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 Nail Diseases from the ClinicalTrials.gov database.
Trial Summary
- Total studies: 50
- Recruiting: 13
- Active, not recruiting: 8
- Completed: 16
- Other: 13
Results are refreshed periodically and may not reflect the most current information available from ClinicalTrials.gov.
Recruiting Trials
NCT03823534 — Post-Op Pain Control for Prophylactic Intramedullary Nailing.
| Status | Recruiting |
| Phase | Phase 3 |
| Sponsor | St. Louis University |
| Enrollment | 60 |
| Study Type | INTERVENTIONAL |
| Conditions | Bone Metastases; Lymphoma; Multiple Myeloma; Opioid Use; Pain |
| Interventions | ; ; |
Nationally, the opioid crisis has become a major epidemic with increasing mortality rates each year. Orthopedic surgeons routinely prescribe narcotics instead of NSAIDs for post-op pain control because of risk of delayed healing and nonunion due to NSAID use. Orthopedic oncology, however, has a unique subset of patients that undergo prophylactic placement of intramedullary femoral nails. Becaus…
NCT07006675 — Effect of NSAIDs on Union, Opioid Utilization and Pain Management for Tibia Fractures: A Pragmatic, Randomized Controlled Trial
| Status | Recruiting |
| Phase | Phase 3 |
| Sponsor | Major Extremity Trauma Research Consortium |
| Enrollment | 1000 |
| Study Type | INTERVENTIONAL |
| Conditions | Tibial Fractures; Pain |
| Interventions |
Two arm, pragmatic, randomized controlled multicenter Phase III noninferiority trial evaluating the efficacy of standard pain management without NSAIDs (Group 1) vs. standard pain management plus up to 6 weeks of NSAIDs (Group 2) in the treatment of tibial shaft fractures.
NCT04950218 — Prevalence and Risk Factors asSOciated With CArdiac comorbiDIty in psoriAsis
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Herlev and Gentofte Hospital |
| Enrollment | 1000 |
| Study Type | OBSERVATIONAL |
| Conditions | Psoriasis; Cardiovascular Diseases; Cardiovascular Risk Factor; Cardiovascular Pathology; Psoriasis Vulgaris |
In a prospective cohort study (n = 1.000), the investigators aim to investigate the correlation between cardiac biomarkers and advanced echocardiography and determine whether these are prognostic markers of heart disease in patients suffering from psoriasis.
NCT04868305 — Intramedullary Nail Versus Hip Arthroplasty in Unstable Trochanteric Hip Fractures
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Helse Stavanger HF |
| Enrollment | 170 |
| Study Type | INTERVENTIONAL |
| Conditions | Hip Injuries and Disorders; Hip Fractures |
| Interventions | ; |
A hip fracture is a large burden to the patient with increased mortality, pain and increased need for daily assistance. Trochanteric fractures of the femur (FTF) represents about 35% of the hip fractures. Today FTFs are mainly treated with internal fixation using sliding hips screws (SHS) or intramedullary nail (IMN), whilst hip arthroplasty (THA/HA) is rarely used. Despite advances in the desi…
NCT05639933 — Study to Investigate the Efficacy, Safety, and Tolerability of Topical HT-001 for the Treatment of Skin Toxicities Associated With Epidermal Growth Factor Receptor Inhibitors
| Status | Recruiting |
| Phase | Phase 2 |
| Sponsor | Hoth Therapeutics, Inc. |
| Enrollment | 152 |
| Study Type | INTERVENTIONAL |
| Conditions | Acneiform Eruption Due to Chemical; Xerosis Cutis; Paronychia |
| Interventions | ; ; |
The goal of this clinical trial is to learn about HT-001 Topical Gel for treatment of EGFR inhibitor-induced skin toxicities. The main questions it aims to answer are:
- Determine the therapeutic effect of HT-001 for treatment of patients who develop acneiform rash undergoing Epidermal Growth Factor inhibitor (EGFRI) therapy using the acneiform rash investigator’s global assessment scale [ARI…
NCT06156384 — Study to Assess the Pain, Satisfaction, and Quality of Life of Patients With FITBONE® Lengthening Nail
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Orthofix s.r.l. |
| Enrollment | 45 |
| Study Type | OBSERVATIONAL |
| Conditions | Leg Length Inequality |
| Interventions |
This study is a prospective observational non-interventional multi-centre cohort study of patients, 12 years or older, initiating a lower limb lengthening procedure with FITBONE and who have a length discrepancy of 30mm or more between the limbs.
