Clinical Trials for Nail Diseases

Currently registered clinical trials for Nail Diseases from ClinicalTrials.gov. 13 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 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.

StatusRecruiting
PhasePhase 3
SponsorSt. Louis University
Enrollment60
Study TypeINTERVENTIONAL
ConditionsBone 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

StatusRecruiting
PhasePhase 3
SponsorMajor Extremity Trauma Research Consortium
Enrollment1000
Study TypeINTERVENTIONAL
ConditionsTibial 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

StatusRecruiting
PhaseN/A
SponsorHerlev and Gentofte Hospital
Enrollment1000
Study TypeOBSERVATIONAL
ConditionsPsoriasis; 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

StatusRecruiting
PhaseN/A
SponsorHelse Stavanger HF
Enrollment170
Study TypeINTERVENTIONAL
ConditionsHip 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

StatusRecruiting
PhasePhase 2
SponsorHoth Therapeutics, Inc.
Enrollment152
Study TypeINTERVENTIONAL
ConditionsAcneiform 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

StatusRecruiting
PhaseN/A
SponsorOrthofix s.r.l.
Enrollment45
Study TypeOBSERVATIONAL
ConditionsLeg 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

StatusRecruiting
PhasePhase 2
SponsorAmtixBio Co., Ltd.
Enrollment120
Study TypeINTERVENTIONAL
ConditionsOnychomycosis
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

StatusRecruiting
PhasePhase 1
SponsorZagazig University
Enrollment36
Study TypeINTERVENTIONAL
ConditionsOnychomycosis
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

StatusRecruiting
PhasePhase 3
SponsorQueen Mary Hospital, Hong Kong
Enrollment40
Study TypeINTERVENTIONAL
ConditionsParonychia; 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

StatusRecruiting
PhaseN/A
SponsorOystershell NV
Enrollment88
Study TypeINTERVENTIONAL
ConditionsOnychomycosis
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

StatusRecruiting
PhaseN/A
SponsorCentre Hospitalier Universitaire de Nice
Enrollment10
Study TypeOBSERVATIONAL
ConditionsMelanoma
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.

StatusRecruiting
PhaseN/A
SponsorPakistan Institute of Medical Sciences
Enrollment312
Study TypeINTERVENTIONAL
ConditionsIngrown 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

StatusRecruiting
PhasePhase 3
SponsorWooshin Labottach Co., Ltd.
Enrollment72
Study TypeINTERVENTIONAL
ConditionsNail 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

StatusActive, not recruiting
PhaseN/A
SponsorMemorial Sloan Kettering Cancer Center
Enrollment546
Study TypeOBSERVATIONAL
ConditionsNon-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

StatusActive, not recruiting
PhaseN/A
SponsorSage Bionetworks
Enrollment1000
Study TypeOBSERVATIONAL
ConditionsPsoriatic 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

StatusActive, not recruiting
PhasePhase 2
SponsorTranslational Sciences, Inc.
Enrollment64
Study TypeINTERVENTIONAL
ConditionsPulmonary Embolism
Interventions;

Phase II trial of TS23

NCT05938361 — Efficacy of Tildrakizumab in Difficult-to-treat Areas in Psoriasis

StatusActive, not recruiting
PhaseN/A
SponsorClin4all
Enrollment120
Study TypeOBSERVATIONAL
ConditionsPsoriasis 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

StatusActive, not recruiting
PhaseN/A
SponsorChildren’s Hospital of Fudan University
Enrollment200
Study TypeINTERVENTIONAL
ConditionsMindfulness 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

StatusActive, not recruiting
PhaseN/A
SponsorChulalongkorn University
Enrollment50
Study TypeINTERVENTIONAL
ConditionsOnychomycosis 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

StatusActive, not recruiting
PhasePhase 2
SponsorVanda Pharmaceuticals
Enrollment50
Study TypeINTERVENTIONAL
ConditionsOnychomycosis 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

StatusActive, not recruiting
PhaseN/A
SponsorGlyconics Ltd
Enrollment100
Study TypeINTERVENTIONAL
ConditionsDiabetes 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

StatusNot yet recruiting
PhaseN/A
SponsorAssiut University
Enrollment50
Study TypeOBSERVATIONAL
ConditionsVitiligo; 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

StatusNot yet recruiting
PhaseN/A
SponsorShanghai Yueyang Integrated Medicine Hospital
Enrollment310
Study TypeOBSERVATIONAL
ConditionsPsoriasis (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)

StatusNot yet recruiting
PhaseN/A
SponsorChongqing Genrix Biopharmaceutical Co., Ltd
Enrollment1000
Study TypeOBSERVATIONAL
ConditionsPlaque 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,

