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

NCT06274177 · ClinicalTrials.gov registry record · NA

Evaluation of the BTL-785F Device for Submental Fat Reduction and Neck Rejuvenation

A NA study, sponsored by BTL Industries.

Completed
Registry status
NA
Development phase
37
Enrollment target

NCT06274177: Completed NA study, sponsored by BTL Industries.

NCT06274177 is a NA study that has completed, run by BTL Industries. The registered enrollment target is 37 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (97% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT06274177, a NA study, has completed, sponsored by BTL Industries.

COMPLETED
Registry status
NA
Development phase
37 participants
Enrollment target

Study Summary

This study will evaluate the clinical safety and the performance of the BTL-785F system equipped with the BTL-785-7 applicator for non-invasive reduction of submental fat and skin laxity treatment.

Primary Outcome

The primary efficacy outcome measure is a statistically significant reduction of at least 1.0 mm in the average submental fat layer thickness in the majority of subjects measured by MRI at 3-months follow-up compared to baseline.

Interventions

  • DEVICE BTL-785-7

Trial Details

FieldValue
Enrollment Target 37 participants
Start Date 2023-07-26
Est. Completion 2024-09-12
Phase NA
BTL Industries

40 total trials

What the finished NCT06274177 record still lists

NCT06274177 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 37 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (97% lower).

The record links to 0 conditions, and to 1 intervention - of which BTL-785-7 is the first listed.

NCT06274177 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT06274177 about?

NCT06274177 is a clinical study titled "Evaluation of the BTL-785F Device for Submental Fat Reduction and Neck Rejuvenation". This study will evaluate the clinical safety and the performance of the BTL-785F system equipped with the BTL-785-7 applicator for non-invasive reduction of submental fat and skin laxity treatment.

What is the current status of trial NCT06274177?

This trial is currently completed. It is a NA study. The enrollment target is 37 participants. The study started on 2023-07-26. Estimated completion is 2024-09-12.

What interventions are being tested in trial NCT06274177?

The interventions under investigation include: BTL-785-7 (DEVICE).

Who is sponsoring clinical trial NCT06274177?

This trial is sponsored by BTL Industries, which has 40 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT06274177's enrollment target sits among peer trials

37 1540th of 2000 higher than 460 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

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

  • NCT02800486 · 37 participants · Phase 2

    Super Selective Intra-arterial Repeated Infusion of Cetuximab (Erbitux) With Reirradiation for Treatment of Relapsed/Refractory GBM, AA, and AOA

  • NCT03173937 · 37 participants · Phase 1

    Unrelated Umbilical Cord Blood Transplantation for Severe Aplastic Anemia and Hypo-plastic MDS Using CordIn(TM), Umbilical Cord Blood-Derived Ex Vivo Expanded Stem and Progenitor Cells to Expedite Engraftment and Improve Transplant Outcome

  • NCT03295227 · 37 participants · Phase 1

    Pembrolizumab in Treating Participants With Unresectable Thymoma or Thymic Cancer

  • NCT03401047 · 37 participants · Early Phase 1

    Study to Assess Potential Impairments in Estradiol Augmentation of Gonadotropin Secretion in Polycystic Ovary Syndrome

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 NCT06274177, the US trial registry maintained by the National Library of Medicine. NCT06274177 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.