The following parameters will be assessed for up to 24 months.
- Pain using the Visual Analog Scale (VAS), Patient Global Assessment (PGA) and Clini…
NCT06327295 — A Study of ATB1651 in Adults With Mild to Moderate Onchomycosis
| Status | Recruiting |
| Phase | Phase 2 |
| Sponsor | AmtixBio Co., Ltd. |
| Enrollment | 120 |
| Study Type | INTERVENTIONAL |
| Conditions | Onychomycosis |
| Interventions | ; ; |
The study is designed to evaluate the Safety, Tolerability and Pharmacokinetics of ATB1651 in participants with mild to moderate onychomycosis
NCT06485505 — Isotretinoin Versus Excimer Light an Adjuvant in Treating Onychomycosis
| Status | Recruiting |
| Phase | Phase 1 |
| Sponsor | Zagazig University |
| Enrollment | 36 |
| Study Type | INTERVENTIONAL |
| Conditions | Onychomycosis |
| Interventions | ; ; |
3 groups of patients with onychomycosis will be recruited. Group A will receive itraconazole alone. Group B will receive itraconazole + low dose isotretinoin and group C will be treated with itraconazole + excimer light sessions.
NCT06643416 — Efficacy and Safety of Add-on Timolol for EGFR-TKI and ALK-TKI Induced Paronychia
| Status | Recruiting |
| Phase | Phase 3 |
| Sponsor | Queen Mary Hospital, Hong Kong |
| Enrollment | 40 |
| Study Type | INTERVENTIONAL |
| Conditions | Paronychia; EGFR-TKI; ALK-TKI |
| Interventions | ; |
To assess the clinical efficacy of add-on topical timolol 0.5% eye drops to betamethasone valerate 0.1% for the treatment of EGFR-TKI and ALK-TKI induced paronychia.
NCT06689852 — CLINICAL INVESTIGATION FOR THE EVALUATION OF EFFICACY AND SAFETY OF TWO PRODUCTS FOR THE TREATMENT OF ONYCHOMYCOSIS
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Oystershell NV |
| Enrollment | 88 |
| Study Type | INTERVENTIONAL |
| Conditions | Onychomycosis |
| Interventions | ; |
The efficacy and safety of ENRICHED (X92001591) will be evaluated in a multicentric, randomized, evaluator blinded clinical investigation in 88 patients.
NCT06861023 — Review of the Literature and Serie of Patients Who Underwent Reconstruction After Wide Local Excision of Nail Apparatus for Melanoma
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Centre Hospitalier Universitaire de Nice |
| Enrollment | 10 |
| Study Type | OBSERVATIONAL |
| Conditions | Melanoma |
| Interventions |
Melanomas of the nail bed are often diagnosed at the locally advanced stage. The standard treatment was amputation of the finger or toe, but it has now been established that enlarged excision of the nail plate is sufficient under certain conditions. Reconstruction of the nail system can be performed by several techniques. Here, the investigators present a series of patients reconstructed by INT…
NCT07547241 — Comparison of Two Surgical Methods (Winograd vs. Sleeve Method) in the Treatment of Ingrown Toenail.
