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ACTIVE NOT RECRUITING

A REAL WORLD DATA COLLECTION OF HUMAN AMNIOTIC MEMBRANE(S) ON DIABETIC FOOT ULCERS, VENOUS LEG ULCERS, PRESSURE ULCERS AND POST OPERATIVE WOUNDS

NCT07078968 · View on ClinicalTrials.gov ↗

Study Summary

This study is designed to evaluate the effectiveness of Tri-Membrane Wrap™, Membrane Wrap™ and Membrane Wrap-Hydro™ compared to the effectiveness of Standard of Care alone though a retrospective data collection.

Interventions

  • OTHER Standard of Care
  • DEVICE Membrane Wrap™
  • DEVICE Tri-Membrane Wrap™
  • DEVICE Membrane Wrap-Hydro™

Study Locations (4)

Texas

  • Houston Foot and Ankle Care — Houston
  • Houston Foot Dr — Houston

Arizona

  • Athena Specialty Group — Phoenix

New Jersey

  • Revive Advanced Wound Care — Toms River

Trial Details

FieldValue
Enrollment Target 500 participants
Start Date 2025-04-23
Est. Completion 2025-10

Sponsor

BioLab Holdings

32 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT07078968

The ClinicalTrials.gov registry entry for NCT07078968 describes a study currently listed as active not recruiting. It is categorized as an unspecified phase, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 500 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is BioLab Holdings, which has 32 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 3 conditions, with Diabetic Foot Ulcer (DFU) appearing as the primary indexed condition, and to 4 interventions — of which Standard of Care is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT07078968 reports 4 study locations spanning 3 distinct geographic areas — top geographies include Texas, Arizona, New Jersey. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT07078968 about?

NCT07078968 is a clinical study titled "A REAL WORLD DATA COLLECTION OF HUMAN AMNIOTIC MEMBRANE(S) ON DIABETIC FOOT ULCERS, VENOUS LEG ULCERS, PRESSURE ULCERS AND POST OPERATIVE WOUNDS". This study is designed to evaluate the effectiveness of Tri-Membrane Wrap™, Membrane Wrap™ and Membrane Wrap-Hydro™ compared to the effectiveness of Standard of Care alone though a retrospective data collection.

What is the current status of trial NCT07078968?

This trial is currently active not recruiting. The enrollment target is 500 participants. The study started on 2025-04-23. Estimated completion is 2025-10.

What conditions does trial NCT07078968 study?

This clinical trial studies the following conditions: Diabetic Foot Ulcer (DFU), Venous Leg Ulcer (VLU), Pressure Ulcer (PU). These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT07078968?

The interventions under investigation include: Standard of Care (OTHER), Membrane Wrap™ (DEVICE), Tri-Membrane Wrap™ (DEVICE), Membrane Wrap-Hydro™ (DEVICE). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT07078968?

This trial is sponsored by BioLab Holdings, which has 32 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT07078968 being conducted?

This trial has 4 study locations across Arizona, New Jersey, Texas. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial