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NCT01143714 · ClinicalTrials.gov registry record · Phase 4

A Study to Look at the Effects of Four Weeks of Treatment on the Healing of Diabetic Foot Ulcers

A Phase 4 study of Diabetic Foot Ulcers, sponsored by Healthpoint.

Completed
Registry status
Phase 4
Development phase
57
Enrollment target
6
Study locations

NCT01143714 is a Phase 4 study of Diabetic Foot Ulcers that has completed, run by Healthpoint. The registered enrollment target is 57 participants, below the 230-participant average among 12 other Diabetic Foot Ulcers trials with a reported enrollment target (75% lower). The trial reports 6 study locations across 5 states.

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The verdict

NCT01143714, a Phase 4 study of Diabetic Foot Ulcers, has completed, sponsored by Healthpoint.

COMPLETED
Registry status
Phase 4
Development phase
57 participants
Enrollment target
6
Study locations

Study Summary

The purpose of this study is to assess the effect of four weeks of treatment with Santyl Ointment, compared to White Petrolatum, on the change from baseline in wound area of diabetic foot ulcers over four weeks, and on the proportion of subjects achieving complete wound closure within 12 weeks from initiation of treatment.

Conditions Studied

Interventions

  • DRUG Santyl
  • OTHER White Petrolatum

Study Locations (6)

Pennsylvania

  • The Foot and Ankle Institute of Western Pennsylvania - Pittsburgh
  • Center for Advanced Wound Care - Wyomissing

California

  • Olive View - UCLA Medical Center - Sylmar

Illinois

  • Northwestern University Feinberg School of Medicine - Chicago

Massachusetts

  • Boston Medical Center - Boston

Texas

  • Complete Family Foot Care - McAllen

Trial Details

FieldValue
Enrollment Target 57 participants
Start Date 2010-06
Est. Completion 2012-10
Phase Phase 4

Sponsor

Healthpoint

25 total trials

What the Registry Record Tells You About NCT01143714

The ClinicalTrials.gov registry entry for NCT01143714 describes a study currently listed as completed, categorized as Phase 4. The registered enrollment target is 57 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 230-participant average among 12 other Diabetic Foot Ulcers trials with a reported enrollment target (75% lower). The listed sponsor is Healthpoint, which has 25 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Diabetic Foot Ulcers appearing as the primary indexed condition, and to 2 interventions - of which Santyl is the first listed.

NCT01143714 reports 6 study locations spanning 5 distinct geographic areas - top geographies include Pennsylvania, California, Illinois.

Frequently Asked Questions

What is clinical trial NCT01143714 about?

NCT01143714 is a clinical study titled "A Study to Look at the Effects of Four Weeks of Treatment on the Healing of Diabetic Foot Ulcers". The purpose of this study is to assess the effect of four weeks of treatment with Santyl Ointment, compared to White Petrolatum, on the change from baseline in wound area of diabetic foot ulcers over four weeks, and on the proportion of subjects achieving complete wound closure within 12 weeks from ...

What is the current status of trial NCT01143714?

This trial is currently completed. It is a Phase 4 study. The enrollment target is 57 participants. The study started on 2010-06. Estimated completion is 2012-10.

What conditions does trial NCT01143714 study?

This clinical trial studies the following conditions: Diabetic Foot Ulcers.

What interventions are being tested in trial NCT01143714?

The interventions under investigation include: Santyl (DRUG), White Petrolatum (OTHER).

Who is sponsoring clinical trial NCT01143714?

This trial is sponsored by Healthpoint, which has 25 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT01143714 being conducted?

This trial has 6 study locations across California, Illinois, Massachusetts, Pennsylvania, Texas. 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

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.