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Pakistan Institute of Medical Sciences |
| Enrollment | 312 |
| Study Type | INTERVENTIONAL |
| Conditions | Ingrown Toenail (Onychocryptosis) |
| Interventions | ; |
This randomized clinical trial aims to compare the recurrence rates of two surgical techniques-Winograd procedure and sleeve (gutter) method-in the treatment of ingrown toenails (onychocryptosis). A total of 312 nails will be randomized into two groups, with patients receiving either the Winograd procedure or sleeve method. Participants will be followed for 30 days post-intervention to assess r…
NCT07029516 — Study to Assess Efficacy, Safety and Tolerability of a Nail Patch in Patients With Nail Fragility, Mychosis, Psoriasis
| Status | Recruiting |
| Phase | Phase 3 |
| Sponsor | Wooshin Labottach Co., Ltd. |
| Enrollment | 72 |
| Study Type | INTERVENTIONAL |
| Conditions | Nail Psoriasis; Nail Damage; Mycosis |
| Interventions | ; |
A randomized, double blind, placebo-controlled, unicenter, parallel group study to assess the efficacy, safety and tolerability of a multi-funtion toe nail patch in patients affected by nail fragility, nail mychosis and psoriasis 72 patients in 6 subgroups Treatment duration 3 months + 1 month follow-up
Active, Not Recruiting
NCT02530177 — Study of Chemotherapy-Induced Hair Changes and Alopecia, Skin Aging and Nail Changes in Women With Non-Metastatic Breast Cancer
| Status | Active, not recruiting |
| Phase | N/A |
| Sponsor | Memorial Sloan Kettering Cancer Center |
| Enrollment | 546 |
| Study Type | OBSERVATIONAL |
| Conditions | Non-Metastatic Breast Cancer |
| Interventions | ; ; |
The purpose of this study is to see how many patients develop hair, skin and nail changes due to cancer treatments. The investigators would like to study the clinical factors, genetic markers, and impact on patients’ health-related quality of life to learn more about who is at greater risk. We trust that the study will improve our understanding of how cancer patients feel about their skin, hair…
NCT05621369 — Psorcast Mobile Study
| Status | Active, not recruiting |
| Phase | N/A |
| Sponsor | Sage Bionetworks |
| Enrollment | 1000 |
| Study Type | OBSERVATIONAL |
| Conditions | Psoriatic Arthritis; Psoriasis; Psoriatic Conditions; Dermatologic Disease; Rheumatologic Disease |
| Interventions | ; ; |
The purpose of this study is to understand variation in the symptoms of psoriasis and psoriatic arthritis using simple, scalable smartphone-based measurements. This study uses an iPhone app to record these symptoms through questionnaires and sensors.
NCT05408546 — Novel α2-Antiplasmin Inactivation for Lysis of Intravascular Thrombi (NAIL-IT) Trial
| Status | Active, not recruiting |
| Phase | Phase 2 |
| Sponsor | Translational Sciences, Inc. |
| Enrollment | 64 |
| Study Type | INTERVENTIONAL |
| Conditions | Pulmonary Embolism |
| Interventions | ; |
Phase II trial of TS23
NCT05938361 — Efficacy of Tildrakizumab in Difficult-to-treat Areas in Psoriasis
| Status | Active, not recruiting |
| Phase | N/A |
| Sponsor | Clin4all |
| Enrollment | 120 |
| Study Type | OBSERVATIONAL |
| Conditions | Psoriasis Palmaris; Psoriasis Genital; Psoriasis of Scalp; Psoriasis Plantaris; Psoriasis Nail |
| Interventions | ; ; |
Psoriasis is a chronic inflammatory disease that affects between 2% and 4% of the French population.Some specific localizations are more difficult to manage, such as the scalp, nails, genital region and palmoplantar localizations.
Tildrakizumab, an anti-interleukin-23 (IL-23) monoclonal antibody, has demonstrated efficacy and safety in the treatment of patients with moderate to severe psoriasi…
NCT06777212 — Mindfulness Intervention for Psychological and Family Dynamics in Children with Body-Focused Repetitive Behaviors
| Status | Active, not recruiting |
| Phase | N/A |
| Sponsor | Children’s Hospital of Fudan University |
| Enrollment | 200 |
| Study Type | INTERVENTIONAL |
| Conditions | Mindfulness Skills; Psychosocial Education |
| Interventions | ; |
This is a single-center, randomized, controlled intervention study designed to evaluate the effectiveness of mindfulness intervention on reducing body-focused repetitive behaviors (BFRBs) in children aged 8-18, such as nail-biting, skin-picking, and hair-pulling. Participants will be randomly assigned to either a mindfulness intervention group or a psychosocial education control group. The stud…
NCT07012343 — Exploring Different Dose-frequency Home Photodynamic Therapy Protocols Using a Novel Home-targeted LED Device for Onychomycosis
| Status | Active, not recruiting |
| Phase | N/A |
| Sponsor | Chulalongkorn University |
| Enrollment | 50 |
| Study Type | INTERVENTIONAL |
| Conditions | Onychomycosis of Toenails; Onychomycosis of Fingernail |
| Interventions | ; |
This randomized feasibility trial aims to determine the optimal light energy dose and treatment frequency for home-based photodynamic therapy (hPDT) using a novel LED device (L-Home PhoD) for the treatment of onychomycosis.
