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NCT05384093 · ClinicalTrials.gov registry record · NA
Outcomes of Treatment Using the ERMI Shoulder Flexionater ®
A NA study of Adhesive Capsulitis of Shoulder, sponsored by Foundation for Orthopaedic Research and Education.
- Recruiting
- Registry status
- NA
- Development phase
- 210
- Enrollment target
- 1
- Study location
NCT05384093: Recruiting NA study of Adhesive Capsulitis of Shoulder, sponsored by Foundation for Orthopaedic Research and Education.
NCT05384093 is a NA study of Adhesive Capsulitis of Shoulder that is actively recruiting participants, run by Foundation for Orthopaedic Research and Education. The registered enrollment target is 210 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (85% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT05384093, a NA study of Adhesive Capsulitis of Shoulder, is actively recruiting participants, sponsored by Foundation for Orthopaedic Research and Education.
- RECRUITING
- Registry status
- NA
- Development phase
- 210 participants
- Enrollment target
- 1
- Study location
Study Summary
Study 1 - Adhesive Capsulitis Study - 110 patients The purpose of this study is to compare treatment of patients with symptoms of adhesive capsulitis, primary and secondary, between three groups: I) Physical Therapy alone; II) ERMI Shoulder Flexionater® alone; III) PT + Device. Study 2 - Postoperative Shoulder Stiffness Study - 90 patients The purpose of this study is to compare treatment of patients with post-operative stiffness indicative of secondary adhesive capsulitis between three groups: I) Physical Therapy alone; II) ERMI Shoulder Flexionater® alone; III) PT + Device. Study 3 - Stiffness after MUA Study - enroll all eligible patients (goal of at least 15) The purpose of this study is to compare treatment of patients who have undergone manipulation under anesthesia or lysis of adhesions between three groups: I) Physical Therapy alone; II) ERMI Shoulder Flexionater® alone; III) PT + Device.
Primary Outcome
Measuring Shoulder External Rotation and Forward Flexion using a goniometer according to standard practice
Conditions Studied
Interventions
- DEVICE High Intensity Stretch Device
Study Locations (1)
Florida
- Foundation for Orthopaedic Research and Education - Tampa
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 210 participants |
| Start Date | 2019-06-25 |
| Est. Completion | 2026-06-25 |
| Phase | NA |
What NCT05384093 shows while recruiting
NCT05384093 is an interventional study that assigns participants to a tested intervention. The registered 210 participants enrollment target is mid-sized for trials with a published cap, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (85% lower).
The record links to 1 condition, with Adhesive Capsulitis of Shoulder appearing as the primary indexed condition, and to 1 intervention - of which High Intensity Stretch Device is the first listed.
NCT05384093 reports a single indexed study location in Florida.
Frequently Asked Questions
What is clinical trial NCT05384093 about?
NCT05384093 is a clinical study titled "Outcomes of Treatment Using the ERMI Shoulder Flexionater ®". Study 1 - Adhesive Capsulitis Study - 110 patients The purpose of this study is to compare treatment of patients with symptoms of adhesive capsulitis, primary and secondary, between three groups: I) Physical Therapy alone; II) ERMI Shoulder Flexionater® alone; III) PT + Device. Study 2 - Postoperat...
What is the current status of trial NCT05384093?
This trial is currently recruiting. It is a NA study. The enrollment target is 210 participants. The study started on 2019-06-25. Estimated completion is 2026-06-25.
What conditions does trial NCT05384093 study?
This clinical trial studies the following conditions: Adhesive Capsulitis of Shoulder.
What interventions are being tested in trial NCT05384093?
The interventions under investigation include: High Intensity Stretch Device (DEVICE).
Who is sponsoring clinical trial NCT05384093?
This trial is sponsored by Foundation for Orthopaedic Research and Education, which has 13 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT05384093 being conducted?
This trial has 1 study location across Florida. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
Learn More About Clinical Trials
Similar trials for Adhesive Capsulitis of Shoulder
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 NCT05384093's enrollment target sits among peer trials
210 490th of 2000 higher than 1,505 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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