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

NCT01910831 · ClinicalTrials.gov registry record · Phase 4

Study to Assess DerMend Moisturizing Bruise Formula in Improving the Appearance of Chronically Aged Forearms and Hands

A Phase 4 study, sponsored by The Center for Clinical and Cosmetic Research.

Completed
Registry status
Phase 4
Development phase
20
Enrollment target

NCT01910831: Completed Phase 4 study, sponsored by The Center for Clinical and Cosmetic Research.

NCT01910831 is a Phase 4 study that has completed, run by The Center for Clinical and Cosmetic Research. The registered enrollment target is 20 participants, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (96% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT01910831, a Phase 4 study, has completed, sponsored by The Center for Clinical and Cosmetic Research.

COMPLETED
Registry status
Phase 4
Development phase
20 participants
Enrollment target

Study Summary

To determine the efficacy (measured at 12 weeks) of DerMend Moisturizing Bruise Formula in improving the appearance of bruising and reducing the appearance of photoaging of the forearms and hands in mature skin. Assessments will be made through ongoing objective measurements and clinical ratings. To confirm the safety (local tolerance) of DerMend Moisturizing Bruise Formula.

Primary Outcome

To determine the efficacy (measured at 12 weeks) of DerMend Moisturizing Bruise Formula in improving the appearance of bruising and reducing the appearance of photoaging of the forearms and hands in mature skin.

Interventions

  • DRUG DerMend Moisturizing Bruise Formula
  • DRUG Non-active placebo control

Trial Details

FieldValue
Enrollment Target 20 participants
Start Date 2013-07
Est. Completion 2014-01
Phase Phase 4

What the finished NCT01910831 record still lists

NCT01910831 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 20 participants, a relatively small participant target, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (96% lower).

The record links to 0 conditions, and to 2 interventions - of which DerMend Moisturizing Bruise Formula is the first listed.

NCT01910831 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT01910831 about?

NCT01910831 is a clinical study titled "Study to Assess DerMend Moisturizing Bruise Formula in Improving the Appearance of Chronically Aged Forearms and Hands". To determine the efficacy (measured at 12 weeks) of DerMend Moisturizing Bruise Formula in improving the appearance of bruising and reducing the appearance of photoaging of the forearms and hands in mature skin. Assessments will be made through ongoing objective measurements and clinical ratings. T...

What is the current status of trial NCT01910831?

This trial is currently completed. It is a Phase 4 study. The enrollment target is 20 participants. The study started on 2013-07. Estimated completion is 2014-01.

What interventions are being tested in trial NCT01910831?

The interventions under investigation include: DerMend Moisturizing Bruise Formula (DRUG), Non-active placebo control (DRUG).

Who is sponsoring clinical trial NCT01910831?

This trial is sponsored by The Center for Clinical and Cosmetic Research, which has 9 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT01910831's enrollment target sits among peer trials

20 1753rd of 2000 higher than 167 of 2,000 other Phase 4 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 4 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

  • NCT00573339 · 20 participants

    Cardiac Magnetic Resonance Imaging (MRI) Normal Reference Control Group Testing

  • NCT00692939 · 20 participants · Phase 1

    Autologous Stem Cell Transplantation for Crohn's Disease

  • NCT00967785 · 20 participants · Phase 1

    A Phase I Study of Mozobil in the Treatment of Patients With WHIMS

  • NCT01406691 · 20 participants · Phase 4

    Light Flashes to Treat Delayed Sleep Phase Disorder (DSPD)

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 NCT01910831, the US trial registry maintained by the National Library of Medicine. NCT01910831 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.