InMode MD

22 total trials 3 currently recruiting 19 completed

InMode MD sponsors 22 registered US clinical trials on ClinicalTrials.gov, 3 of them currently recruiting, and 19 completed. The most-studied condition in this pipeline is Premature Jowl and Neck Laxity Following Facialplasty, with 1 trials.

Trial Pipeline

22 total, page 1 of 1

RECRUITING NA

Detrusor Nerve Radiofrequency Ablation for Overactive Bladder in Women

NCT07209397

RECRUITING NA

Safety and Efficacy of Radio Frequency for the Treatment of Mild to Severe Inflammatory Acne

NCT05830968

RECRUITING NA

Evaluation of Safety and Efficacy of Morpheus8 Applicator for the Treatment of Focal Hyperhidrosis of the Axillae Using Radio Frequency

NCT05860972

COMPLETED NA

Transvaginal Radiofrequency Ablation for Overactive Bladder

NCT06458556

COMPLETED NA

RF Microneedling With Multi-Depth Targeting Per Insertion for The Treatment of Cellulite

NCT06283056

COMPLETED NA

Clinical Evaluation of Fractional Bi-Polar Radio-Frequency for Symptoms of Vulvovaginal Atrophy

NCT05398172

COMPLETED NA

Bi-Polar Radio-Frequency and Electrical Muscle Stimulation for Symptoms of Mixed Urinary Incontinence (MUI)

NCT05287490

COMPLETED NA

Clinical Evaluation of Fractional Bi-Polar RF for Symptoms of SUI and Vulvovaginal Atrophy

NCT04705571

COMPLETED NA

Trim II for Noninvasive Lipolysis and Circumference Reduction of Abdomen.

NCT05398159

COMPLETED NA

Treatment With the Evoke System for Facial and Submental Laxity

NCT04719013

COMPLETED NA

Evaluation of the Evoke Radiofrequency Device for Improvement of Skin Appearance

NCT04721600

COMPLETED

Retrospective Chart Review Study of Patients Treated With Votiva Device

NCT04437680

COMPLETED

Retrospective Evaluation of Cellulite of Laxity Treatment Using Body Tite

NCT04419454

COMPLETED NA

Radio Frequency (Forma Eye) Treatment for Dry Eye Disease Due to Meibomian Gland Dysfunction

NCT04120584

COMPLETED NA

Safety and Efficacy of Combined EMS and RF Treatments

NCT04124419

COMPLETED NA

Evoke Radiofrequency Device for Improvement of Skin Appearance

NCT04050033

COMPLETED NA

Energy-Based Lower Eyelid Rejuvenation - Proof of Concept for InMode AccuTite With or Without Morpheus8

NCT04103619

COMPLETED NA

The Use of RF in Premature Jowl and Neck Laxity Following Facialplasty

NCT03945422

COMPLETED NA

Evaluate the Effect of Abdominal Electrical Muscle Stimulation on Abdominal Wall Restoration in Post - Partum Women

NCT03917160

COMPLETED NA

Clinical Evaluation of CelluTite Treatment

NCT03769649

COMPLETED NA

Clinical Evaluation of RFAL of Breast Envelope and NAC Position

NCT03863834

COMPLETED NA

RF Rejuvenation for Pelvic Floor and Vagina

NCT03536819

What the Pipeline for InMode MD Shows

According to the ClinicalTrials.gov registry, InMode MD is linked to 22 US clinical trials across every stage of research activity. Of those, 3 studies are currently recruiting, about 14% of the sponsor's indexed portfolio, and 19 are already marked complete, representing roughly 86% of the total.

The phase mix for InMode MD reports 0 late-stage studies (Phase 3 and Phase 4 combined) and 0 earlier-phase studies (Phase 1 and Phase 2).

The top therapeutic focus area indexed for InMode MD is Premature Jowl and Neck Laxity Following Facialplasty with 1 linked trial, and 9 other condition areas appear in the top list above.

How to read these pipeline numbers

Recruiting share is one of the more practical signals here: it reflects how much of a sponsor's research is presently open to new participants, while the completed share indicates the depth of finished work that has already contributed registry results. Both counts come directly from the public ClinicalTrials.gov dataset and are refreshed on the registry side; this page mirrors the latest data pull without altering it.

A portfolio weighted toward Phase 3 usually reflects an organization advancing candidates toward regulatory review, where the research centers on comparative efficacy and broader safety across larger populations. A heavier Phase 1 and Phase 2 tilt generally indicates exploratory work, safety, dosing, and early signal detection, and is common among research-forward sponsors that seed many early programs. Phase 4 entries, when present, track interventions already in real-world use and typically focus on long-term safety, effectiveness across subgroups, or formulation comparisons.

That distribution is a quick read of where the organization concentrates its research attention; it does not imply product availability, market share, or any clinical endorsement. All numbers on this page come from ClinicalTrials.gov maintained by the National Library of Medicine, and counts can shift as new studies are registered or existing ones update their status. This information is provided for reference and educational purposes only, not as medical, investment, or regulatory advice, verify current details directly with ClinicalTrials.gov before relying on any figure here.

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page aggregates every registered trial from this sponsor, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.