Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.
NCT01241916 · ClinicalTrials.gov registry record · NA
A Prospective Randomized Trial of Static-Progressive Versus Dynamic Splinting for Post-Traumatic Elbow Stiffness
A NA study of Post-traumatic Stiff Elbows, sponsored by Massachusetts General Hospital.
- Completed
- Registry status
- NA
- Development phase
- 66
- Enrollment target
- 1
- Study location
NCT01241916: Completed NA study of Post-traumatic Stiff Elbows, sponsored by Massachusetts General Hospital.
NCT01241916 is a NA study of Post-traumatic Stiff Elbows that has completed, run by Massachusetts General Hospital. The registered enrollment target is 66 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (95% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT01241916, a NA study of Post-traumatic Stiff Elbows, has completed, sponsored by Massachusetts General Hospital.
- COMPLETED
- Registry status
- NA
- Development phase
- 66 participants
- Enrollment target
- 1
- Study location
Study Summary
Primary Question: "When splinting is used to improve motion in post-traumatic stiff elbows, is there a significant difference in gains in motion achieved between static progressive or dynamic splint approaches?" Secondary Question: "Is there a significant difference in patient compliance with static progressive versus dynamic splint use, and does this effect final ulnohumeral motion outcomes?"
Primary Outcome
Active ulnohumeral motion will be measured using a hand-held goniometer by the co-investigator not involved in the care of the patient at enrollment and 6 months after enrollment.
Conditions Studied
Interventions
- DEVICE Static-Progressive Splint
- DEVICE Dynamic Splint
Study Locations (1)
Massachusetts
- Massachusetts General Hospital - Boston
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 66 participants |
| Start Date | 2003-08 |
| Est. Completion | 2010-09 |
| Phase | NA |
What the finished NCT01241916 record still lists
NCT01241916 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 66 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (95% lower).
The record links to 1 condition, with Post-traumatic Stiff Elbows appearing as the primary indexed condition, and to 2 interventions - of which Static-Progressive Splint is the first listed.
NCT01241916 reports a single indexed study location in Massachusetts.
Frequently Asked Questions
What is clinical trial NCT01241916 about?
NCT01241916 is a clinical study titled "A Prospective Randomized Trial of Static-Progressive Versus Dynamic Splinting for Post-Traumatic Elbow Stiffness". Primary Question: "When splinting is used to improve motion in post-traumatic stiff elbows, is there a significant difference in gains in motion achieved between static progressive or dynamic splint approaches?" Secondary Question: "Is there a significant difference in patient compliance with stati...
What is the current status of trial NCT01241916?
This trial is currently completed. It is a NA study. The enrollment target is 66 participants. The study started on 2003-08. Estimated completion is 2010-09.
What conditions does trial NCT01241916 study?
This clinical trial studies the following conditions: Post-traumatic Stiff Elbows.
What interventions are being tested in trial NCT01241916?
The interventions under investigation include: Static-Progressive Splint (DEVICE), Dynamic Splint (DEVICE).
Who is sponsoring clinical trial NCT01241916?
This trial is sponsored by Massachusetts General Hospital, which has 2,032 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT01241916 being conducted?
This trial has 1 study location across Massachusetts. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT01241916's enrollment target sits among peer trials
66 1139th of 2000 higher than 857 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
- NCT02584244 · 66 participants · Phase 1
Feasibility of the LUM Imaging System for Detection of Gastrointestinal Cancers
- NCT03067051 · 66 participants · Phase 1
Clinical Study to Assess the Safety and Efficacy of the SpectraCure P18 System
- NCT03754725 · 66 participants · Phase 1
Ferritin and Iron Burden in SAH sIRB
- NCT03875378 · 66 participants · Phase 2
Transdermal Estrogen in Women With Anorexia Nervosa
Similar registry start date
- NCT05988463 · started 2027-01-01 · Phase 1
Dose-Escalation Study of Artesunate Patients With IPF
- NCT07219706 · started 2026-12-10 · NA
Dietary Fiber and Time Restricted Eating
- NCT02831335 · started 2026-12-01
Technical Development of Multi-Parametric Renocerebral MRI
- NCT05962346 · started 2026-12 · NA
Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia