Clinical Trials for Pain

Currently registered clinical trials for Pain from ClinicalTrials.gov. 16 recruiting, 50 total studies.

This content is for informational purposes only. Always consult a healthcare professional.

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 Pain from the ClinicalTrials.gov database.

Trial Summary

  • Total studies: 50
  • Recruiting: 16
  • Active, not recruiting: 6
  • Completed: 18
  • Other: 10

Results are refreshed periodically and may not reflect the most current information available from ClinicalTrials.gov.

Recruiting Trials

NCT00051857 — MRI Study of Musculoskeletal Function

StatusRecruiting
PhaseN/A
SponsorNational Institutes of Health Clinical Center (CC)
Enrollment750
Study TypeOBSERVATIONAL
ConditionsAbnormalities; Imaging; Patellofemoral Pain Syndrome

This study will use magnetic resonance imaging (MRI) and ultrasound images to study how muscles, tendons, and bones work together to cause motion. The procedure is one of several tools being developed to characterize normal and impaired musculoskeletal function, with the goal of developing improved methods of diagnosis and treatment of movement disorders.

Healthy normal volunteers must be age …

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.

StatusRecruiting
PhaseN/A
SponsorCentre Hospitalier Universitaire de Nice
Enrollment400
Study TypeOBSERVATIONAL
ConditionsSciatica; 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…

NCT07689214 — Normast3 for Adults With Diabetic Polyneuropathy

StatusRecruiting
PhaseN/A
SponsorUniversity of Roma La Sapienza
Enrollment40
Study TypeINTERVENTIONAL
ConditionsDiabete 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…

NCT06349772 — Zynrelef vs Exparel: The Battle of Postoperative Pain Control After Robotic Sleeve Gastrectomy

StatusRecruiting
PhaseEarly Phase 1
SponsorTexas Tech University Health Sciences Center
Enrollment130
Study TypeINTERVENTIONAL
ConditionsPost Operative Pain
Interventions;

The purpose of this study is to evaluate the use of an injectable combination of bupivacaine and meloxicam (Zynrelef) vs injectable liposomal bupivacaine (Exparel), two extended local anesthesia strategies currently approved by FDA and on the market for post-surgical pain control. The investigators plan on randomizing study participants to either Exparel or Zynrelef at the closure site of robot…

NCT07091682 — Safety and Clinical Performance of the Freesolve Resorbable Magnesium Scaffold System in the Treatment of Subjects With Long de Novo Lesions

StatusRecruiting
PhaseN/A
SponsorBiotronik AG
Enrollment100
Study TypeINTERVENTIONAL
ConditionsCoronary Artery Disease; Atherosclerosis of Coronary Artery; Myocardial Ischemia; Ischemic Heart Disease; Acute Coronary Syndromes
Interventions

The study objective is the assessment of safety and clinical performance of Freesolve 35- and 40-mm in de novo coronary artery lesions up to 38 mm length.

NCT06915909 — Robotic Prostatectomy Artificial Intelligence Low Pressure Pain (RALP) Trial

StatusRecruiting
PhaseN/A
SponsorEast and North Hertfordshire NHS Trust
Enrollment100
Study TypeINTERVENTIONAL
ConditionsProstate Cancer (Adenocarcinoma); Prostate Cancer (Post Prostatectomy); Prostate Cancer Surgery; Prostate Cancers; Prostate Neoplasm
Interventions

The ‘Robotic Prostatectomy Artificial Intelligence Low Pressure Pain Study Trial’ aims to assess the feasibility of being able to review operative outcomes such as pain when comparing two commonly used surgical devices for the removal of prostate cancers. The data collected will inform methodologies for future, larger, multi-center trials investigating pain in patients undergoing prostate cance…

NCT06351046 — Preventive Interventions for Chronic Pain Worsening

StatusRecruiting
PhaseN/A
SponsorRigshospitalet, Denmark
Enrollment44
Study TypeINTERVENTIONAL
ConditionsChronic Non-Cancer Pain
Interventions

This is an open label randomized controlled trial (RCT), which will be conducted with patients of the Copenhagen Wound Healing Center at Bispebjerg Hospital in Copenhagen (DK). The trial has two arms (1:1): A Virtual Reality based Pain Self-management (VRPS) program group, and a control group (usual care). Included will be 44 patients at least 18 years old; fluent in the Danish language; compla…

