the factors leading to tumor progression and neurological disease burden in NF2.
Study Population
A total of 269 participants, ages 8-75, with a clinical or genetic diagnosis of NF2 will participate in this study.
Design
Study participants will be evaluated with a thoroug…
NCT01005654 — Prospective Comprehensive Molecular Analysis of Endocrine Neoplasms
| Status | Recruiting |
| Phase | N/A |
| Sponsor | National Cancer Institute (NCI) |
| Enrollment | 2415 |
| Study Type | OBSERVATIONAL |
| Conditions | Endocrine Tumors; Thyroid Neoplasms; Parathyroid Neoplasms; Adrenal Neoplasm; Neuroblastoma |
Background:
- Endocrine neoplasms (tumors) are among the fastest growing tumors in incidence in the United States. Furthermore, it is often difficult to distinguish between benign or malignant tumors in cancers of the thyroid, parathyroid, adrenal gland, and pancreas. More research is needed to improve detection and treatment options for patients who develop these kinds of cancer.
- Researcher…
NCT01109394 — Comprehensive Omics Analysis of Pediatric and Adult Solid Tumors and Establishment of a Repository for Related Biological Studies
| Status | Recruiting |
| Phase | N/A |
| Sponsor | National Cancer Institute (NCI) |
| Enrollment | 6035 |
| Study Type | OBSERVATIONAL |
| Conditions | Sarcoma; Endocrine Tumors; Neuroblastoma; Retinoblastoma; Renal Cancer |
Background:
- Laboratory investigators who are studying common childhood cancers are interested in developing a tissue repository to collect and store blood, serum, tissue, urine, or tumors of children who have cancer or adults who have common childhood cancers. To develop this repository, additional samples will be collected from children and adults who have been diagnosed with common childh…
NCT02390752 — Phase I Trial of TURALIO(R) (Pexidartinib, PLX3397) in Children and Young Adults With Refractory Leukemias and Refractory Solid Tumors Including Neurofibromatosis Type 1 (NF1) Associated Plexiform Neurofibromas (PN) and Tenosynovial Giant Cell Tumor …
| Status | Recruiting |
| Phase | Phase 1 |
| Sponsor | National Cancer Institute (NCI) |
| Enrollment | 54 |
| Study Type | INTERVENTIONAL |
| Conditions | Neurofibroma, Plexiform; Precursor Cell Lymphoblastic Leukemia-Lymphoma; Leukemia, Promyelocytic, Acute; Sarcoma |
| Interventions |
Background:
- Some people with cancer have solid tumors. Others have refractory leukemia. This may not go away after treatment. Researchers want to see if a drug called TURALIO(R) can shrink tumors or stop them from growing.
Objectives:
- To find the highest safe dose and side effects of TURALIO(R). To see if it helps treat certain types of cancer.
Eligibility:
- People ages 3-35 with a…
NCT02544022 — Development and Validation of Patient Reported Outcome (PRO) Measures for Individuals With Neurofibromatosis 1 (NF1) and Plexiform Neurofibromas (pNFs)
| Status | Recruiting |
| Phase | N/A |
| Sponsor | National Cancer Institute (NCI) |
| Enrollment | 476 |
| Study Type | OBSERVATIONAL |
| Conditions | Neurofibromatosis 1; Plexiform Neurofibromas |
Background:
People with neurofibromatosis 1 (NF1) who have plexiform neurofibromas (pNFs) can have pain that affects their daily lives. This study aims to improve questionnaires that measure their pain, daily living, and physical functioning.
Objectives:
To examine and improve questionnaires about daily living for people with NF1 and pNFs.
Eligibility:
People ages 5 and older with NF1 and …
NCT06490159 — Predicting Peripheral Neuropathy of Paclitaxel for Gastric Cancer
| Status | Recruiting |
| Phase | N/A |
| Sponsor | City of Hope Medical Center |
| Enrollment | 150 |
| Study Type | OBSERVATIONAL |
| Conditions | Gastric Cancer; Chemotherapy-induced Peripheral Neuropathy; Paclitaxel; Ramucirumab |
| Interventions |
Although advances in chemotherapy have improved the prognosis of gastric cancer patients, many patients still suffer from adverse events. Therefore, it is necessary to establish personalized treatment by identifying patients at high risk for side effects. Although paclitaxel-based therapy is the standard second-line treatment, peripheral neuropathy is a troublesome adverse event. The purpose of…
NCT04222413 — Metarrestin (ML-246) in Subjects With Metastatic Solid Tumors
| Status | Recruiting |
| Phase | Phase 1 |
| Sponsor | National Cancer Institute (NCI) |
| Enrollment | 116 |
| Study Type | INTERVENTIONAL |
| Conditions | Advanced Solid Tumors; Metastatic Pancreatic Cancer; Pediatric Solid Tumor; Advanced Breast Cancer; Malignant Peripheral Nerve Sheath Tumor |
| Interventions |
Background:
Metastasis is the spread of cancer from one organ to a nonadjacent organ. It causes 90% of cancer deaths. No treatment specifically prevents or reduces metastasis. Researchers hope a new drug can help. It stops cancer cells from growing and spreading further and possibly shrink cancer lesions in distant organs.
Objective:
To find a safe dose of metarrestin and to see if this dose…
NCT04755205 — A Natural History Study of Children and Adults With Olfactory Neuroblastoma
| Status | Recruiting |
| Phase | N/A |
| Sponsor | National Cancer Institute (NCI) |
| Enrollment | 525 |
| Study Type | OBSERVATIONAL |
| Conditions | Olfactory Neuroblastoma; Esthesioneuroblastoma |
Background:
Olfactory neuroblastoma (ONB) is a rare cancer. It grows from tissue in the upper part of the nose cavity, related to the sense of smell and can affect a person s sense of smell. Researchers want to better understand the health problems of people with ONB. This may help them design better treatment and supportive care studies.
Objective:
To better understand ONB-the course of the…
NCT05327114 — Efficacy and Safety Study of Nipocalimab for Adults With Chronic Inflammatory Demyelinating Polyneuropathy (CIDP)
| Status | Recruiting |
| Phase | Phase 2 / Phase 3 |
| Sponsor | Janssen Research & Development, LLC |
| Enrollment | 201 |
| Study Type | INTERVENTIONAL |
| Conditions | Polyradiculoneuropathy, Chronic Inflammatory Demyelinating |
| Interventions | ; |
The main purpose of this study is to evaluate the safety and efficacy of nipocalimab compared to placebo in delaying relapse in adults with chronic inflammatory demyelinating polyneuropathy (CIDP) who initially respond to nipocalimab in Stage A.
NCT05768139 — First-in-Human Study of Tersolisib (STX-478) as Monotherapy and in Combination With Other Antineoplastic Agents in Participants With Advanced Solid Tumors
| Status | Recruiting |
| Phase | Phase 1 / Phase 2 |
| Sponsor | Eli Lilly and Company |
| Enrollment | 880 |
| Study Type | INTERVENTIONAL |
| Conditions | Breast Cancer; Solid Tumors, Adult |
| Interventions | ; ; |
Study STX-478-101 (LY4064809) is a multipart, open-label, phase 1/2 study evaluating the safety, tolerability, pharmacokinetics (PK), and preliminary antitumor activity of STX-478 (LY4064809) in participants with advanced solid tumors with P13Ka mutations.
Part 1 will evaluate STX-478 as monotherapy in participants with advanced solid tumors. Part 2 will evaluate STX-478 therapy as combination…
NCT07690449 — Three CT Signs of Nerve-root Suffering in Low-back Sciatica: a Study of Their Frequency in Patients Referred for CT-guided Nerve-root Infiltration.
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Centre Hospitalier Universitaire de Nice |
| Enrollment | 400 |
| Study Type | OBSERVATIONAL |
| Conditions | Sciatica; Lumbosacral Radiculopathy; Low Back Pain |
| Interventions |
Retrospective, observational, single-centre study conducted at Nice University Hospital (Pasteur 2), Department of Diagnostic and Interventional Radiology. Objective: to assess the prevalence of three CT signs sought next to the clinically suspected nerve root in patients with low-back sciatica referred for CT-guided foraminal/peri-radicular infiltration: (1) nerve-root size asymmetry/hypertrop…
NCT06239272 — NRSTS2021, A Risk Adapted Study Evaluating Maintenance Pazopanib, Limited Margin, Dose-Escalated Radiation Therapy and Selinexor in Non-Rhabdomyosarcoma Soft Tissue Sarcoma (NRSTS)
| Status | Recruiting |
| Phase | Phase 1 / Phase 2 |
| Sponsor | St. Jude Children’s Research Hospital |
| Enrollment | 139 |
| Study Type | INTERVENTIONAL |
| Conditions | Adipocytic Neoplasm; Liposarcoma; Atypical Fibroxanthoma; Angiomatoid Fibrous Histiocytoma; Myoepithelioma |
| Interventions | ; ; |
The study participant has been diagnosed with non-rhabdomyosarcoma (NRSTS).
Primary Objectives
Intermediate-Risk
- To estimate the 3-year event-free survival for intermediate-risk patients treated with ifosfamide, doxorubicin, pazopanib, surgery, and maintenance pazopanib, with or without RT.
- To characterize the pharmacokinetics of pazopanib and doxorubicin in combination with ifosfamide i…
NCT07689214 — Normast3 for Adults With Diabetic Polyneuropathy
| Status | Recruiting |
| Phase | N/A |
| Sponsor | University of Roma La Sapienza |
| Enrollment | 40 |
| Study Type | INTERVENTIONAL |
| Conditions | Diabete Type 2 |
| Interventions | ; |
The goal of this clinical trial is to find out if a new supplement called Normast® 3 can help reduce nerve pain and improve nerve function in adults with diabetic polyneuropathy (DPN). DPN is a common complication of diabetes that damages nerves, often causing burning, tingling, or stabbing pain, as well as problems with the autonomic nervous system, which controls things like sweating and hear…
NCT07688915 — High-Intensity Laser Therapy Versus Transforaminal Epidural Steroid Injection in Chronic Lumbar Disc Herniation-Related Low Back and Radicular Pain
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Ankara City Hospital Bilkent |
| Enrollment | 24 |
| Study Type | INTERVENTIONAL |
| Conditions | Lumbar Disc Herniation; Chronic Low Back Pain; Radicular Pain; Lumbar Radiculopathy |
| Interventions | ; |
This prospective, randomized, single-blinded, controlled clinical trial aims to compare the effectiveness of high-intensity laser therapy and fluoroscopy-guided transforaminal epidural steroid injection in patients with chronic low back pain and lumbar radiculopathy. Eligible patients will be randomized into two parallel groups. One group will receive high-intensity laser therapy, and the other…
NCT07689331 — Hungarian National Systemic Amyloidosis Registry
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Semmelweis University |
| Enrollment | 300 |
| Study Type | OBSERVATIONAL |
| Conditions | Systemic Amyloidosis; ATTR Amyloidosis; AL Amyloidosis; Amyloid Cardiomyopathy |
This registry is an observational, multicenter, retrospective and prospective, non-pharmacological study designed to collect and analyze data from patients with systemic amyloidosis treated in inpatient and outpatient cardiology, hematology, nephrology, and neurology departments across Hungary. The registry was established in 2025.
NCT07540221 — A Study to Evaluate the Pharmacokinetics and Safety of XEMBIFY Versus Gamunex-C in Participants With Chronic Inflammatory Demyelinating Polyradiculoneuropathy
| Status | Recruiting |
| Phase | Phase 3 |
| Sponsor | Grifols Therapeutics LLC |
| Enrollment | 40 |
| Study Type | INTERVENTIONAL |
| Conditions | CIDP (Chronic Inflammatory Demyelinating Polyradiculoneuropathy) |
| Interventions | ; |
The main goal of the study is to find out whether XEMBIFY, given once a week under the skin, provides similar levels of immunoglobulin G in the blood over time as Gamunex-C, which is given into a vein once every 3 weeks in people with CIDP.
Participants with CIDP will first have up to 28 days of screening to make sure they can join the study. Those who qualify will then start a 19-week treatme…
NCT07558733 — Sapanisertib and Serabelisib (PIKTOR) in Various Combinations in Patients With HR+/HER2- Advanced/Metastatic Breast Cancer
| Status | Recruiting |
| Phase | Phase 1 / Phase 2 |
| Sponsor | Faeth Therapeutics |
| Enrollment | 32 |
| Study Type | INTERVENTIONAL |
| Conditions | HR+ HER2- Breast Cancer |
| Interventions | ; ; |
The study is a Phase 1b/2, multi-center, open-label, dose escalation trial evaluating the safety and preliminary efficacy of sapanisertib and serabelisib (PIKTOR) with fulvestrant and/or other anticancer therapies in participants with HR+/HER2- advanced/metastatic breast cancer.
NCT07660913 — Effectiveness of Matrix Rhythm Therapy on Carpal Tunnel Syndrome
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Izmir Bakircay University |
| Enrollment | 84 |
| Study Type | INTERVENTIONAL |
| Conditions | Carpal Tunnel Syndrome |
| Interventions | ; ; |
The purpose of this study is to investigate the effects of matrix rhythm therapy, applied in addition to conventional treatment, on symptom severity, function, grip and pinch strength, and quality of life in patients with carpal tunnel syndrome.
NCT07661290 — Effect of High-Power Laser Therapy on Disc Morphology and Functional Outcome in Patients With Cervical Radiculopathy
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Cairo University |
| Enrollment | 60 |
| Study Type | INTERVENTIONAL |
| Conditions | Radiculopathy |
| Interventions | ; |
The study aims to evaluate the effectiveness of high-power laser therapy (HPLT) in patients with cervical radiculopathy, focusing on its impact on disc morphology, and overall functional activity
Active, Not Recruiting
NCT00924196 — Natural History Study of Patients With Neurofibromatosis Type I
| Status | Active, not recruiting |
| Phase | N/A |
| Sponsor | National Cancer Institute (NCI) |
| Enrollment | 259 |
| Study Type | OBSERVATIONAL |
| Conditions | Neurofibromatosis Type 1; Malignant Peripheral Nerve Sheath Tumor; Plexiform Neurofibroma; Optic Glioma; Neurofibroma |
Background:
Neurofibromatosis Type 1 (NF1) is a genetic disorder in which patients are at increased risk of developing tumors (usually non-cancerous) of the central and peripheral nervous system. The disease affects essentially every organ system.
The natural course of NFI over time is poorly understood. For most patients the only treatment option is surgery. A better understanding of NF1 may…
NCT03635632 — C7R-GD2.CART Cells for Patients With Relapsed or Refractory Neuroblastoma and Other GD2 Positive Cancers (GAIL-N)
| Status | Active, not recruiting |
| Phase | Phase 1 |
| Sponsor | Baylor College of Medicine |
| Enrollment | 94 |
| Study Type | INTERVENTIONAL |
| Conditions | Relapsed Neuroblastoma; Refractory Neuroblastoma; Relapsed Osteosarcoma; Relapsed Ewing Sarcoma; Relapsed Rhabdomyosarcoma |
| Interventions |
This study is for patients with neuroblastoma, sarcoma, uveal melanoma, breast cancer, or another cancer that expresses a substance on the cancer cells called GD2. The cancer has either come back after treatment or did not respond to treatment. Because there is no standard treatment at this time, patients are asked to volunteer in a gene transfer research study using special immune cells called…
NCT04001829 — Taxane and Taxane-Induced Peripheral Neuropathy in African American Patients With Stage I-III Breast Cancer
| Status | Active, not recruiting |
| Phase | Phase 2 |
| Sponsor | ECOG-ACRIN Cancer Research Group |
| Enrollment | 249 |
| Study Type | INTERVENTIONAL |
| Conditions | Anatomic Stage I Breast Cancer AJCC v8; Anatomic Stage IA Breast Cancer AJCC v8; Anatomic Stage IB Breast Cancer AJCC v8; Anatomic Stage II Breast Cancer AJCC v8; Anatomic Stage IIA Breast Cancer AJCC v8 |
| Interventions | ; ; |
This phase II trial studies whether a prior germline predictor of taxane-induced peripheral neuropathy (TIPN) can help identify a subgroup of patients who are at higher risk of chemotherapy-induced peripheral neuropathy in African American patients with stages I-III breast cancer. The study also investigates whether docetaxel maybe work better than paclitaxel with regard to TIPN rate/severity a…
NCT03975829 — Pediatric Long-Term Follow-up and Rollover Study
| Status | Active, not recruiting |
| Phase | Phase 4 |
| Sponsor | Novartis Pharmaceuticals |
| Enrollment | 163 |
| Study Type | INTERVENTIONAL |
| Conditions | Diffuse Astrocytoma; Anaplastic Astrocytoma; Astrocytoma; Oligodendroglioma, Childhood; Anaplastic Oligodendroglioma |
| Interventions | ; |
A roll-over study to assess long-term effect in pediatric patients treated with dabrafenib and/or trametinib.
NCT05357469 — Innovative Treatment of Chemotherapy-Induced Painful Peripheral Neuropathy in Adolescents and Young Adults With Cancer: A Two Arm Pilot Study
| Status | Active, not recruiting |
| Phase | N/A |
| Sponsor | M.D. Anderson Cancer Center |
| Enrollment | 30 |
| Study Type | INTERVENTIONAL |
| Conditions | Peripheral Neuropathy |
| Interventions | ; |
To evaluate the efficacy and safety of Scrambler therapy (ST) for chemotherapy-induced painful peripheral neuropathy (CIPN), and the impact of ST on physical functioning and quality of life (QoL) in adolescents and young adults (AYA) cancer patients.