StatusNot yet recruiting
PhaseN/A
SponsorKutahya City Hospital
Enrollment108
Study TypeINTERVENTIONAL
ConditionsIngrown 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

StatusNot yet recruiting
PhaseN/A
SponsorAssiut University
Enrollment3
Study TypeINTERVENTIONAL
ConditionsOsteopenia, 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

StatusNot yet recruiting
PhaseN/A
SponsorUniversity of Bologna
Enrollment80
Study TypeOBSERVATIONAL
ConditionsOnychomycosis 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

StatusNot yet recruiting
PhaseN/A
SponsorAssiut University
Enrollment40
Study TypeINTERVENTIONAL
ConditionsOnychomycosis
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

StatusNot yet recruiting
PhaseN/A
SponsorUniversity of Seville
Enrollment175
Study TypeINTERVENTIONAL
ConditionsIngrown 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

StatusNot yet recruiting
PhaseN/A
SponsorICIM International S.r.l.
Enrollment21
Study TypeINTERVENTIONAL
ConditionsNail 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

StatusNot yet recruiting
PhasePhase 1 / Phase 2
SponsorNorthwestern University
Enrollment44
Study TypeINTERVENTIONAL
ConditionsEpidermolytic 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

StatusEnrolling by invitation
PhaseN/A
SponsorMayo Clinic
Enrollment75
Study TypeINTERVENTIONAL
ConditionsGastric 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

StatusCompleted
PhaseN/A
SponsorUniversity Hospitals Cleveland Medical Center
Enrollment50
Study TypeOBSERVATIONAL
ConditionsOnychomycosis; 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

StatusCompleted
PhaseN/A
SponsorCentre Hospitalier Departemental Vendee
Enrollment319
Study TypeINTERVENTIONAL
ConditionsBreast 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

StatusCompleted
PhaseN/A
SponsorChulalongkorn University
Enrollment27
Study TypeINTERVENTIONAL
ConditionsOnychomycosis 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

StatusCompleted
PhaseN/A
SponsorCMC Ambroise Paré
Enrollment27
Study TypeINTERVENTIONAL
ConditionsHallux 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

StatusCompleted
PhaseN/A
SponsorUniversity of Alabama at Birmingham
Enrollment13
Study TypeOBSERVATIONAL
ConditionsSubtalar 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)

StatusCompleted
PhasePhase 4
SponsorUniversity of Pennsylvania
Enrollment16
Study TypeINTERVENTIONAL
ConditionsPsoriasis
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

StatusCompleted
PhaseN/A
SponsorCAGE Bio Inc.
Enrollment15
Study TypeOBSERVATIONAL
ConditionsFungal 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

StatusCompleted
PhasePhase 1
SponsorOrvida Pharma (formerly Kamari Pharma)
Enrollment14
Study TypeINTERVENTIONAL
ConditionsPunctate 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

StatusCompleted
PhasePhase 1
SponsorOrvida Pharma (formerly Kamari Pharma)
Enrollment18
Study TypeINTERVENTIONAL
ConditionsPunctate 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:

  1. 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).
  2. Cohort 2: up to …

NCT05674747 — Pilot Study of Swift Microwave Device for Onychomycosis

StatusCompleted
PhasePhase 1 / Phase 2
SponsorMediprobe Research Inc.
Enrollment39
Study TypeINTERVENTIONAL
ConditionsOnychomycosis 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

StatusCompleted
PhasePhase 4
SponsorAksaray University
Enrollment20
Study TypeINTERVENTIONAL
ConditionsTrochanteric 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

StatusCompleted
PhaseN/A
SponsorWeill Medical College of Cornell University
Enrollment30
Study TypeINTERVENTIONAL
ConditionsAnxiety; 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

StatusCompleted
PhaseN/A
SponsorSwiss Footcare Laboratories - Poderm Professional
Enrollment22
Study TypeINTERVENTIONAL
ConditionsIngrown 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

StatusCompleted
PhaseN/A
SponsorNantes University Hospital
Enrollment20
Study TypeINTERVENTIONAL
ConditionsMyeloma 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

StatusCompleted
PhaseN/A
SponsorOrthofix s.r.l.
Enrollment14
Study TypeOBSERVATIONAL
ConditionsOsteogenesis 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

StatusCompleted
PhaseN/A
SponsorSwiss Footcare Laboratories - Poderm Professional
Enrollment44
Study TypeINTERVENTIONAL
ConditionsOnychomycosis
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

StatusWithdrawn
PhaseN/A
SponsorProgenaBiome
EnrollmentN/A
Study TypeOBSERVATIONAL
ConditionsPsoriasis; 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

StatusTerminated
PhaseN/A
SponsorOrthofix s.r.l.
Enrollment20
Study TypeOBSERVATIONAL
ConditionsFractures, 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.