NCT07065773 — Safety, Tolerability and Efficacy of Trichostatin A in Patients With Mild to Severe Onychomycosis
| Status | Active, not recruiting |
| Phase | Phase 2 |
| Sponsor | Vanda Pharmaceuticals |
| Enrollment | 50 |
| Study Type | INTERVENTIONAL |
| Conditions | Onychomycosis of Toenail |
| Interventions |
This is a multicenter, open label study designed to evaluate the safety, tolerability, and efficacy of topically administered VTR-297 solution. The efficacy objectives of the study will be assessed using fungal culture testing, Neutral Red Staining (NRS) microscopy examination, and KOH microscopy examination after 4 weeks of treatment with VTR-297.
NCT07039357 — Reconfirming the Safety and Performance of the Glyconics-DS System in Known Populations With and Without Diabetes
| Status | Active, not recruiting |
| Phase | N/A |
| Sponsor | Glyconics Ltd |
| Enrollment | 100 |
| Study Type | INTERVENTIONAL |
| Conditions | Diabetes Mellitus; Healthy |
| Interventions |
A single-site, open label, confirmatory study assessing two biomarkers indicative of levels of glycaemia; glycated keratin in fingernails and glycated haemoglobin (HbA1c). Screening for diabetes
Not Yet Recruiting
NCT06696612 — Dermoscopy in Nails
| Status | Not yet recruiting |
| Phase | N/A |
| Sponsor | Assiut University |
| Enrollment | 50 |
| Study Type | OBSERVATIONAL |
| Conditions | Vitiligo; Healthy |
| Interventions |
Study types and frequency of nail changes in patients with vitiligocompared to healthy subjects
NCT06790940 — Construction of a Psoriasis and Psoriatic Arthritis Diagnostic Model Based on Multidimensional Nail Information
| Status | Not yet recruiting |
| Phase | N/A |
| Sponsor | Shanghai Yueyang Integrated Medicine Hospital |
| Enrollment | 310 |
| Study Type | OBSERVATIONAL |
| Conditions | Psoriasis (PsO); Psoriatic Arthritis; Palmoplantar Pustulosis (PPP); Plaque Psoriasis |
| Interventions |
Psoriasis is a globally prevalent chronic relapsing skin disease, characterized by its long duration and tendency to relapse. In addition to skin symptoms, it can also affect nails and joints, leading to pathological features such as pitting, leukonychia, red lunula, or severe nail dystrophy. Some patients with psoriasis may develop psoriatic arthritis. Psoriatic arthritis (PsA) is a chronic re…
NCT06802848 — Real-World Study of Xeligekimab for Moderate to Severe Plaque Psoriasis(XP-Real)
| Status | Not yet recruiting |
| Phase | N/A |
| Sponsor | Chongqing Genrix Biopharmaceutical Co., Ltd |
| Enrollment | 1000 |
| Study Type | OBSERVATIONAL |
| Conditions | Plaque Psoriasis; Psoriatic Arthritis; Scalp Psoriasis; Nail Psoriasis; Palmoplantar Psoriasis |
| Interventions |
Xeligekimab Injection was approved in China on August 20, 2024, for treating adults with moderate to severe plaque psoriasis who are candidates for systemic treatment or phototherapy. Despite the promising efficacy and safety shown in the phase III clinical trial, real-world data is needed to further support clinical decisions for this patient group. This study aims to evaluate the effectivenes…
NCT06862232 — P : Ingrown Toenail Patient I : Bird Flap Surgery C : Noel Winograd Method O : Recurrence, Complications, Functional Outcome, Pain,
| Status | Not yet recruiting |
| Phase | N/A |
| Sponsor | Kutahya City Hospital |
| Enrollment | 108 |
| Study Type | INTERVENTIONAL |
| Conditions | Ingrown Toenail |
| Interventions | ; ; |
The treatment of ingrown toenails is highly diverse, with numerous surgical techniques described in the literature alongside conservative approaches. The primary goals of all these surgical methods are to reduce recurrence rates, improve patients’ quality of life, and achieve favorable cosmetic outcomes. In this study, we aim to compare the recently introduced Bird Flap, a modified Winograd tec…
NCT06812195 — Periprosthetic Plate Over Humeral Nail
| Status | Not yet recruiting |
| Phase | N/A |
| Sponsor | Assiut University |
| Enrollment | 3 |
| Study Type | INTERVENTIONAL |
| Conditions | Osteopenia, Osteoporosis |
