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

NCT06629506 · ClinicalTrials.gov registry record · NA

MicroMatrix® Flex in Tunneling Wounds

A NA study, sponsored by Integra LifeSciences Corporation.

Completed
Registry status
NA
Development phase
25
Enrollment target

NCT06629506 is a NA study that has completed, run by Integra LifeSciences Corporation. The registered enrollment target is 25 participants.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT06629506, a NA study, has completed, sponsored by Integra LifeSciences Corporation.

COMPLETED
Registry status
NA
Development phase
25 participants
Enrollment target

Study Summary

To evaluate the safety and performance of MicroMatrix® Flex in subjects with wounds complicated by tunneling and/or undermining features.

Interventions

  • DEVICE MicroMatrix® Flex
  • DEVICE MicroMatrix® UBM Particulate
  • DEVICE Cytal® Wound Matrix 2-Layer

Trial Details

FieldValue
Enrollment Target 25 participants
Start Date 2024-12-12
Est. Completion 2025-08-31
Phase NA

Sponsor

Integra LifeSciences Corporation

60 total trials

What the Registry Record Tells You About NCT06629506

The ClinicalTrials.gov registry entry for NCT06629506 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 25 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Integra LifeSciences Corporation, which has 60 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 3 interventions - of which MicroMatrix® Flex is the first listed.

NCT06629506 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT06629506 about?

NCT06629506 is a clinical study titled "MicroMatrix® Flex in Tunneling Wounds". To evaluate the safety and performance of MicroMatrix® Flex in subjects with wounds complicated by tunneling and/or undermining features.

What is the current status of trial NCT06629506?

This trial is currently completed. It is a NA study. The enrollment target is 25 participants. The study started on 2024-12-12. Estimated completion is 2025-08-31.

What interventions are being tested in trial NCT06629506?

The interventions under investigation include: MicroMatrix® Flex (DEVICE), MicroMatrix® UBM Particulate (DEVICE), Cytal® Wound Matrix 2-Layer (DEVICE).

Who is sponsoring clinical trial NCT06629506?

This trial is sponsored by Integra LifeSciences Corporation, which has 60 total clinical trials registered on ClinicalTrials.gov.

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

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.