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

NCT01013792 · ClinicalTrials.gov registry record · NA

A Comparison of an Investigational Dressing to Tegaderm Matrix Wound Dressing in the Management of Diabetic Foot Ulcers

A NA study, sponsored by Solventum US.

Terminated
Registry status
NA
Development phase
30
Enrollment target

NCT01013792: Clinical Trial NA study, sponsored by Solventum US.

NCT01013792 is a NA study that was terminated before completion, run by Solventum US. The registered enrollment target is 30 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (98% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT01013792, a NA study, was terminated before completion, sponsored by Solventum US.

TERMINATED
Registry status
NA
Development phase
30 participants
Enrollment target

Study Summary

The primary objective is to: * Assess the effect of the Non-adherent study dressing to 3M Tegaderm Matrix Dressing with PHI technology on wound healing in patients with a diabetic foot ulcer. Secondary objectives are to: * Assess the adverse events that occur in subjects randomized to the investigational dressing in comparison to subjects randomized to the Tegaderm Matrix Dressing with PHI technology. * Assess the costs of using the investigational dressing compared to the Tegaderm Matrix Dressing with PHI technology. * Assess and compare the impact that these dressings have on patients' quality of life. * Assess the wound's biological response and pH to the study dressings.

Primary Outcome

A positive value indicates a reduction in area relative to baseline, while a negative value indicates an increase in area relative to baseline (at time of randomization), calculated as \[(Baseline - Week 8)/Baseline\] x 100%.

Interventions

  • DEVICE Wound Dressing

Trial Details

FieldValue
Enrollment Target 30 participants
Start Date 2009-11
Est. Completion 2012-07
Phase NA
Solventum US

41 total trials

Why NCT01013792 stopped before completion

NCT01013792 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 30 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (98% lower).

The record links to 0 conditions, and to 1 intervention - of which Wound Dressing is the first listed.

NCT01013792 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT01013792 about?

NCT01013792 is a clinical study titled "A Comparison of an Investigational Dressing to Tegaderm Matrix Wound Dressing in the Management of Diabetic Foot Ulcers". The primary objective is to: * Assess the effect of the Non-adherent study dressing to 3M Tegaderm Matrix Dressing with PHI technology on wound healing in patients with a diabetic foot ulcer. Secondary objectives are to: * Assess the adverse events that occur in subjects randomized to the investi...

What is the current status of trial NCT01013792?

This trial is currently terminated. It is a NA study. The enrollment target is 30 participants. The study started on 2009-11. Estimated completion is 2012-07.

What interventions are being tested in trial NCT01013792?

The interventions under investigation include: Wound Dressing (DEVICE).

Who is sponsoring clinical trial NCT01013792?

This trial is sponsored by Solventum US, which has 41 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT01013792's enrollment target sits among peer trials

30 1593rd of 2000 higher than 299 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

  • NCT00977977 · 30 participants · Phase 2

    Rituximab Plus Cyclosporine in Idiopathic Membranous Nephropathy

  • NCT01459107 · 30 participants · Phase 2

    Human Upper Extremity Allotransplantation

  • NCT01666080 · 30 participants · NA

    Second or Greater Allogeneic Hematopoietic Stem Cell Transplant Using Reduced Intensity Conditioning (RIC)

  • NCT01720836 · 30 participants · Phase 1

    Study of the Immune Response of MUC1 (Mucin1) Peptide Vaccine for Non-small Cell Lung Cancer

Similar registry start date

  • NCT05988463 · started 2027-01-01 · Phase 1

    Dose-Escalation Study of Artesunate Patients With IPF

  • NCT07219706 · started 2026-12-10 · NA

    Dietary Fiber and Time Restricted Eating

  • NCT02831335 · started 2026-12-01

    Technical Development of Multi-Parametric Renocerebral MRI

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

Source: ClinicalTrials.gov NCT01013792, the US trial registry maintained by the National Library of Medicine. NCT01013792 (small enrollment · none site footprint · terminated) retrieved and formatted by PlainTrial, see methodology.