NCT07267052 — Acute Effects of Transcutaneous Electrical Nerve Stimulation at Acupoints on Nociceptive Transmission

StatusRecruiting
PhaseN/A
SponsorChina Medical University Hospital
Enrollment35
Study TypeINTERVENTIONAL
ConditionsPain Management
Interventions;

The goal of this clinical trial is to learn if transcutaneous electrical nerve stimulation (TENS) applied to acupoints can modulate pain transmission and cortical processing in healthy adult volunteers. The main questions it aims to answer are:

  • Does TENS at Zhongzhu (SJ3) and Hegu (LI4) change pain-related evoked potentials (PREPs)?
  • Does acupoint electrical stimulation alter nociceptive pa…

NCT07689461 — VR Effects After Hip Replacement Surgery Pain

StatusRecruiting
PhaseN/A
SponsorAdiyaman University
Enrollment80
Study TypeINTERVENTIONAL
ConditionsVirtual Reality; Hip Arthropathy; Comfort; Anxiety; Pain, Postoperative
Interventions

Total Hip Arthroplasty (THA), a procedure performed to enhance the quality of life, is accompanied by postoperative challenges such as pain and anxiety that adversely affect patient comfort. Inadequate management of these complications can prolong the length of hospital stay, delay recovery, lead to functional impairments, and elevate the risk of chronic pain development. Conventional pharmacol…

NCT07680998 — Performance and Safety of the ANTALGEEK® Thess Monitoring Medical Device in the Outpatient Management of Acute Pain and Postoperative Recovery

StatusRecruiting
PhaseN/A
SponsorCentre Hospitalier Universitaire de Nīmes
Enrollment150
Study TypeINTERVENTIONAL
ConditionsPost Operative Pain; Chronic Pain
Interventions

Acute postoperative pain (APOP) is a major public health problem, affecting nearly 10 million patients in France each year. Effective analgesic therapy in the first postoperative week is a key factor in reducing early postoperative morbidity and mortality. Poorly controlled APOP is a major risk factor for chronic postoperative pain. In France today, more and more patients undergo surgical proce…

NCT07443930 — Musicians’ Health Education in D-A-CH

StatusRecruiting
PhaseN/A
SponsorUniversity Medical Center Goettingen
Enrollment39
Study TypeOBSERVATIONAL
ConditionsEducation; Medicine; Dentistry; Orofacial Pain

Professional musicians are often exposed to significant physical and psychological strain. Long hours of playing, high muscle tension in the head and neck area, and performance-related stress can lead to problems such as musculoskeletal pain, jaw joint disorders, facial pain, and reduced oral health. Although these health issues are common, preventive strategies and structured health education …

NCT07605546 — RAD ONC FREEDOM Oncology Pain

StatusRecruiting
PhaseN/A
SponsorJonsson Comprehensive Cancer Center
Enrollment19
Study TypeINTERVENTIONAL
ConditionsCancer Pain
Interventions

The investigators propose to conduct a study in medically refractory cancer pain patients utilizing radiosurgery to ablate the pituitary hypophysis, as well as neuromodulate the centromedian and parafascicular complexes within the thalami - the so-called triple target. This involves treating the pituitary hypophysis and thalamus to a dose of 90 Gy. These patients will have previously failed to …

NCT07235098 — Effect of a Music Intervention in Reducing Distress and Pain in Patients With Lung Cancer Undergoing Mini-invasive Surgery

StatusRecruiting
PhaseN/A
SponsorOncology Institute of Southern Switzerland
Enrollment74
Study TypeINTERVENTIONAL
ConditionsLung Cancer (Suspected or Confirmed)
Interventions

This study aims at evaluating whether music therapy intervention is effective in decreasing psychological (distress) and physical symptoms (pain) in patients with suspected or diagnosed lung cancer undergoing minimally invasive lung surgery.

