Trial · NCT07892729
Outcomes of Arthroscopic Dynamic Anterior Stabilization With and Without Remplissage
NCT07892729, Active not recruiting, Omniartro Lda
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. Outcomes of Arthroscopic Dynamic Anterior Stabilization With and Without Remplissage. Trials, record NCT07892729. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT07892729
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Outcomes of Arthroscopic Dynamic Anterior Stabilization With and Without Remplissage
- NCT number
- NCT07892729
- Status
- Active not recruiting
- Enrollment
- 41 participants, estimated
- Lead sponsor
- Omniartro Lda
- Conditions
- Anterior Shoulder Instability
- Interventions
- Arthroscopic Onlay Dynamic Anterior Stabilization Using the Long Head of the Biceps Tendon (DAS-LHB), Hill-Sachs Remplissage
- First posted
- 2026-10-23
- Last updated
- 2026-10-23
Source ClinicalTrials.gov
Registered outcomes9
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Change in Western Ontario Shoulder Instability Index (WOSI) score | From preoperative baseline to a minimum of 24 months after surgery | The Western Ontario Shoulder Instability Index (WOSI) is a patient-reported outcome measure specific to shoulder instability. The total score ranges from 0 to 2100, with lower scores indicating better shoulder-related quality of life and fewer symptoms. The primary outcome is the within-participant change in WOSI score from the preoperative assessment to the final follow-up assessment. |
| Secondary | Change in Rowe score | From Preoperative baseline to a minimum of 24 months after surgery | The Rowe score is a clinician-reported outcome measure used to assess shoulder stability, function, and motion after treatment for anterior shoulder instability. The total score ranges from 0 to 100, with higher scores indicating better shoulder function and stability. The outcome is the within-participant change in Rowe score from the preoperative assessment to final follow-up. |
| Secondary | Change in shoulder range of motion | From Preoperative baseline to a minimum of 24 months after surgery | Active shoulder range of motion will be assessed using routinely recorded clinical measurements, including forward flexion, abduction, external rotation with the arm at the side, and internal rotation. The outcome is the change from preoperative values to final follow-up. |
| Secondary | Recurrent anterior shoulder instability | From index surgery to final follow-up, minimum 24 months | Recurrent instability will include postoperative dislocation and subluxation events of the operated shoulder. The proportion of participants experiencing recurrent anterior instability after the index procedure will be reported. |
| Secondary | Positive anterior apprehension test | At final follow-up, minimum 24 months after surgery | The anterior apprehension test will be assessed at final clinical follow-up. The outcome will be the proportion of participants with a positive apprehension test, indicating persistent apprehension or instability symptoms. |
| Secondary | Structural integrity and healing of the transferred long head of the biceps tendon on MRI | Postoperative MRI obtained at least 6 months after surgery | Postoperative shoulder MRI examinations will be reviewed to assess the transferred long head of the biceps tendon at the anterior glenoid fixation site. The tendon will be classified according to as intact/healed, partially failed, or completely failed. |
| Secondary | Reoperation rate | From index surgery to final follow-up, minimum 24 months | The proportion of participants requiring any subsequent surgical procedure on the operated shoulder after the index DAS-LHB procedure will be reported, including surgery performed for recurrent instability or other postoperative complications. |
| Secondary | Return to sport | From index surgery to final follow-up, minimum 24 months | Return to sport after surgery will be assessed from the clinical record and follow-up information. Outcomes will include return to any sport and return to the same sport and level of participation as before the onset of instability, where these data are available. |
| Secondary | Biceps-related clinical findings | At final follow-up, minimum 24 months after surgery | Postoperative biceps-related findings will include Popeye deformity, biceps cramping, and tenderness of the bicipital groove. These findings will be reported and explored in relation to postoperative MRI findings of the transferred long head of the biceps tendon. |
Source ClinicalTrials.gov
Outcomes0
Each outcome the trial posted results for, in ClinicalTrials.gov's words.
None in this release.
Results by group0
Each measurement the trial posted, group by group, in the words and numbers it posted.
None in this release.
Participant flow0
How many started, completed or left each group, period by period.
None in this release.
Adverse events0
Each adverse event the trial posted, group by group: the participants affected out of those at risk.
None in this release.
Adverse event totals0
The totals the trial posted for each group.
None in this release.
Papers3
The papers the trial lists on ClinicalTrials.gov.
Grants0
The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.
None in this release.
Trial comparisons0
Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.
None in this release.
Tests0
The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.
None in this release.
Data dates
The day each source was copied for this release.
Sources 3
- ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
- ClinicalTrials.govNo license stated
- NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
- ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
- ClinicalTrials.govnone stated
- NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)
ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
For software
Read this trial from software.
The record and each of its lists are JSON, twenty rows a page. No key.
GET https://conductscience.org/api/trials/v1/NCT07892729
GET https://conductscience.org/api/trials/v1/NCT07892729/registered