In this proposed study, we will conduct a two-arm prospective, randomized wait-list controlled clinical trial to investigate the effectiveness of…
NCT05619302 — Molecular Imaging of Myocardial Fibrosis in Cardiac Amyloidosis
| Status | Active, not recruiting |
| Phase | Phase 3 |
| Sponsor | Brigham and Women’s Hospital |
| Enrollment | 18 |
| Study Type | INTERVENTIONAL |
| Conditions | Cardiac Amyloidosis |
| Interventions |
The primary aim of our pilot study is to determine whether fibrosis in the heart can be measured with [68Ga]CBP8, a positron emission tomography (PET) probe, using PET/magnetic resonance imaging (MRI) imaging, in 30 individuals with documented cardiac amyloidosis. The investigators will also enroll 15 individuals with recent myocardial infarction and 15 individuals with hypertrophic cardiomyo…
NCT06151600 — A Prospective Natural History and Outcome Measure Discovery Study of Charcot-Marie-Tooth Disease, Type 4J
| Status | Active, not recruiting |
| Phase | N/A |
| Sponsor | Elpida Therapeutics SPC |
| Enrollment | 20 |
| Study Type | OBSERVATIONAL |
| Conditions | Peripheral Neuropathy; Neuro-Degenerative Disease; Neuromuscular Diseases |
This is a multicenter, longitudinal, prospective observational natural history study of subjects with a molecularly confirmed diagnosis of CMT4J. The study will enroll 20 subjects of any age into a uniform protocol for follow-up and evaluations. Subject visits will occur every 12 months + 4 weeks for up to 2 years.
NCT06646731 — Cryoneurolysis for Painful Diabetic Neuropathy of the Foot
| Status | Active, not recruiting |
| Phase | N/A |
| Sponsor | University of California, San Diego |
| Enrollment | 30 |
| Study Type | INTERVENTIONAL |
| Conditions | Painful Diabetic Peripheral Neuropathy (PDPN) |
| Interventions | ; |
The study is a single-center, randomized, participant- and observer-masked, human-subjects, post-market clinical pilot study to investigate the use of ultrasound-guided percutaneous cryoneurolysis to treat diabetic neuropathy of the foot. A prolonged nerve block may be provided by freezing the nerve using a technique called “cryoneurolysis”. With cryoneurolysis and ultrasound machines, a small …
Not Yet Recruiting
NCT07691359 — Osteoporotic Fracture and Lidocaine Plaster 5% for Neuropathic Pain preventioN
| Status | Not yet recruiting |
| Phase | Phase 4 |
| Sponsor | University Hospital, Clermont-Ferrand |
| Enrollment | 30 |
| Study Type | INTERVENTIONAL |
| Conditions | Osteoporotic Vertebral Fracture; Neuropathic Pain |
| Interventions |
Osteoporotic vertebral fractures may lead to chronic pain with a neuropathic component, which is often underdiagnosed and undertreated in older adults. This proof-of-concept randomized controlled trial aims to evaluate whether early application of a 5% lidocaine plaster can prevent the development of neuropathic pain following an osteoporotic vertebral fracture. Participants will be randomized …
NCT07240649 — Emerging Indications for Hyperbaric Oxygen Treatment
| Status | Not yet recruiting |
| Phase | Phase 4 |
| Sponsor | Jay C. Buckey Jr. |
| Enrollment | 100 |
| Study Type | INTERVENTIONAL |
| Conditions | Post-COVID-19 Condition; Ulcerative Colitis; Crohn Disease; Calciphylaxis; Frostbite |
| Interventions | ; |
This study will evaluate the effectiveness of hyperbaric oxygen therapy (HBOT) on treating emerging indications (i.e., conditions that have shown to potentially benefit from HBOT) using the Multicenter Registry for Hyperbaric Oxygen Treatment. The study team aims to collect ongoing data on how well HBOT treats these emerging indications, and to add these data to the growing HBO Registry. The re…
NCT07687082 — Prevalence and Risk Factors for Chronic Post-Surgical Pain Following Video-Assisted Thoracic Surgery : The EVATHO Prospective Bicentric Cohort Study.
| Status | Not yet recruiting |
| Phase | N/A |
| Sponsor | University Hospital, Montpellier |
| Enrollment | 400 |
| Study Type | OBSERVATIONAL |
| Conditions | Chronic Post-surgical Pain; Postoperative Pain After Thoracic Surgery; Neuropathic Pain; Thoracic Surgical Procedures |
Chronic post-surgical pain (CPSP) remains a common complication after thoracic surgery and may significantly impair patients’ quality of life. Although the widespread adoption of video-assisted thoracic surgery (VATS) has reduced surgical trauma and improved postoperative recovery, a substantial proportion of patients still develop persistent pain.
The EVATHO study is a multicenter prospective…
NCT07683598 — DLBS1033 as Adjunctive Therapy for Patients With Diabetic Neuropathy
| Status | Not yet recruiting |
| Phase | N/A |
| Sponsor | RS H Adam Malik |
| Enrollment | 80 |
| Study Type | INTERVENTIONAL |
| Conditions | Diabetic Neuropathy |
| Interventions | ; |
This study will evaluate the effect of DLBS1033 as adjunctive therapy in patients with diabetic neuropathy. Diabetic neuropathy is a common complication of diabetes that can cause numbness, tingling, pain, impaired nerve function, and reduced quality of life.
Participants with diabetic neuropathy will be randomly assigned to receive either DLBS1033 plus standard therapy or placebo plus standar…
NCT07681921 — Randomized Clinical Investigation of Photobiomodulation (PBM) for the Management of Early Peripheral Neuropathy Related to Medical Oncologic Therapy
| Status | Not yet recruiting |
| Phase | N/A |
| Sponsor | Jules Bordet Institute |
| Enrollment | 98 |
| Study Type | INTERVENTIONAL |
| Conditions | Chemotherapy Induced Peripheral Neuropathy |
| Interventions |
Chemotherapy-induced peripheral neuropathy (CIPN) is one of the common complications of cancer treatment and involves paresthesia, numbness and/or burning pain in distal limbs. This condition has a high health impact because it is associated with psychological distress, fall risk, and poor sleep quality. Furthermore, it impairs patients’ daily activities and thereby decreases their quality of l…
NCT07682324 — Daily, Encapsulated, Green Tea Extract to Mitigate Neuropathic Pain in Patients With Established Cancer-Associated Neuropathic Pain
| Status | Not yet recruiting |
| Phase | Phase 1 |
| Sponsor | University of Alabama at Birmingham |
| Enrollment | 20 |
| Study Type | INTERVENTIONAL |
| Conditions | Neuropathic Pain; Cancer Treatment |
| Interventions | ; |
The overall objective of this study is to test an intervention of green tea extract (GTE) to mitigate neuropathic pain in patients, specifically cancer survivors, receiving supportive palliative care. Our central hypothesis is that daily, oral, encapsulated GTE will mitigate neuropathic pain, as longitudinally measured by the validated Douleur Neuropathique 4 (DN4) and blood protein biomarkers …
NCT07686094 — Placental Cells for Diabetic Foot Ulcers
| Status | Not yet recruiting |
| Phase | Phase 1 |
| Sponsor | Wake Forest University Health Sciences |
| Enrollment | 12 |
| Study Type | INTERVENTIONAL |
| Conditions | Diabetic Foot Ulcer |
| Interventions |
The purpose of this research study is to test the safety of placental stem cells to treat non-healing diabetic foot ulcers.
Completed Trials
NCT00111384 — Study of Disease Severity in Adults With Neurofibromatosis Type 1 (NF1)
| Status | Completed |
| Phase | N/A |
| Sponsor | National Cancer Institute (NCI) |
| Enrollment | 313 |
| Study Type | OBSERVATIONAL |
| Conditions | Neurofibromatosis Type 1; Legius Syndrome |
This study may identify genes that predict the seriousness of neurofibromatosis type 1 (NF1). Finding these genes may explain why some people with NF1 have more medical problems than others. The study will also examine medical problems in NF1 that are rarely seen and are not well understood.
Male and female patients with NF1 who have gone through puberty may be eligible for this study, as well…
NCT00314119 — Natural History and Biology of Skin Neurofibromas in Neurofibromatosis Type 1
| Status | Completed |
| Phase | N/A |
| Sponsor | National Cancer Institute (NCI) |
| Enrollment | 17 |
| Study Type | OBSERVATIONAL |
| Conditions | Neurofibromatosis Type 1; Neurofibroma |
This study will explore the growth of dermal neurofibromas (skin tumors) in patients with neurofibromatosis type 1 (NF1). Investigators will try to learn: 1) how fast (or slow) these benign tumors grow in NF1, 2) how often new tumors appear and 3) what genes are involved in the growth of the tumors.
Men and women between 20 and 50 years of age diagnosed with NF1 and their biological parents ar…
NCT00664313 — TBTC Study 30: Safety and Tolerability of Low Dose Linezolid in MDR TB
| Status | Completed |
| Phase | Phase 1 / Phase 2 |
| Sponsor | Centers for Disease Control and Prevention |
| Enrollment | 36 |
| Study Type | INTERVENTIONAL |
| Conditions | Multi-drug Resistant Tuberculosis; Extensively Drug Resistant Tuberculosis |
| Interventions | ; |
This study evaluated the safety and tolerability of low-dose linezolid (600 mg once daily) administered for 16 weeks as part of an optimized background regimen for the treatment of multidrug-resistant tuberculosis (MDR-TB).
NCT05374876 — Hand Therapy Intervention Versus Traditional Occupational Therapy to Prevent Chemotherapy Induced Peripheral Neuropathy
| Status | Completed |
| Phase | N/A |
| Sponsor | HonorHealth Research Institute |
| Enrollment | 49 |
| Study Type | INTERVENTIONAL |
| Conditions | Adenocarcinoma of Pancreas |
| Interventions | ; |
A pilot randomized feasibility trial with a blinded evaluator.
NCT04868123 — Effects of TENS and Mindfulness Meditation in Persons With HIV-related Neuropathy
| Status | Completed |
| Phase | N/A |
| Sponsor | Rutgers University |
| Enrollment | 36 |
| Study Type | INTERVENTIONAL |
| Conditions | HIV Infections |
| Interventions | ; |
This study is to explore the effects of transcutaneous nerve stimulation (TENS) and mindfulness meditation in persons living with HIV (PLHIV) and painful neuropathy in the feet.
NCT06062108 — Prevalence of Pain in Hospitalized Cirrhotic Patients
| Status | Completed |
| Phase | N/A |
| Sponsor | Centre Hospitalier Intercommunal de Toulon La Seyne sur Mer |
| Enrollment | 30 |
| Study Type | OBSERVATIONAL |
| Conditions | Cirrhosis; Hepatic Fibrosis; Pain, Acute; Pain, Chronic; Pain, Neuropathic |
| Interventions |
According to the WHO, pain is an “unpleasant sensory and emotional experience, linked to existing or potential tissue damage, or described in terms suggestive of such damage”. It is a legal obligation to evaluate and take care of it (law of 03/04/2022). However, there are still areas where this is not addressed, particularly in cirrhotic patients (Piano V et al. 2023).
The global prevalence of…
NCT07005947 — Long COVID-19 Cutaneous Signatures: An ARPA Funded Research Project
| Status | Completed |
| Phase | N/A |
| Sponsor | CND Life Sciences |
| Enrollment | 237 |
| Study Type | OBSERVATIONAL |
| Conditions | Long COVID-19; Acute COVID-19; Postural Orthostatic Tachycardia Syndrome (POTS); Diabetic Neuropathy |
This is a prospective, longitudinal study involving 300 participants for a single visit to compare Long COVID-19 neurocutaneous biosignatures with those of other disorders affecting the sensory and autonomic nervous system.
NCT07685691 — RELATIONSHIP BETWEEN CLINICAL STATUS AND NERVE CONDUCTION TEST FINDINGS IN PATIENTS WITH UNILATERAL HEMIPLEGIA
| Status | Completed |
| Phase | N/A |
| Sponsor | Baskent University |
| Enrollment | 73 |
| Study Type | OBSERVATIONAL |
| Conditions | Stroke; Hemiplegia; Intracranial Hemorrhage, Spontaneous |
| Interventions |
Stroke-related hemiplegia may be accompanied by peripheral nerve conduction abnormalities, which may contribute to motor impairment and functional limitations. However, the frequency of these abnormalities and their relationship with clinical status have not been fully characterized. This single-center observational study aims to evaluate the frequency of peripheral nerve conduction abnormaliti…
NCT07458737 — Pelvic Floor Shear-Wave Elastography in Healthy and Pudendal Neuralgia Women
| Status | Completed |
| Phase | N/A |
| Sponsor | Comenius University |
| Enrollment | 94 |
| Study Type | OBSERVATIONAL |
| Conditions | Pudendal Nerve; Healthy Women |
| Interventions | ; ; |
This study will compare superficial pelvic floor shear-wave elastography between healthy women and women with pudendal neuralgia.
