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NCT07364630 · ClinicalTrials.gov registry record · Phase 4

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.

A Phase 4 study of Diabetic Foot Ulcer and Venous Leg Ulcer, sponsored by BioLab Holdings.

Recruiting
Registry status
Phase 4
Development phase
50
Enrollment target
1
Study location

NCT07364630 is a Phase 4 study of Diabetic Foot Ulcer and Venous Leg Ulcer that is actively recruiting participants, run by BioLab Holdings. The registered enrollment target is 50 participants, below the 254-participant average among 67 other Diabetic Foot Ulcer trials with a reported enrollment target (80% lower). The trial reports 1 study location across 1 state.

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The verdict

NCT07364630, a Phase 4 study of Diabetic Foot Ulcer and Venous Leg Ulcer, is actively recruiting participants, sponsored by BioLab Holdings.

RECRUITING
Registry status
Phase 4
Development phase
50 participants
Enrollment target
1
Study location

Study Summary

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.

Interventions

  • OTHER Tri-Membrane Wrap™ DFU
  • OTHER Membrane Wrap™ DFU
  • OTHER Membrane Wrap-Lite™ DFU
  • OTHER Membrane Wrap-Hydro™ DFU
  • OTHER Tri-Membrane Wrap™ VLU

Study Locations (1)

Pennsylvania

  • Center for Foot and Ankle Disorders - Philidelphia

Trial Details

FieldValue
Enrollment Target 50 participants
Start Date 2026-01-02
Est. Completion 2027-01
Phase Phase 4

Sponsor

BioLab Holdings

4 total trials

What the Registry Record Tells You About NCT07364630

The ClinicalTrials.gov registry entry for NCT07364630 describes a study currently listed as recruiting, categorized as Phase 4. The registered enrollment target is 50 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 254-participant average among 67 other Diabetic Foot Ulcer trials with a reported enrollment target (80% lower). The listed sponsor is BioLab Holdings, which has 4 total studies on file at ClinicalTrials.gov.

The record links to 9 conditions, with Diabetic Foot Ulcer appearing as the primary indexed condition, and to 5 interventions - of which Tri-Membrane Wrap™ DFU is the first listed.

NCT07364630 reports 1 study location spanning 1 distinct geographic area - top geographies include Pennsylvania.

Frequently Asked Questions

What is clinical trial NCT07364630 about?

NCT07364630 is a clinical study titled "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.

What is the current status of trial NCT07364630?

This trial is currently recruiting. It is a Phase 4 study. The enrollment target is 50 participants. The study started on 2026-01-02. Estimated completion is 2027-01.

What conditions does trial NCT07364630 study?

This clinical trial studies the following conditions: Diabetic Foot Ulcer, Venous Leg Ulcer, Ulcer, Venous Ulcer, Ulcer Foot.

What interventions are being tested in trial NCT07364630?

The interventions under investigation include: Tri-Membrane Wrap™ DFU (OTHER), Membrane Wrap™ DFU (OTHER), Membrane Wrap-Lite™ DFU (OTHER), Membrane Wrap-Hydro™ DFU (OTHER), Tri-Membrane Wrap™ VLU (OTHER).

Who is sponsoring clinical trial NCT07364630?

This trial is sponsored by BioLab Holdings, which has 4 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT07364630 being conducted?

This trial has 1 study location across Pennsylvania. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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

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