Surgical Wound Dehiscence

3

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

Condition / disease
Location
Status: Recruiting

A Real-World Registry of Chronic Wounds and Ulcers

WOUNDJOURNEY is a longitudinal, real-world, observational registry designed to capture the full clinical course and patient journey associated with chronic wounds and ulcers. Data are collected during routine care from over 1,400 clinicians across the USA and Puerto Rico using a highly structured certified electronic health record (EHR) or electronic data capture (EDC) system. Data are transmitted daily to the U.S. Wound Registry (USWR), a CMS-recognized Qualified Clinical Data Registry (QCDR). The registry captures real-time, research-ready data on patient demographics, comorbidities, wound characteristics, standard-of-care treatments, complications, and advanced therapeutics. It supports robust, fit-for-purpose real-world evidence generation by enabling risk-adjusted outcome analysis, comparative effectiveness research, and quality improvement across diverse sites of care.

Participants needed: 300,000
Trial details
Biological sex: AllType: ObservationalSponsor: U.S. Wound RegistryUpdated: Jul 16, 2025Locations: 1Duration: 5 Years
Eligibility criteria

Presence of one or more chronic wounds or ulcers of any etiology [+5]

Status: Available

Dermacyte® Liquid for Treatment of Cutaneous Ulcers and Wounds

The objective of this study is to make Dermacyte Liquid available on an expanded access basis to treat cutaneous ulcers and wounds refractory to initial treatment or that do not have adequate alternative treatments. Minimal data will be collected to evaluate the efficacy and safety of Dermacyte Liquid.

Trial details
Age: 18+Biological sex: AllType: Expanded AccessSponsor: Merakris TherapeuticsUpdated: Feb 25, 2025Locations: 1
Eligibility criteria

Must be 18 years of age or older [+1]

Must not be pregnant or lactating [+2]

Status: Recruiting

Real World Evidence with the Debritom+ TM Novel Micro Water Jet Technology At a Single Wound Center

Prospective, single-blinded, single-center, parallel group, randomized controlled trial (RCT) to assess rate and frequency of wound healing and associated financial savings, when using Medaxis debritom+ versus standard of care as a choice of debridement method, where both arms follow normal wound care practice in use of advanced wound care treatments.

Participants needed: 180
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Medaxis, LLCUpdated: Nov 21, 2024Locations: 1
Eligibility criteria

At least 18 years old. [+10]

The index ulcer will be the largest ulcer if two or more VLUs are present and wi... [+28]