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

NCT06469398 · ClinicalTrials.gov registry record · NA

A Post Market Device Study for the Treatment of Acne

A NA study of Acne Vulgaris, sponsored by Cutera.

Active
Registry status
NA
Development phase
50
Enrollment target
3
Study locations

NCT06469398: Active NA study of Acne Vulgaris, sponsored by Cutera.

NCT06469398 is a NA study of Acne Vulgaris that is active but no longer recruiting, run by Cutera. The registered enrollment target is 50 participants, below the 275-participant average among 67 other Acne Vulgaris trials with a reported enrollment target (82% lower). The trial reports 3 study locations across 3 states. According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT06469398, a NA study of Acne Vulgaris, is active but no longer recruiting, sponsored by Cutera.

ACTIVE NOT RECRUITING
Registry status
NA
Development phase
50 participants
Enrollment target
3
Study locations

Study Summary

To evaluate the safety and efficacy of the Cutera laser system for the treatment of acne vulgaris.

Conditions Studied

Interventions

  • DEVICE Cutera Laser System

Study Locations (3)

Florida

  • Dermatology of Boca - Boca Raton

New Jersey

  • Schweiger Dermatology PC, Reseach Division - Hackensack

Texas

  • Bellaire Dermatology Associates - Bellaire

Trial Details

FieldValue
Enrollment Target 50 participants
Start Date 2022-07-21
Est. Completion 2025-08-18
Phase NA
Cutera

37 total trials

What the registry record for NCT06469398 still lists

NCT06469398 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 50 participants, a relatively small participant target, below the 275-participant average among 67 other Acne Vulgaris trials with a reported enrollment target (82% lower).

The record links to 1 condition, with Acne Vulgaris appearing as the primary indexed condition, and to 1 intervention - of which Cutera Laser System is the first listed.

NCT06469398 reports a single indexed study location in Florida, New Jersey, Texas.

Frequently Asked Questions

What is clinical trial NCT06469398 about?

NCT06469398 is a clinical study titled "A Post Market Device Study for the Treatment of Acne". To evaluate the safety and efficacy of the Cutera laser system for the treatment of acne vulgaris.

What is the current status of trial NCT06469398?

This trial is currently active not recruiting. It is a NA study. The enrollment target is 50 participants. The study started on 2022-07-21. Estimated completion is 2025-08-18.

What conditions does trial NCT06469398 study?

This clinical trial studies the following conditions: Acne Vulgaris.

What interventions are being tested in trial NCT06469398?

The interventions under investigation include: Cutera Laser System (DEVICE).

Who is sponsoring clinical trial NCT06469398?

This trial is sponsored by Cutera, which has 37 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT06469398 being conducted?

This trial has 3 study locations across Florida, New Jersey, Texas. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Similar trials for Acne Vulgaris

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 NCT06469398's enrollment target sits among peer trials

50 45th of 67 higher than 21 of 67 other Acne Vulgaris trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Acne Vulgaris 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

  • NCT00200889 · 50 participants · Early Phase 1

    Mapping Auricular Vagus Nerve Circuitry

  • NCT00409435 · 50 participants · Phase 2

    A Study of Pyridostigmine in Postural Tachycardia Syndrome

  • NCT01202305 · 50 participants

    The Use of Lymph Node Biopsies to Support HIV Pathogenesis Studies

  • NCT01225913 · 50 participants · Phase 4

    Mechanism(s) of Airflow Limitation During Exacerbation of Asthma

Similar registry start date

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

  • NCT07125183 · started 2026-12 · Phase 2

    Study on Efficacy and Tolerability of Weekly Doxorubicin in Elderly Patients With Advanced or Metastatic Leiomyosarcoma

  • NCT07292298 · started 2026-11 · Phase 2

    Phase 2 Single-Arm Rectal Cancer Brachytherapy for Patients With Low-Lying Residual Adenocarcinoma After Total Neoadjuvant Therapy to Improve Organ Preservation Rates

  • NCT04263285 · started 2026-10 · NA

    Treatment of Depression Post-SCI

Source: ClinicalTrials.gov NCT06469398, the US trial registry maintained by the National Library of Medicine. NCT06469398 (small enrollment · single site footprint · active not recruiting) retrieved and formatted by PlainTrial, see methodology.