| Interventions |
use of plate over humeral nail in deformity correction of femur in adult osteoporotic bone
NCT06971341 — Study in Patients With Onychomycosis Treated With Mycoclear® and Ciclopirox
| Status | Not yet recruiting |
| Phase | N/A |
| Sponsor | University of Bologna |
| Enrollment | 80 |
| Study Type | OBSERVATIONAL |
| Conditions | Onychomycosis of Toenails |
The goal of this study is to learn about the effectiveness and safety of two products, ciclopirox or Mycoclear®, in treating fungal infections. People with fungal infections of the nails and over the age of 18 were treated at the Department of Dermatology, IRCCS Azienda Ospedaliero - Universitaria Sant’Orsola in Bologna (Italy) between January 1, 2019, and April 30, 2023. The people were treate…
NCT07033962 — Fractional CO₂ Laser or 40% Urea With Topical Fluconazole Microemulsion in Onychomycosis
| Status | Not yet recruiting |
| Phase | N/A |
| Sponsor | Assiut University |
| Enrollment | 40 |
| Study Type | INTERVENTIONAL |
| Conditions | Onychomycosis |
| Interventions | ; |
To evaluate the efficacy and safety of topical fluconazole microemulsion enhanced by fractional CO₂ laser versus by 40% urea ablation in treatment of Onychomycosis.
NCT07214116 — Virtual Reality, Music, and Education to Reduce Anxiety in Patients Undergoing Ingrown Toenail Surgery
| Status | Not yet recruiting |
| Phase | N/A |
| Sponsor | University of Seville |
| Enrollment | 175 |
| Study Type | INTERVENTIONAL |
| Conditions | Ingrown Toenail |
| Interventions | ; ; |
The main objective of this clinical trial is to evaluate whether watching an educational video before surgery, combined with the use of virtual reality or music during surgery, can reduce anxiety and pain in people undergoing ingrown toenail (onychocryptosis) surgery.
The main questions the study aims to answer are:
Are the educational video, virtual reality, and music effective in controllin…
NCT07546032 — Clinical Study on the Medical Device PROXERA PSOMED 30 for the Treatment of Nail Psoriasis: Evaluation of Safety and Efficacy
| Status | Not yet recruiting |
| Phase | N/A |
| Sponsor | ICIM International S.r.l. |
| Enrollment | 21 |
| Study Type | INTERVENTIONAL |
| Conditions | Nail Psoriasis |
| Interventions |
The purpose of this interventional clinical study is to evaluate the safety and efficacy of PROXERA PSOMED 30, a topical medical device containing 30% urea, for the treatment of nail psoriasis in adults with nail psoriasis. The primary question the study aims to answer is whether PROXERA PSOMED 30 improves the clinical signs of nail psoriasis more effectively than a control treatment (Vaseline)…
NCT06545695 — Epidermal Growth Factor Receptor Inhibition for Keratinopathies
| Status | Not yet recruiting |
| Phase | Phase 1 / Phase 2 |
| Sponsor | Northwestern University |
| Enrollment | 44 |
| Study Type | INTERVENTIONAL |
| Conditions | Epidermolytic Ichthyosis; Palmoplantar Keratoderma; Pachyonychia Congenita |
| Interventions |
Epidermal growth factor receptor (EGFR) signaling plays a key role in regulating epidermal cell proliferation, survival, and differentiation. Keratins form a scaffold with epidermal desmosomes that involves ErbB/ EGFR signaling and keratin deficiency makes keratinocytes more sensitive to EGFR activation. Erlotinib, an EGFR inhibitor, was approved 20 years ago for cancer treatment and is general…
Enrolling by Invitation
NCT07127952 — Correlations of the Microvascular Abnormalities on NVC (Nail Fold Video Capillaroscopy) and GAVE (Gastric Antral Vascular Ectasia) as Seen on EGD
| Status | Enrolling by invitation |
| Phase | N/A |
| Sponsor | Mayo Clinic |
| Enrollment | 75 |
| Study Type | INTERVENTIONAL |
| Conditions | Gastric Antral Vascular Ectasia |
| Interventions |
The purpose of this research is to determine whether a procedure called capillaroscopy can help distinguish patients who are diagnosed with GAVE (gastric antral vascular ectasia) with an autoimmune disease versus idiopathic/other conditions based on EGD findings.
