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HIFEM and Radiofrequency for Muscular System Function Improvement
NCT06703749 · View on ClinicalTrials.gov ↗
Study Summary
The goal of this clinical trial is to investigate the effect of the BTL-899M device on muscular system function in adult subjects seeking treatment for improving their muscular system function in the lower extremities. The main question it aims to answer is: Whether the BTL-899M device is effective for muscular system function improvement 3 months posttreatment compared to the sham group, based on the dynamometer measurement. Researchers will compare a sham group to see if the device is effective. Participants will complete four treatment visits and two follow-up visits. Their strength will be recorded via a dynamometer.
Conditions Studied
Interventions
- DEVICE Treatment with BTL-899M
- DEVICE Treatment with BTL-899M with intensities below therapeutic threshold
Study Locations (3)
Arizona
- Royal Spine Surgery — Scottsdale
Colorado
- The Longevity Lab — Greenwood Village
Florida
- Saville Spine Institute — Palm Beach Gardens
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 33 participants |
| Start Date | 2024-04-22 |
| Est. Completion | 2025-06 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT06703749
The ClinicalTrials.gov registry entry for NCT06703749 describes a study currently listed as active not recruiting. It is categorized as NA, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 33 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is BTL Industries, which has 9 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.
The record links to 3 conditions, with Muscle Weakness appearing as the primary indexed condition, and to 2 interventions — of which Treatment with BTL-899M is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.
Geographic footprint matters for practical reasons: NCT06703749 reports 3 study locations spanning 3 distinct geographic areas — top geographies include Arizona, Colorado, Florida. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.
Frequently Asked Questions
What is clinical trial NCT06703749 about?
NCT06703749 is a clinical study titled "HIFEM and Radiofrequency for Muscular System Function Improvement". The goal of this clinical trial is to investigate the effect of the BTL-899M device on muscular system function in adult subjects seeking treatment for improving their muscular system function in the lower extremities. The main question it aims to answer is: Whether the BTL-899M device is effective...
What is the current status of trial NCT06703749?
This trial is currently active not recruiting. It is a NA study. The enrollment target is 33 participants. The study started on 2024-04-22. Estimated completion is 2025-06.
What conditions does trial NCT06703749 study?
This clinical trial studies the following conditions: Muscle Weakness, Muscle Damage, Muscle Strength. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT06703749?
The interventions under investigation include: Treatment with BTL-899M (DEVICE), Treatment with BTL-899M with intensities below therapeutic threshold (DEVICE). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT06703749?
This trial is sponsored by BTL Industries, which has 9 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT06703749 being conducted?
This trial has 3 study locations across Arizona, Colorado, Florida. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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