NCT07054801 — IA Lidocaine and Methylprednisolone for Headache Associated With Subarachnoid Hemorrhage

StatusRecruiting
PhasePhase 2
SponsorDaniel Raper, MBBS
Enrollment25
Study TypeINTERVENTIONAL
ConditionsHeadaches Associated With Subarachnoid Hemorrhage (SAH)
Interventions;

Subarachnoid hemorrhage (SAH) is a type of bleeding around the brain that can cause sudden and severe headaches. These headaches can be debilitating and persist for weeks, significantly impacting a patient’s comfort and recovery. Many patients require opioids for pain control, which can lead to side effects such as drowsiness, constipation, and dependency. There is a need for new treatment stra…

NCT07689396 — Predictors of Treatment Expectations in Myofascial Pain Syndrome

StatusRecruiting
PhaseN/A
SponsorKTO Karatay University
Enrollment85
Study TypeOBSERVATIONAL
ConditionsMyofascial Pain Syndromes

This cross-sectional study aims to determine the predictors of treatment expectations in individuals with myofascial pain syndrome (MPS). MPS is one of the most common causes of musculoskeletal pain and is associated with reduced quality of life. Patients’ pre-treatment expectations are known to influence clinical outcomes, yet the factors that predict these expectations have not been establish…

NCT07434895 — Repeated CBD Administration and Cannabis Outcomes

StatusRecruiting
PhaseEarly Phase 1
SponsorHannah Harris
Enrollment23
Study TypeINTERVENTIONAL
ConditionsCannabis; Abuse Liability; Experimental Pain in Healthy Human Participants
Interventions; ;

This outpatient study examines how cannabidiol (CBD) affects the behavioral and pain-relieving effects of cannabis.

Active, Not Recruiting

NCT03214510 — Thoracic Epidural Analgesia or Four-Quadrant Transversus Abdominus Plane Block in Reducing Pain in Patients Undergoing Liver Surgery

StatusActive, not recruiting
PhasePhase 3
SponsorM.D. Anderson Cancer Center
Enrollment101
Study TypeINTERVENTIONAL
ConditionsLiver and Intrahepatic Bile Duct Disorder
Interventions; ;

This phase III trial studies how well thoracic epidural analgesia or four-quadrant transversus abdominus plane block works in reducing pain in patients undergoing liver surgery. It is not yet known whether thoracic epidural analgesia or four-quadrant transversus abdominus plane block may help people to recover more completely and more quickly after surgery.

NCT04618471 — Paresthesia-Free Fast-Acting Subperception (FAST) Study

StatusActive, not recruiting
PhaseN/A
SponsorBoston Scientific Corporation
Enrollment177
Study TypeINTERVENTIONAL
ConditionsChronic Pain
Interventions

Study to evaluate the effectiveness of FAST-SCS (fast-acting paresthesia-free therapy) and additional SCS therapy options in patients with chronic pain using Boston Scientific WaveWriter SCS Systems.

NCT04754165 — Postoperative VR for Recovery After Bariatric Surgery

StatusActive, not recruiting
PhaseN/A
SponsorBeth Israel Deaconess Medical Center
Enrollment66
Study TypeINTERVENTIONAL
ConditionsBariatric Surgery Candidate; Postoperative Pain; Postoperative Complications
Interventions

The objective of this study is to investigate whether the addition of immersive virtual reality (VR) in the immediate postoperative period to an enhanced recovery after surgery (ERAS) protocol could improve postoperative recovery from bariatric surgery.

NCT05357469 — Innovative Treatment of Chemotherapy-Induced Painful Peripheral Neuropathy in Adolescents and Young Adults With Cancer: A Two Arm Pilot Study

StatusActive, not recruiting
PhaseN/A
SponsorM.D. Anderson Cancer Center
Enrollment30
Study TypeINTERVENTIONAL
ConditionsPeripheral 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…

NCT05703178 — Web-based Pain Coping Skills Training for Breast Cancer Survivors With AI-Associated Arthralgia

StatusActive, not recruiting
PhasePhase 3
SponsorNorthwestern University
Enrollment452
Study TypeINTERVENTIONAL
ConditionsBreast Cancer; Arthralgia; Pain, Chronic
Interventions;

The main goal of this clinical trial is to test benefits of completing online pain coping skills training program in women who have been diagnosed with stage I-III breast cancer, who have completed their primary cancer treatment, who are taking an AI medication, and who have arthralgia. Arthralgia is a type of joint, bone, and muscle pain that is a common side effect of AI medications. The main…

NCT06853626 — One-hoUr Troponin Using a High-sensitivity Point-Of-Care Assay in Emergency Primary Care

StatusActive, not recruiting
PhaseN/A
SponsorUniversity of Oslo
Enrollment2500
Study TypeINTERVENTIONAL
ConditionsAcute Myocardial Infarction (AMI); Chest Pain; Acute Coronary Syndromes (ACS); Non-cardiac Chest Pain; Troponin
Interventions

