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NCT04203745 · ClinicalTrials.gov registry record · NA

Nonablative Fractional Diode Laser for Treatment of Skin Resurfacing and Pigmented Lesions

A NA study, sponsored by Candela Corporation.

Completed
Registry status
NA
Development phase
26
Enrollment target

NCT04203745: Completed NA study, sponsored by Candela Corporation.

NCT04203745 is a NA study that has completed, run by Candela Corporation. The registered enrollment target is 26 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.

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The verdict

NCT04203745, a NA study, has completed, sponsored by Candela Corporation.

COMPLETED
Registry status
NA
Development phase
26 participants
Enrollment target

Study Summary

This study is intended to evaluate the efficacy and safety of a new diode fractional laser for skin resurfacing and treatment of pigmented lesions.

Primary Outcome

The primary efficacy endpoint was defined as improvement in the clearance of pigmented lesions, as assessed by three (3) blinded evaluators comparing photographs taken at Baseline/Pre-treatment and at the 1-month follow-up (post final treatment)

Interventions

  • DEVICE Nonablative Fractional Diode Laser

Trial Details

FieldValue
Enrollment Target 26 participants
Start Date 2019-09-18
Est. Completion 2021-08-05
Phase NA
Candela Corporation

12 total trials

What the finished NCT04203745 record still lists

NCT04203745 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 26 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 Nonablative Fractional Diode Laser is the first listed.

NCT04203745 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT04203745 about?

NCT04203745 is a clinical study titled "Nonablative Fractional Diode Laser for Treatment of Skin Resurfacing and Pigmented Lesions". This study is intended to evaluate the efficacy and safety of a new diode fractional laser for skin resurfacing and treatment of pigmented lesions.

What is the current status of trial NCT04203745?

This trial is currently completed. It is a NA study. The enrollment target is 26 participants. The study started on 2019-09-18. Estimated completion is 2021-08-05.

What interventions are being tested in trial NCT04203745?

The interventions under investigation include: Nonablative Fractional Diode Laser (DEVICE).

Who is sponsoring clinical trial NCT04203745?

This trial is sponsored by Candela Corporation, which has 12 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT04203745's enrollment target sits among peer trials

26 1710th of 2000 higher than 289 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

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Source: ClinicalTrials.gov NCT04203745, the US trial registry maintained by the National Library of Medicine. NCT04203745 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.