Completed Trials
NCT00233493 — Spread of Dermatophytes Among Families
| Status | Completed |
| Phase | N/A |
| Sponsor | University Hospitals Cleveland Medical Center |
| Enrollment | 50 |
| Study Type | OBSERVATIONAL |
| Conditions | Onychomycosis; Tinea Pedis |
The objective is to demonstrate person-to-person spread of dermatophytes of the skin and nails among family members, as measured by fungal culture and DNA typing of the dermatophytes isolated.
NCT02283983 — Evaluation of Cryoprotection Induced Nail Toxicity Docetaxel Low Cumulative Dose
| Status | Completed |
| Phase | N/A |
| Sponsor | Centre Hospitalier Departemental Vendee |
| Enrollment | 319 |
| Study Type | INTERVENTIONAL |
| Conditions | Breast Neoplasms |
| Interventions | ; |
For the specific patient population studied receiving 5-Fluorouracil, epirubicin and cyclophosphamide - Docetaxel sequence (cumulative dose <300 mg / m2), using a cryoprotection has never been assessed.
The effectiveness of cryoprotection of onycholysis secondary to Docetaxel is not well established in this population (breast cancer in the adjuvant setting) and is based solely on a publicatio…
NCT03098342 — Comparison of Efficacy and Safety Between Methylene Blue-mediated Photodynamic Therapy and 5% Amorolfine Nail Lacquer for Toenail Onychomycosis Treatment
| Status | Completed |
| Phase | N/A |
| Sponsor | Chulalongkorn University |
| Enrollment | 27 |
| Study Type | INTERVENTIONAL |
| Conditions | Onychomycosis of Toenail |
| Interventions | ; |
Study centre and address
King Chulalongkorn Memorial Hospital
Primary objective
To compare the efficacy and the safety of methylene blue-mediated photodynamic therapy and 5% amorolfine nail lacquer for toenail onychomycosis in Asians
NCT03504462 — Feasibility of Specific Anesthesia of the Forefoot Preserving the Sensitivity of the Heel for Foot Surgery
| Status | Completed |
| Phase | N/A |
| Sponsor | CMC Ambroise Paré |
| Enrollment | 27 |
| Study Type | INTERVENTIONAL |
| Conditions | Hallux Valgus and Bunion (Disorder); Morton Neuroma; Metatarsal Fracture; Ingrown Nail; Foot Wound |
| Interventions |
Foot surgery is a painful surgery that is usually scheduled in outpatients. A good management of analgesia is the crucial point. Regional anesthesia (RA) is the gold standard, that provides good anesthesia and a long duration of analgesia. The sciatic nerve block (or its branches) is the most adapted analgesic technique.
Limitation of proximal sciatic block is the motor block of the ankle and …
NCT03780452 — Compression Nail for Tibiocalcaneal Arthrodesis
| Status | Completed |
| Phase | N/A |
| Sponsor | University of Alabama at Birmingham |
| Enrollment | 13 |
| Study Type | OBSERVATIONAL |
| Conditions | Subtalar Arthritis; Ankle Arthritis |
| Interventions |
The purpose of this study is to determine the clinical efficacy of a novel dynamic compression intramedullary nail for tibiotalocalcaneal (TTC) arthrodesis
NCT04535999 — Open Label Study of the Effects of Secukinumab on Nail Psoriasis and Non-Invasive Measures of Enthesitis (Phase IV)
| Status | Completed |
| Phase | Phase 4 |
| Sponsor | University of Pennsylvania |
| Enrollment | 16 |
| Study Type | INTERVENTIONAL |
| Conditions | Psoriasis |
| Interventions |
This study will be an open label study of secukinumab for the treatment of nail psoriasis. Secukinumab is an FDA-approved treatment for psoriasis. We will examine time to response and different methods of defining nail disease response.
NCT05202366 — An Open-label Study Evaluating the Effectiveness of CGB-400 Topical Gel for Fungal Infection
| Status | Completed |
| Phase | N/A |
| Sponsor | CAGE Bio Inc. |
| Enrollment | 15 |
| Study Type | OBSERVATIONAL |
| Conditions | Fungal Infection; Onychomycosis; Tinea Unguium |
| Interventions |
The goal of the current study is to evaluate the ability of CGB-400, a proprietary eutectic mixture of GRAS compounds, to clear the toenail fungal growth and improve the appearance of the fungus affected area(s).