Acute chest pain is a prevalent medical emergency in primary emergency care settings. Triage of chest pain prior to hospital admission presents significant challenges due to the absence of sufficiently sensitive diagnostic tools. Clinical signs, symptoms, risk assessment scores, or a normal electrocardiogram (ECG) can reliably exclude acute myocardial infarction (MI). This diagnostic uncertaint…

Not Yet Recruiting

NCT07689162 — Liposomal Bupivacaine vs Standard Bupivacaine for Post-Rhinoplasty Analgesia

StatusNot yet recruiting
PhasePhase 2
SponsorWashington University School of Medicine
Enrollment45
Study TypeINTERVENTIONAL
ConditionsPain, Postoperative
Interventions;

The purpose of our study is to find out which pain medication is more effective in reducing pain after nose surgery(rhinoplasty). We are looking to find the best treatment to reduce discomfort and improve the healing process for patients having nose surgery.

NCT07691359 — Osteoporotic Fracture and Lidocaine Plaster 5% for Neuropathic Pain preventioN

StatusNot yet recruiting
PhasePhase 4
SponsorUniversity Hospital, Clermont-Ferrand
Enrollment30
Study TypeINTERVENTIONAL
ConditionsOsteoporotic 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 …

NCT07691385 — Prevention of Pain Induced During Bed Bath in Ehpad

StatusNot yet recruiting
PhaseN/A
SponsorHôpital NOVO
Enrollment12
Study TypeINTERVENTIONAL
ConditionsGeriatric Care
Interventions;

Residents of long-term care facilities are subjected to procedures and treatments that may be painful. The prevalence is 90% among older adults living in institutions. Preventing procedure-induced pain is essential, as the consequences can be even more harmful. Induced pain is defined as “short-term pain caused by a healthcare provider, treatment, or care, under predictable circumstances,” acco…

NCT07504601 — Investigating the Analgesic Potential of (2R,6R)-HNK in Acute Pain in Healthy Volunteers

StatusNot yet recruiting
PhasePhase 2
SponsorNational Center for Complementary and Integrative Health (NCCIH)
Enrollment92
Study TypeINTERVENTIONAL
ConditionsHealthy Volunteers
Interventions;

Background:

Opioid drugs are often prescribed for acute and chronic pain. But these drugs are addictive, and they lead to more than 14,000 overdose deaths in the United States each year. Researchers want to find new drugs that relieve pain but are not addictive. This study will test whether a single dose of an experimental drug called (2R,6R)-hydroxynorketamine (HNK) can help reduce short term…

NCT07689448 — Preoperative Versus Postoperative Interscalene Block in Arthroscopic Rotator Cuff Repair

StatusNot yet recruiting
PhaseN/A
SponsorIstinye University
Enrollment42
Study TypeOBSERVATIONAL
ConditionsRotator Cuff Tear Repair; Interscalene Blocks; Rotator Cuff Tears

This study is evaluating whether the timing of an interscalene nerve block affects pain control and recovery after arthroscopic rotator cuff repair surgery.

An interscalene block is commonly used to reduce pain after shoulder surgery. However, it is not known whether administering the block before surgery or after surgery provides better outcomes. Participants undergoing arthroscopic rotator c…

NCT07549490 — Human Experimental Models of Pain (HEMP)

StatusNot yet recruiting
PhaseN/A
SponsorNational Center for Complementary and Integrative Health (NCCIH)
Enrollment25
Study TypeINTERVENTIONAL
ConditionsAcute Pain
Interventions; ;

This pilot study will test an innovative way to establish how pain medicines provide analgesia in healthy adults. The study uses a group of short, controlled pain tests to look at different types of pain responses in the body. The main goal is to find out if this testing approach can show the pain-relieving effects of 2 medicines, pregabalin and naproxen versus placebo, and show how they provid…

NCT07035119 — Transcranial Magnetic Stimulation for Chronic Scrotal Content Pain

StatusNot yet recruiting
PhasePhase 1 / Phase 2
SponsorMedical University of South Carolina
Enrollment50
Study TypeINTERVENTIONAL
ConditionsScrotal Pain
Interventions

The purpose of this study is to perform an open label feasibility trial of TMS for the treatment of chronic scrotal content pain.

