Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT04927702 · ClinicalTrials.gov registry record · NA

Assessment of Wound Closure Comparing Synthetic Hybrid-Scale Fiber Matrix With Standard of Care in Treating Diabetic Foot Ulcers (DFU) and With Living Cellular Skin Substitute in Treating Venous Leg Ulcers (VLU)

A NA study, sponsored by Acera Surgical.

Terminated
Registry status
NA
Development phase
48
Enrollment target

NCT04927702: Clinical Trial NA study, sponsored by Acera Surgical.

NCT04927702 is a NA study that was terminated before completion, run by Acera Surgical. The registered enrollment target is 48 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (97% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT04927702, a NA study, was terminated before completion, sponsored by Acera Surgical.

TERMINATED
Registry status
NA
Development phase
48 participants
Enrollment target

Study Summary

In participants with diabetic foot ulcers (DFUs), this study will assess complete wound closure by comparing synthetic hybrid-scale fiber matrix (Restrata®) with standard of care. In participants with venous leg ulcers (VLUs), this study will assess complete wound closure by comparing synthetic hybrid-scale fiber matrix (Restrata®) with living cellular skin substitute (Apligraf®)

Primary Outcome

The number of wounds in each treatment arm that achieved 100 percent epithelialization of wound as assessed by a blinded evaluator via review of a three-dimensional high resolution photo of the wound plus confirmation of no drainage or need for additional dressing 2 weeks after 100 percent epithelialization

Interventions

  • DEVICE Standard of Care
  • DEVICE Synthetic Hybrid-Scale Fiber Matrix
  • DEVICE Living Cellular Skin Substitute

Trial Details

FieldValue
Enrollment Target 48 participants
Start Date 2021-07-19
Est. Completion 2024-08-01
Phase NA
Acera Surgical

5 total trials

Why NCT04927702 stopped before completion

NCT04927702 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 48 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (97% lower).

The record links to 0 conditions, and to 3 interventions - of which Standard of Care is the first listed.

NCT04927702 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT04927702 about?

NCT04927702 is a clinical study titled "Assessment of Wound Closure Comparing Synthetic Hybrid-Scale Fiber Matrix With Standard of Care in Treating Diabetic Foot Ulcers (DFU) and With Living Cellular Skin Substitute in Treating Venous Leg Ulcers (VLU)". In participants with diabetic foot ulcers (DFUs), this study will assess complete wound closure by comparing synthetic hybrid-scale fiber matrix (Restrata®) with standard of care. In participants with venous leg ulcers (VLUs), this study will assess complete wound closure by comparing synthetic hyb...

What is the current status of trial NCT04927702?

This trial is currently terminated. It is a NA study. The enrollment target is 48 participants. The study started on 2021-07-19. Estimated completion is 2024-08-01.

What interventions are being tested in trial NCT04927702?

The interventions under investigation include: Standard of Care (DEVICE), Synthetic Hybrid-Scale Fiber Matrix (DEVICE), Living Cellular Skin Substitute (DEVICE).

Who is sponsoring clinical trial NCT04927702?

This trial is sponsored by Acera Surgical, which has 5 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT04927702's enrollment target sits among peer trials

48 1381st of 2000 higher than 601 of 2,000 other NA trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar enrollment target

  • NCT01765777 · 48 participants · NA

    Efficacy of Osteopathic Manipulative Medicine (OMM) and Phototherapy for Patients With Chronic Lower Back Pain

  • NCT03073343 · 48 participants · NA

    A Prospective, Randomized, Open Label Trial of Two Doses of Oral Betaine

  • NCT03431064 · 48 participants

    Lung Recruitment Maneuver as a Potential Predictor of Fluid Responsiveness in Mechanically Ventilated Pediatric Patients

  • NCT03514602 · 48 participants · NA

    Maternal Smoking Cessation and Pediatric Obesity Prevention

Similar registry start date

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

  • NCT07125183 · started 2026-12 · Phase 2

    Study on Efficacy and Tolerability of Weekly Doxorubicin in Elderly Patients With Advanced or Metastatic Leiomyosarcoma

  • NCT07292298 · started 2026-11 · Phase 2

    Phase 2 Single-Arm Rectal Cancer Brachytherapy for Patients With Low-Lying Residual Adenocarcinoma After Total Neoadjuvant Therapy to Improve Organ Preservation Rates

  • NCT04263285 · started 2026-10 · NA

    Treatment of Depression Post-SCI

Source: ClinicalTrials.gov NCT04927702, the US trial registry maintained by the National Library of Medicine. NCT04927702 (small enrollment · none site footprint · terminated) retrieved and formatted by PlainTrial, see methodology.