This is an open-label, single group POC study evaluating the effectiveness of CGB-400 Topical Gel for toenail fungal growth clearing. The study consists of a 12-week period with 5 cli…
NCT05435638 — Study Designed to Evaluate Safety and Efficacy of 1% Topical Formulation of KM-001 on Type 1 Punctate Palmoplantar Keratoderma or Pachyonychia Congenita Diseases
| Status | Completed |
| Phase | Phase 1 |
| Sponsor | Orvida Pharma (formerly Kamari Pharma) |
| Enrollment | 14 |
| Study Type | INTERVENTIONAL |
| Conditions | Punctate Palmoplantar Keratoderma Type 1; Pachyonychia Congenita |
| Interventions | ; ; |
In this phase 1 open label study for patients with type I punctate palmoplantar keratoderma or pachyonychia congenital, 2 arms will be recruited to be treated twice daily, with 1% topical KM-001.
Arm 1: up to 10 eligible patients will be treated for 12 weeks. Arm 2: up to 8 eligible patients will be treated for 16 weeks.
Treatment safety and efficacy will be assessed in the clinic visits (for…
NCT05956314 — Assessment of KM-001 - Safety, Tolerability, and Efficacy in Patients With PPPK1 or PC
| Status | Completed |
| Phase | Phase 1 |
| Sponsor | Orvida Pharma (formerly Kamari Pharma) |
| Enrollment | 18 |
| Study Type | INTERVENTIONAL |
| Conditions | Punctate Palmoplantar Keratoderma Type 1; Pachyonychia Congenita |
| Interventions | ; ; |
This Phase 1b, open-label, single-center, prospective trial will be assessing the safety, tolerability, and efficacy of topical KM-001 1% in patients with PPPK1 or PC diseases. In this study 2 cohorts will be recruited:
- Cohort 1: up to 11 eligible patients, will be enrolled to be treated twice daily, for 12 weeks, with 1% topical KM-001, on the plantar surfaces (2 feet).
- Cohort 2: up to …
NCT05674747 — Pilot Study of Swift Microwave Device for Onychomycosis
| Status | Completed |
| Phase | Phase 1 / Phase 2 |
| Sponsor | Mediprobe Research Inc. |
| Enrollment | 39 |
| Study Type | INTERVENTIONAL |
| Conditions | Onychomycosis of Toenail |
| Interventions | ; ; |
This is an open, single site, pilot study in Canadian subjects diagnosed with mild to moderate toenail onychomycosis caused by dermatophytes. Three microwave treatment frequencies will be compared for efficacy and safety, evaluated by frequency of treatment-related adverse events, clinical improvement of a treated target toenail and inactivation/elimination of fungus in the target toenail. Outc…
NCT06135298 — FARE Augmentation of Proximal Femoral Fractures With CaS/HA and Systemic ZA
| Status | Completed |
| Phase | Phase 4 |
| Sponsor | Aksaray University |
| Enrollment | 20 |
| Study Type | INTERVENTIONAL |
| Conditions | Trochanteric Fracture of Femur; Osteoporotic Fracture of Femur; Hip Fractures; Bone Density, Low |
| Interventions | ; ; |
The goal of this clinical trial is to investigate the new bone formation around a metal device in the femoral head in patients with osteoporotic hip fractures undergoing surgical treatment with nails. These surgeries have a high risk of fixation failure in patients with osteoporosis due to low bone quality. The main question we aim to answer are whether promoting new bone formation around the i…
NCT06274775 — Effect of an Educational Nail Biopsy Video on Pre-operative Anxiety, Health Literacy, and Patient Satisfaction
| Status | Completed |
| Phase | N/A |
| Sponsor | Weill Medical College of Cornell University |
| Enrollment | 30 |
| Study Type | INTERVENTIONAL |
| Conditions | Anxiety; Literacy; Satisfaction, Patient |
| Interventions |
The investigators are interested in studying the effect of an animated video depicting a nail biopsy procedure on the anxiety, health literacy, and satisfaction of participants recommended to undergo a nail biopsy procedure. The investigators hypothesize that the animated video will reduce preoperative anxiety, increase health literacy, and increase patient satisfaction in relation to nail biop…
NCT07041047 — Evaluation of Apaisant Serum - Ingrown Nails for Ingrown Toenails