NCT07689955 — A Phase-II Clinical Trial of Radiotherapy to the Coeliac Plexus to Help Pain in Advanced Pancreatic Cancer

StatusNot yet recruiting
PhasePhase 2
SponsorRoyal Marsden NHS Foundation Trust
Enrollment52
Study TypeINTERVENTIONAL
ConditionsPancreatic Cancer
Interventions

Pain from advanced pancreatic cancer is often difficult to control. This pain commonly occurs when the cancer affects a network of nerves in the abdomen called the coeliac plexus. Even strong pain medicines, including morphine and related drugs, may not give enough relief. Some patients may have a procedure called a coeliac plexus block, but this is invasive, not widely available, and does not …

NCT07607223 — Acupuncture for Heel Pain Syndrome

StatusNot yet recruiting
PhaseN/A
SponsorFirst Teaching Hospital of Tianjin University of Traditional Chinese Medicine
Enrollment150
Study TypeINTERVENTIONAL
ConditionsHeel Pain Syndrome
Interventions; ;

The main goal of this study is to determine whether acupuncture at the Heel Pain Point, a distal acupuncture point located on the palm, is an effective and safe treatment for heel pain syndrome. This randomized controlled trial compares Heel Pain Point acupuncture with manual therapy and sham acupuncture to evaluate both clinical efficacy and functional recovery. Specifically, the researchers a…

NCT07566312 — Study of QL Analgesic Response and Extent

StatusNot yet recruiting
PhasePhase 4
SponsorDuke University
Enrollment25
Study TypeINTERVENTIONAL
ConditionsAcute Pain; Postoperative Pain; Regional Anesthesia Block
Interventions

A total of 14-18 healthy volunteers will be included. There will be three different procedure days, separated by at least one week. On each visit, the subjects will receive a QL block, according to the randomization process. Each volunteer will undergo pre-procedure screening on the first visit. The blocks will be performed on the same side, by the same anesthesiologist, with at least one week …

Completed Trials

NCT01862731 — Muscle Strength Loss and Its Effect on Knee Cap Motion in Volunteers With Anterior Knee Pain

StatusCompleted
PhaseN/A
SponsorNational Institutes of Health Clinical Center (CC)
Enrollment35
Study TypeOBSERVATIONAL
ConditionsPatellofemoral Pain Syndrome

Background:

- Researchers are interested in how the muscles affect the movement of the knee cap. These muscles may be related to different kinds of knee pain that are not caused by an injury or a disease. Imaging studies such as magnetic resonance imaging (MRI) can be used to look at these muscles. To study these muscles and how they move, researchers will use MRI to look at healthy individua…

NCT02822989 — Using the Cholinergic Anti-Inflammatory Pathway to Treat Systemic Lupus Musculoskeletal Pain

StatusCompleted
PhaseN/A
SponsorNorthwell Health
Enrollment19
Study TypeINTERVENTIONAL
ConditionsLupus Erythematosus, Systemic; Musculoskeletal Pain
Interventions;

Systemic Lupus Erythematosus (SLE) is a chronic autoimmune, inflammatory disease and musculoskeletal pain is one of the most common symptoms. This study will investigate whether transcutaneous stimulation of the vagus nerve will decrease lupus musculoskeletal pain. This study will additionally investigate the biologic effects of vagus nerve stimulation on inflammation. It will be the first clin…

NCT04442425 — Machine Learning to Analyze Facial Imaging, Voice and Spoken Language for the Capture and Classification of Cancer/Tumor Pain

StatusCompleted
PhaseN/A
SponsorNational Cancer Institute (NCI)
Enrollment83
Study TypeOBSERVATIONAL
ConditionsCancer; Neoplasms; Solid Tumors

Background:

Cancer pain can have a very negative effect on people s daily lives. Researchers want to use machine learning to detect facial expressions and voice signals. They want to help people with cancer by creating a model to measure pain. They want the model to reflect diverse faces and facial expressions.

Objective:

To find out whether facial recognition technology can be used to class…

NCT04543097 — Work And Vocational advicE Study - Effectiveness of Adding a Brief Vocational Support Intervention to Usual Primary Care

StatusCompleted
PhaseN/A
SponsorKeele University
Enrollment130
Study TypeINTERVENTIONAL
ConditionsMusculoskeletal Pain; Mental Health Issue; Mental Health Disorder; Other Physical Health Condition; Absence
Interventions

Maintaining the population’s fitness for work is a priority for the UK Government. People with poor health often struggle at work and take sick leave. Work brings financial, social and health benefits. Few employees receive support to manage their health at work, known as vocational advice, so when their health affects work they visit their general practitioner (GP). The investigators have rece…

StatusCompleted
PhaseN/A
SponsorRutgers University
Enrollment36
Study TypeINTERVENTIONAL
ConditionsHIV 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.

