Wound Care

7

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

Condition / disease
Location
Status: Recruiting

Registry of Outcomes of Dezawa MuseCells®

The goal of this observational study is to learn about the long-term effects of Dezawa MuseCells to treat various diseases. The Primary Goal: What is the short-term and long- term outcomes of Dezawa Musecells? Participants treated with Dezawa MuseCells as part of their regular medical care and will answer online survey questions about symptoms and clinical outcomes for 5 years.

Participants needed: 5,000
Trial details
Age: Up to 89Biological sex: AllType: ObservationalSponsor: MuseCell Innovations Pte LTDUpdated: Jun 12, 2026Locations: 2Duration: 5 Years
Eligibility criteria

Received Dezawa MuseCells® as Part of Routine Clinical Care [+7]

Not Receive Dezawa MuseCells®-Individuals who have not been treated with Dezawa... [+8]

Status: Not yet recruiting

AI-Based Wound Monitoring: Automated Wound Progression Assessment Via Marker-Free Image Sequence

This study aims to develop a low-cost, marker-free intelligent wound assessment system that can analyze wound photos taken with a standard smartphone. By comparing wound images over time, the system will generate a quantifiable Wound Progression Index (WPI) to provide objective feedback on whether a wound is improving, stable, or worsening. The long-term goal is to support early detection of wound deterioration and improve wound care in both clinical and home settings.

Participants needed: 1,000
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: National Taiwan University HospitalUpdated: Jun 2, 2026Locations: 1
Eligibility criteria

(1) Presence of a hard-to-heal wound that has remained unhealed for more than on...

Wounds whose margins could not be fully included within the imaging field.

Status: Not yet recruiting

Using WoundPilot to Support Wound Care Decisions in Patients With Chronic Wounds

This study evaluates whether a digital decision support tool, called WoundPilot, can help primary care nurses make more accurate and consistent decisions when caring for patients with chronic wounds. In daily practice, treatment decisions for chronic wounds can vary between clinicians, even when they assess the same patient. This variation may lead to delays in appropriate care, inconsistent treatment choices, or unnecessary referrals. WoundPilot was developed to guide clinicians through a structured wound assessment and link this assessment to clear treatment recommendations. In this study, primary care nurses will assess a series of clinical cases either with or without the support of WoundPilot. Their decisions will be compared with an expert reference standard to determine whether the use of WoundPilot improves the accuracy of decisions and reduces differences between nurses. The results of this study will help determine whether WoundPilot can support more consistent and evidence-based wound care in clinical practice.

Participants needed: 40
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: University GhentUpdated: May 1, 2026Locations: 1
Eligibility criteria

Primary care nurses involved in wound care decision-making [+4]

Nurses not involved in wound care decision-making [+3]

Status: Not yet recruiting

Plasma Therapy for Diverse Wounds

This study is a prospective, multicenter, real-world observational study. It aims to evaluate whether adding plasma device therapy to standard wound care is effective and safe for treating different types of wounds, including acute wounds (such as burns and surgical incisions), chronic wounds (such as diabetic foot ulcers and pressure injuries), post-grafting wounds, and sutured wounds. A total of 500 patients receiving standard wound care plus plasma therapy will be enrolled from multiple hospitals across China. Their outcomes will be compared with 500 matched patients who received standard wound care alone. The main outcomes include wound healing rate at 4 weeks, time to complete wound closure, pain relief, scar formation, and any side effects. Patients will be followed for up to 6 months.

Participants needed: 1,000
Trial details
Biological sex: AllType: ObservationalSponsor: First Affiliated Hospital, Sun Yat-Sen UniversityUpdated: Apr 28, 2026Duration: 6 Months
Eligibility criteria

Presence of any of the following wound types: acute wounds (burns, trauma, surgi... [+3]

Active malignant tumor involving the wound area. [+4]

Status: Recruiting

The Pain Reduction Using Immersive Virtual Reality During Wound Care Evaluation Study at Maimonides (PRISM) - Pilot Study

This study will test whether immersive virtual reality (iVR) can reduce pain and discomfort during wound care for residents living in long-term care (LTC). Pressure ulcers are common and painful among older adults, and dressing changes often cause additional distress. Up to 20 residents at the Donald Berman Maimonides Geriatric Centre will use virtual reality headsets during routine wound care. The headsets display calm, low-stimulus scenes (e.g., puppies in a meadow) designed to distract and comfort participants. Each participant will take part for six weeks in three phases: * Two weeks of usual wound care (baseline) * Two weeks using virtual reality during wound care (intervention) * Two weeks of usual care again (washout) Pain will be assessed using validated tools, and the research team will also observe agitation, mood, and other behavioral indicators. Nursing staff will provide feedback on feasibility and acceptability of iVR use in LTC settings.

Participants needed: 25
Trial details
Biological sex: AllType: InterventionalSponsor: McGill UniversityUpdated: Mar 5, 2026Locations: 2
Eligibility criteria

Resident of LTC for ≥2 weeks [+3]

Blindness, severe cataracts, or glaucoma [+4]

Status: Not yet recruiting

A PAC Post-Market Clinical Study to Demonstrate Color Change in the WoundCue™ Kit When an Elevated Inhibitory Bacterial and/or Fungal Load is Present in a Wound

The purpose of this research is to test if the investigational ParaNano WoundCue Kit can detect elevated inhibitory bacterial and/or fungal loads.

Participants needed: 50
Trial details
Age: 21+Biological sex: AllType: InterventionalSponsor: ParaNano, Inc.Updated: Jan 29, 2026
Eligibility criteria

Subject's target treatment area has a surface area larger than 5 cm2.

Status: Not yet recruiting

The Effect of Wound Care Education Using the Jigsaw IV Learning Technique on Nursing Students' Knowledge, Collaborative Learning, and Academic Motivation

This study aims to investigate the effects of wound care education given with the jigsaw IV learning technique on the knowledge, collaborative learning and motivation levels of nursing students. Second-year nursing students will be divided into two groups with simple randomization. The intervention group will be given a wound care training program with the jigsaw IV technique. The control group will be given wound care training with traditional education. Pre-test data will be collected before the training and post-test data will be collected after the training.

Participants needed: 100
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Agri Ibrahim Cecen UniversityUpdated: May 8, 2025
Eligibility criteria

Not having taken a wound care education before [+1]

Being a nurse who graduated from secondary school and working in the clinic, [+3]