| Status | Completed |
| Phase | N/A |
| Sponsor | Swiss Footcare Laboratories - Poderm Professional |
| Enrollment | 22 |
| Study Type | INTERVENTIONAL |
| Conditions | Ingrown Toenails; Ingrown Nail Inflammation |
| Interventions |
To open-label clinical study aims to evaluate the efficacy and safety of APAISANT SERUM - INGROWN NAILS, a Class IIa CE-marked medical device, in relieving pain and discomfort associated with inflamed ingrown nails. The study includes 22 subjects with ingrown nails at stage 1 or 2, who will apply the product twice daily for 7 days. The primary objective is to assess the reduction of pain using …
NCT06418750 — Evaluation of a Range of Dermo-cosmetic Products to Treat Skin and Nail Toxicity Linked to Bispecific Anti-GPRC5D Bispecific Antibodies in Multiple Myeloma Patients". Myeloma". Descriptive Pilot Study
| Status | Completed |
| Phase | N/A |
| Sponsor | Nantes University Hospital |
| Enrollment | 20 |
| Study Type | INTERVENTIONAL |
| Conditions | Myeloma Multiple |
| Interventions |
The aim of this study is to assess the efficacy of range of dermo-cosmetic products (hand/feet serum, nail strengthening solution nail strengthening solution, dissolving oil and gloves/slippers) based on natural products and designed for cancer patients)on bispecific Ac-induced skin and nail toxicity in MM patients treated with anti-CD3xGPRC5D bispecific antibodies.
The effects of supportive c…
NCT05612139 — Post-market Observational Study on JTIN Telescopic Nail in Osteogenesis Imperfecta Pediatric Patients
| Status | Completed |
| Phase | N/A |
| Sponsor | Orthofix s.r.l. |
| Enrollment | 14 |
| Study Type | OBSERVATIONAL |
| Conditions | Osteogenesis Imperfecta |
| Interventions |
This study has been planned as part of the Orthofix Srl post-market active surveillance plan for the collection of data on both the clinical performance and the safety profile of the JTIN.
The rationale of the proposed study is to update and support the pre-market clinical evaluation of the JTIN with Real World Evidence clinical data in a real-life surgical setting, in order to confirm the ben…
NCT06175013 — Evaluation of a Combination of Two Medical Devices and One Device Use in the Treatment of Toenail Onychomycosis
| Status | Completed |
| Phase | N/A |
| Sponsor | Swiss Footcare Laboratories - Poderm Professional |
| Enrollment | 44 |
| Study Type | INTERVENTIONAL |
| Conditions | Onychomycosis |
| Interventions | ; |
The goal of this clinical investigation is to evaluate the efficacy of the tested products in medium to moderate onychomycosis after 112 days of treatments.
The main question it aims to answer is the effectiveness of the use of a combination of two investigational devices (Sérum PURIFIANT + Sérum BOOSTER) on the percentage of healthy nail surface after 112 days of treatment.
Participants will…
Other (Withdrawn)
NCT04099979 — A Pilot Study to Explore the Role of Gut Flora in Psoriasis
| Status | Withdrawn |
| Phase | N/A |
| Sponsor | ProgenaBiome |
| Enrollment | N/A |
| Study Type | OBSERVATIONAL |
| Conditions | Psoriasis; Psoriasis Vulgaris; Psoriasis Universalis; Psoriasis Face; Psoriasis Nail |
| Interventions |
This study seeks to correlate microbiome sequencing data with information provided by patients and their medical records regarding Psoriasis.
Other (Terminated)
NCT06412939 — Retrospective Study on Clinical Performance and Safety Profile of Agile Nail
| Status | Terminated |
| Phase | N/A |
| Sponsor | Orthofix s.r.l. |
| Enrollment | 20 |
| Study Type | OBSERVATIONAL |
| Conditions | Fractures, Bone; Impending Fracture; Deformity; Bone |
| Interventions |
This study aims to retrospectively collect data from routine clinical practice in order to evaluate the safety profile of the Agile intramedullary nail, used in pediatric patients according to the manufacturer Instructions For Use (IFU) in the time frame from the time of surgery until the last follow-up visit available at the hospitals.