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NCT02032641 · ClinicalTrials.gov registry record · NA

Evaluation of Non-Ablative Laser for Treatment of Direct Brow Lift Scars

A NA study of Scar, sponsored by University of Miami.

Completed
Registry status
NA
Development phase
9
Enrollment target
2
Study locations

NCT02032641: Completed NA study of Scar, sponsored by University of Miami.

NCT02032641 is a NA study of Scar that has completed, run by University of Miami. The registered enrollment target is 9 participants, below the 48-participant average among 15 other Scar trials with a reported enrollment target (81% lower). The trial reports 2 study locations across 1 state. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT02032641, a NA study of Scar, has completed, sponsored by University of Miami.

COMPLETED
Registry status
NA
Development phase
9 participants
Enrollment target
2
Study locations

Study Summary

The purpose of this study is to determine the efficacy of the 1064nm Neodymium yttrium aluminum garnet (Nd:YAG) laser (Laser Genesis, Cutera TM) in the treatment of surgical scar after direct brow lift.

Primary Outcome

Which scar, overall, appears to have improved more from initial to final visit, as rated by blinded examiner of photographs

Conditions Studied

Interventions

  • DEVICE Laser treatment

Study Locations (2)

Florida

  • Bascom Palmer Eye Institute - Miami
  • Bascom Palmer Eye Institute - Plantation

Trial Details

FieldValue
Enrollment Target 9 participants
Start Date 2013-06
Est. Completion 2015-05
Phase NA
University of Miami

721 total trials

What the finished NCT02032641 record still lists

NCT02032641 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 9 participants, a relatively small participant target, below the 48-participant average among 15 other Scar trials with a reported enrollment target (81% lower).

The record links to 1 condition, with Scar appearing as the primary indexed condition, and to 1 intervention - of which Laser treatment is the first listed.

NCT02032641 reports a single indexed study location in Florida.

Frequently Asked Questions

What is clinical trial NCT02032641 about?

NCT02032641 is a clinical study titled "Evaluation of Non-Ablative Laser for Treatment of Direct Brow Lift Scars". The purpose of this study is to determine the efficacy of the 1064nm Neodymium yttrium aluminum garnet (Nd:YAG) laser (Laser Genesis, Cutera TM) in the treatment of surgical scar after direct brow lift.

What is the current status of trial NCT02032641?

This trial is currently completed. It is a NA study. The enrollment target is 9 participants. The study started on 2013-06. Estimated completion is 2015-05.

What conditions does trial NCT02032641 study?

This clinical trial studies the following conditions: Scar.

What interventions are being tested in trial NCT02032641?

The interventions under investigation include: Laser treatment (DEVICE).

Who is sponsoring clinical trial NCT02032641?

This trial is sponsored by University of Miami, which has 721 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT02032641 being conducted?

This trial has 2 study locations across Florida. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Similar trials for Scar

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

Where NCT02032641's enrollment target sits among peer trials

9 16th of 15 the lowest of 15 other Scar trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Scar 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

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Source: ClinicalTrials.gov NCT02032641, the US trial registry maintained by the National Library of Medicine. NCT02032641 (small enrollment · single site footprint · completed) retrieved and formatted by PlainTrial, see methodology.