NCT07583901 — Effects of Gaze Stabilization Exercises and Optokinetic Training in Peripheral Vestibular Disorders
| Status | Completed |
| Phase | N/A |
| Sponsor | Foundation University Islamabad |
| Enrollment | 32 |
| Study Type | INTERVENTIONAL |
| Conditions | Nystagmus; Optokinetic Nystagmus |
| Interventions | ; |
This study compares the effectiveness of Gaze Stabilization Exercises and Optokinetic Training in improving dizziness, balance, and confidence in individuals with peripheral vestibular disorders.
NCT07683338 — Effects of Pregabalin Ultrasound Therapy and Nerve Exercises on Pain and Sensation in Diabetic Nerve Damage
| Status | Completed |
| Phase | N/A |
| Sponsor | Syeda Khatoon e Jannat Welfare Foundation |
| Enrollment | 24 |
| Study Type | INTERVENTIONAL |
| Conditions | Peripheral Diabetic Neuropathy; Diabetic Neuropathic Pain; Painful Diabetic Peripheral Neuropathy |
| Interventions | ; ; |
Peripheral diabetic neuropathy (PDN) is a common complication of diabetes mellitus characterized by neuropathic pain, sensory disturbances, and impaired quality of life. This study aims to determine the effects of pregabalin phonophoresis combined with sural nerve flossing on neuropathic pain and sensory function in individuals with peripheral diabetic neuropathy. Participants will be randomly …
NCT07380880 — Comparison of Proprioceptive Neuromuscular Training and Sensory Re-education in Patients With Diabetic Peripheral Neuropathy
| Status | Completed |
| Phase | N/A |
| Sponsor | Montiha Azeem |
| Enrollment | 80 |
| Study Type | INTERVENTIONAL |
| Conditions | Diabetic Peripheral Neuropathy |
| Interventions | ; |
Diabetic peripheral neuropathy (DPN) is a common complication of diabetes mellitus and is associated with sensory loss, impaired proprioception, balance deficits, and altered gait patterns, which significantly increase the risk of falls and functional dependence. Rehabilitation strategies targeting sensory and proprioceptive impairments are essential to improve postural control and mobility in …
NCT07335822 — The Effectiveness of Low-Level Laser Therapy in the Treatment of Meralgia Paresthetica
| Status | Completed |
| Phase | N/A |
| Sponsor | Istanbul Training and Research Hospital |
| Enrollment | 36 |
| Study Type | INTERVENTIONAL |
| Conditions | Meralgia Paresthetica; Lateral Femoral Cutaneous Nerve Entrapment |
| Interventions | ; |
Patients diagnosed with meralgia paresthetica via electromyography (EMG), who present with neuropathic complaints on the lateral thigh to the Physical Medicine and Rehabilitation outpatient clinics of our hospital, will be included in the study after reviewing exclusion criteria. Patients will be randomized into two equal groups using a sealed-envelope system. The treatment group will receive l…
Other (No longer available)
NCT03874455 — Tazemetostat Expanded Access Program for Adults With Solid Tumors
| Status | No longer available |
| Phase | N/A |
| Sponsor | Epizyme, Inc. |
| Enrollment | N/A |
| Study Type | EXPANDED_ACCESS |
| Conditions | Epithelioid Sarcoma (Ex-US Only); Spindle Cell Sarcoma; Sinonasal Carcinoma; Small Cell Carcinoma of the Ovary Hypercalcemic Type; Thoracic Sarcoma |
| Interventions |
Patients with a diagnosis listed under “conditions” below are eligible to be considered for the EAP. These conditions must be serious or life-threatening at the time of enrollment and appropriate, comparable, or satisfactory alternative treatments must have been tried without clinical success. Patients with conditions not listed under “conditions” below are not eligible for the tazemetostat EAP.
Other (Terminated)
NCT05891847 — Non-interventional Study of Patients With PN NF1 Starting Selumetinib in Russia
| Status | Terminated |
| Phase | N/A |
| Sponsor | AstraZeneca |
| Enrollment | 150 |
| Study Type | OBSERVATIONAL |
| Conditions | Neurofibroma |
The purpose of this study is to evaluate the effectiveness, safety of selumetinib and patient’s parameters of symptomatic inoperable PN NF1 in real clinical practice in Russia