NCT07689617 — Ultrasound-Guided Intermediate Cervical Plexus Block for Postoperative Analgesia in Vagus Nerve Stimulation Surgery

StatusCompleted
PhaseN/A
SponsorFirat University
Enrollment52
Study TypeINTERVENTIONAL
ConditionsDrug-Resistant Epilepsy; Epilepsy; Vagus Nerve Stimulation
Interventions; ;

This prospective, randomized, double-blind, placebo-controlled clinical trial aims to evaluate the analgesic efficacy of ultrasound-guided intermediate cervical plexus block (ICB) in patients undergoing vagus nerve stimulation (VNS) implantation surgery under general anesthesia. Participants are randomly assigned to receive either an ultrasound-guided ICB with 10 mL of 0.25% bupivacaine or a pl…

NCT07689370 — Buzzy® and Cognitive Behavioral Intervention Package During Blood Draw in Children

StatusCompleted
PhaseN/A
SponsorKocaeli University
Enrollment180
Study TypeINTERVENTIONAL
ConditionsProcedural Pain; Procedural Fear; Procedural Anxiety
Interventions;

This study evaluated the effects of Buzzy® and a Cognitive Behavioral Intervention Package on pain and fear/anxiety during blood draw in children aged 7-12 years. Blood draw is a common procedure in children, but it may cause pain, fear, and anxiety. Non-pharmacological methods may help children cope better with this procedure.

Children were randomly assigned to one of three groups: a control …

NCT06983600 — The Effect of SuJok Application on Dysmenorrhea and Quality of Life in Young People With Primary Dysmenorrhea:

StatusCompleted
PhaseN/A
SponsorMuş Alparslan University
Enrollment100
Study TypeINTERVENTIONAL
ConditionsDysmenorrhea (Disorder); Alternative Treatment
Interventions

Menarche, which is one of the most prominent features of maturation in adolescents and the transition from childhood to adulthood, causes many problems. The most prominent of these complaints is dysmenorrhea. Primary dysmenorrhea, the most common form of dysmenorrhea, is a gynecological disorder characterized by pain that starts in the lower abdomen before or during menstruation and radiates to…

NCT06839313 — Comparison of Hypericum Perforatum, Topical Corticosteroids, and Hyaluronic Acid for Recurrent Aphthous Stomatitis

StatusCompleted
PhaseN/A
SponsorBatman University
Enrollment75
Study TypeINTERVENTIONAL
ConditionsStomatitis, Aphthous
Interventions; ;

Recurrent aphthous stomatitis (RAS) is one of the most common ulcerative diseases of the oral mucosa and is characterized by recurrent painful ulcers that adversely affect eating, speaking, and overall quality of life. Although several topical agents are available to relieve symptoms and promote healing, no definitive treatment has yet been established.

This randomized prospective study was de…

NCT06722014 — Integrating Pain-CBT Into an mHealth Analgesic Support Intervention for Patients With Chronic Pain From Advanced Cancers

StatusCompleted
PhaseN/A
SponsorDana-Farber Cancer Institute
Enrollment64
Study TypeINTERVENTIONAL
ConditionsPain; Pain Syndrome; Advanced Cancer
Interventions;

Smartphone Technology to Alleviate Malignant Pain (STAMP) + Cognitive Behavioral Therapy for Pain (STAMP+CBT) The purpose of the study is to develop and refine the mHealth pain-CBT app intervention and carry out a randomized pilot to test the novel mHealth (Mobile health technology) intervention, which harmonizes psychological and pharmacological support for advanced cancer pain.

The name of t…

NCT07689916 — Machine Learning-Based Risk Identification and Precision Exercise for Common Running Injuries

StatusCompleted
PhaseN/A
SponsorZeyi Zhang
Enrollment204
Study TypeINTERVENTIONAL
ConditionsRunning-related Injuries; Medial Tibial Stress Syndrome; Patellofemoral Pain, PFP; Chronic Achilles Tendinopathy
Interventions;

This study aims to identify biomechanical risk factors associated with common running-related injuries in recreational runners using machine learning analysis. It also aims to evaluate whether a precision exercise intervention based on these risk factors can improve injury-related biomechanical and kinematic outcomes.

The main questions it aims to answer are:

Which biomechanical features iden…

NCT07639918 — Effect of Kinesio-taping With Routine Physical Therapy in Wrist Joint Hypermobility

StatusCompleted
PhaseN/A
SponsorUniversity of Lahore
Enrollment38
Study TypeINTERVENTIONAL
ConditionsWrist Joint Hypermobility
Interventions;

The study will be randomized controlled trial. This study will be conducted at the University of Lahore Teaching Hospital, Lahore, Pakistan. This will investigate the effects of routine physical therapy with and without Kinesio taping in patients with Wrist Joint Hypermobility. A sample size of 38 participants will be randomly assigned into two groups. Group A will receive routine physical ther…

NCT07686627 — ShotBlocker and Warm Gel Pack During Neonatal Heel Prick (HEAL)

StatusCompleted
PhaseN/A
SponsorMarmara University
Enrollment147
Study TypeINTERVENTIONAL
ConditionsProcedural Pain; Heel Prick; Newborn
Interventions;

This study evaluated the effects of ShotBlocker and a warm gel pack on pain, comfort, and physiological parameters during heel prick testing in healthy term newborns. A three-arm randomized controlled trial was conducted at a city hospital between October 2025 and May 2026. Newborns were randomly assigned to the ShotBlocker group, warm gel pack group, or routine care group. Pain was assessed us…

NCT06983093 — Effects of Rain Stick and Musical Egg on Pain, Fear and Anxiety

StatusCompleted
PhaseN/A
SponsorHakkari Universitesi
Enrollment120
Study TypeINTERVENTIONAL
ConditionsProcedural Pain; Procedural Anxiety; Fear Needles
Interventions;

This research will be conducted in a pre-test-post-test parallel group randomized controlled experimental study model to determine the effects of rain stick and musical egg applied during blood collection on pain, fear and anxiety in children aged 4-6.

Research Hypotheses H1: The mean pain scores of the children in the rain stick group are lower than the mean scores of the children in the cont…

StatusCompleted
PhaseN/A
SponsorUniversite de Picardie Jules Verne
Enrollment26
Study TypeINTERVENTIONAL
ConditionsPain-related Fear; Kinesiophobia (Fear of Movement); Movement-Related Threat
Interventions;

The goal of this clinical trial is to learn how experimentally induced movement-related threat affects emotional, autonomic, and motor responses in healthy adults. The main questions it aims to answer are:

  • Does movement-related threat change walking performance or upper-limb pointing movements?
  • Are these effects moderated by participants’ level of kinesiophobia?
  • Does movement-related thr…

NCT07327827 — Comparative Effects of Back School Based Intervention Versus Cranio-Cervical Muscle Training in Computer Users With Cervicogenic Headache

StatusCompleted
PhaseN/A
SponsorLahore University of Biological and Applied Sciences
Enrollment44
Study TypeINTERVENTIONAL
ConditionsCervicogenic Headache
Interventions;

The aim of the study is to compare Back School Based Intervention with Cranio- Cervical muscle training in participants with Cervicogenic headache. The study wants to investigate that which intervention helps to mange pain, improve posture and reduce disability. The study aims to answer the question:

  • How effective is Back School Based intervention on pain, posture and disability in computer …

NCT07335822 — The Effectiveness of Low-Level Laser Therapy in the Treatment of Meralgia Paresthetica

StatusCompleted
PhaseN/A
SponsorIstanbul Training and Research Hospital
Enrollment36
Study TypeINTERVENTIONAL
ConditionsMeralgia 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…

NCT07691151 — Targeted Cervical Versus Integrated Trunk and Diaphragmatic Muscle Retraining for Chronic Mechanical Neck Pain

StatusCompleted
PhaseN/A
SponsorGulf Medical University
Enrollment40
Study TypeINTERVENTIONAL
ConditionsChronic Mechanical Neck Pain; Neck Pain
Interventions;

Persistent pain, functional disability, cervical motor control deficit, and abnormal posture are associated with chronic mechanical neck pain. This study aimed to evaluate the efficacy of an integrated physiotherapy program of cervical motor control training, lumbopelvic stabilization, diaphragmatic breathing exercises, and pressure biofeedback versus conventional cervical physiotherapy in pati…