Trial · NCT07890831
Dermis on Demand Allograft Augmentation for Rotator Cuff Repair
NCT07890831, Not applicable, Completed, University of Cincinnati
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. Dermis on Demand Allograft Augmentation for Rotator Cuff Repair. Trials, record NCT07890831. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT07890831
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Dermis on Demand Allograft Augmentation for Rotator Cuff Repair
- NCT number
- NCT07890831
- Status
- Completed
- Phases
- Not applicable
- Enrollment
- 60 participants, actual
- Lead sponsor
- University of Cincinnati
- Conditions
- Rotator Cuff Tears, Rotator Cuff Injuries
- Interventions
- Arthroscopic rotator cuff repair; Biological: Dermis on Demand, Arthroscopic rotator cuff repair
- First posted
- 2026-10-22
- Last updated
- 2026-10-22
Source ClinicalTrials.gov
Registered outcomes11
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Rotator cuff retear rate | 12 months postoperatively | Proportion of participants with a retear on MRI, defined as Sugaya type IV or V (scale I-V; higher = worse integrity) |
| Secondary | MRI rotator cuff score | 12 months | Sum of footprint size, tendon thickness, and signal intensity, each graded 1-4 (Crim et al., 2010). Total range 3-12; 12 = normal tendon. |
| Secondary | Fatty infiltration | 12 months | Goutallier grade 0-4 (higher = more fatty infiltration) |
| Secondary | Ultrasound repair integrity | 6 months | Proportion with intact repair on shoulder ultrasound |
| Secondary | ASES score | Baseline, 6 wk, 3, 6, 12 months | American Shoulder and Elbow Surgeons score, 0-100 (higher = better) |
| Secondary | SANE score | Baseline, 6 wk, 3, 6, 12 months | Single Assessment Numeric Evaluation, 0-100% (higher = better) |
| Secondary | PROMIS Upper Extremity | Baseline, 6 wk, 3, 6, 12 months | T-score, population mean 50, SD 10 (higher = better function) |
| Secondary | SF-12 | Baseline, 6 wk, 3, 6, 12 months | Physical and Mental Component Summary scores, norm-based, mean 50 (higher = better) |
| Secondary | Shoulder range of motion | Baseline, 6 wk, 3, 6, 12 months | Forward flexion, abduction, external and internal rotation, in degrees |
| Secondary | Shoulder strength | Baseline, 6 wk, 3, 6, 12 months | Manual muscle testing, graded 0-5 |
1 to 10 of 11Source ClinicalTrials.gov
See all 11 registered outcomesOutcomes0
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/NCT07890831
GET https://conductscience.org/api/trials/v1/NCT07890831/registered