Venous Ulcer

9

Review clinical trials related to Venous Ulcer. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Not yet recruiting

The GORE® VIABAHN® FORTEGRA Venous Stent Post-Approval Study

This study is a prospective, multicenter, single-arm post-market clinical study to evaluate the GORE® VIABAHN® FORTEGRA Venous Stent in real-world use.

Participants needed: 150
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: W.L.Gore & AssociatesUpdated: May 14, 2026
Eligibility criteria

Presence of a lesion necessitating treatment with the GORE® VIABAHN® FORTEGRA Ve... [+8]

Patient is contraindicated for treatment with the GORE® VIABAHN® FORTEGRA Venous...

Status: Recruiting

The GORE® VIABAHN® FORTEGRA Venous Stent Iliofemoral Study

This study is a prospective, non-randomized, multicenter, single-arm, clinical study to evaluate the performance, safety and efficacy of the GORE® VIABAHN® FORTEGRA Venous Stent (formerly known as GORE® VIAFORT Vascular Stent) for treatment of symptomatic iliofemoral venous obstruction.

Participants needed: 165
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: W.L.Gore & AssociatesUpdated: Apr 9, 2026Locations: 27
Eligibility criteria

Patient is at least 18 years of age. [+8]

Patient has DVT in the target areas with symptom onset date greater than 14 days... [+30]

Status: Recruiting

Monitoring of Venous Ulcers Using a Bioimpedance Measurement Based Method and System

The purpose of this study is to investigate the functionality of a new type of wound monitoring method and measurement system for monitoring healing of venous ulcers. The system is consisted of a wound dressing with electrodes (eDressing), a bioimpedance measurement device and a mobile phone application.

Participants needed: 20
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: CutoSense OyUpdated: Mar 17, 2026Locations: 2
Eligibility criteria

Age at least 18 years [+7]

Clinical wound infection at the time of the study [+7]

Status: Recruiting

Tissue Repair Gel in Venous Leg Ulcers (US)

The goal of this clinical trial is to learn if TR987 0.1% gel + Standard of Care works better than Standard of Care alone to treat Venous Leg Ulcers (VLUs). It will also provide additional information about the safety of drug TR987 0.1% gel.

Participants needed: 312
Trial details
Phase: Phase 3Age: 18+Biological sex: AllType: InterventionalSponsor: TR TherapeuticsUpdated: Feb 12, 2026Locations: 33
Eligibility criteria

Adults 18 years and older [+7]

Target ulcer has been treated with prohibited medications or therapies. [+4]

Status: Recruiting

A Multicenter, Prospective, Controlled Modified Multi-Platform Trial Assessing the Efficacy of Human Placental Membrane Products and Standard of Care in the Management of Nonhealing Diabetic Foot Ulcers and Venous Leg Ulcers.

The study is a multicenter, prospective, controlled modified multi-platform trial assessing the efficacy of human placental membrane products and standard of care in the management of nonhealing diabetic foot ulcers and venous leg ulcers.

Participants needed: 50
Trial details
Phase: Phase 4Age: 18+Biological sex: AllType: InterventionalSponsor: BioLab HoldingsUpdated: Feb 9, 2026Locations: 1
Eligibility criteria

The potential subject must be at least 18 years of age or older. [+6]

The potential subject is known to have a life expectancy of < 6 months. [+19]

Status: Recruiting

Fetal Cell Receptors Repertoire

The purpose of this study is to describe the transcriptomic profile of foetal cells in post-partum and more specifically to determine which chemokine receptors are overexpressed in foetal cells in post-partum women with wounds To do so, the investigators will isolate foetal cells from the peripheral blood of healthy controls post partum women as well as from post partum women with skin ulcers and then perform RNA sequencing.

Participants needed: 160
Trial details
Biological sex: AllType: InterventionalSponsor: Assistance Publique - Hôpitaux de ParisUpdated: Sep 12, 2025Locations: 1
Eligibility criteria

Adult women, [+7]

Minors (for patients) [+4]

Status: Recruiting

Tissue Repair Gel in Venous Leg Ulcers in AU/US

The goal of this clinical trial is to learn if TR987 0.1% gel + Standard of Care works better than Standard of Care alone to treat Venous Leg Ulcers (VLUs). It will also provide additional information about the safety of drug TR987 0.1% gel.

Participants needed: 312
Trial details
Phase: Phase 3Age: 18+Biological sex: AllType: InterventionalSponsor: TR TherapeuticsUpdated: Apr 2, 2025Locations: 12
Eligibility criteria

Adults 18 years and older [+7]

Target ulcer has been treated with prohibited medications or therapies. [+5]

Status: Recruiting

Evaluating the Durability of Closure for Venous Leg Ulcers

The goal of this observational study is to determine the durability of closure for venous leg ulcer subjects that achieved closure in the THOR trial.

Participants needed: 150
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Kerecis Ltd.Updated: Jan 24, 2025Locations: 1
Eligibility criteria

1. Subjects must have participated in the THOR trial and achieved complete closu...

1. Subjects who did not participate in the THOR trial. 2. Subjects who participa...

Status: Not yet recruiting

Shock Wave Versus Low Level Laser on Chronic Venous Ulcer

To find out the difference in the effect of shock wave therapy and low level laser therapy on venous ulcer patient As regards the following outcomes; 1. medical state of patient no ( diabetes, hypertension,obesity,cancer , rheumatoid) 2. The degree of ulcer 3. recurrence of ulcer 4. The degree of pain and disabilities 5. inflammatory marker

Participants needed: 45
Trial details
Age: 45-60Biological sex: AllType: InterventionalSponsor: Beni-Suef UniversityUpdated: Jan 3, 2025
Eligibility criteria

All old age patients will be [+5]

-Diabetes [+10]