Trial · NCT07914153
Early Functional Outcomes After Open Versus Percutaneous Repair of Acute Achilles Tendon Ruptures
NCT07914153, Not applicable, Not yet recruiting, University Hospital, Strasbourg, France
3 sourcestrials-2026-11-12-0.4.0
Cite this record
ConductScience Library. Early Functional Outcomes After Open Versus Percutaneous Repair of Acute Achilles Tendon Ruptures. Trials, record NCT07914153. Release trials-2026-11-12-0.4.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT07914153
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Early Functional Outcomes After Open Versus Percutaneous Repair of Acute Achilles Tendon Ruptures
- NCT number
- NCT07914153
- Status
- Not yet recruiting
- Phases
- Not applicable
- Enrollment
- 60 participants, estimated
- Lead sponsor
- University Hospital, Strasbourg, France
- Conditions
- Patients With an Acute Achilles Tendon Rupture, Time From Achilles Tendon Rupture to Surgery of Less Than 2 Weeks
- Interventions
- Percutaneous Surgical Repair of Acute Achilles Tendon Rupture, Open Surgical Repair of Acute Achilles Tendon Rupture
- First posted
- 2026-11-03
- Last updated
- 2026-11-03
Source ClinicalTrials.gov
Registered outcomes3
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Change in Achilles Tendon Total Rupture Score (ATRS) From 3 to 6 Months Postoperatively | 3 months and 6 months postoperatively. | The Achilles Tendon Total Rupture Score (ATRS) is a validated patient-reported outcome measure assessing symptoms and physical activity limitations following Achilles tendon rupture. The score ranges from 0 to 100 points, with higher scores indicating fewer symptoms and better function. The change in score will be calculated as the 6-month score minus the 3-month score and compared between the percutaneous surgery and open surgery groups. |
| Primary | Change in European Foot and Ankle Society (EFAS) Score From 3 to 6 Months Postoperatively | 3 months and 6 months postoperatively. | The European Foot and Ankle Society (EFAS) score is a patient-reported outcome measure assessing foot and ankle function. The score will be recorded using the questionnaire version specified in the study protocol, with a total score ranging from 0 to 40 points according to the study questionnaire. Higher scores indicate better function, provided this is consistent with the scoring instructions for the version used. The change in score will be calculated as the 6-month score minus the 3-month score and compared between the percutaneous surgery and open surgery groups. |
| Primary | Change in Return to Sport after Injury (RSI) Score From 3 to 6 Months Postoperatively | 3 months and 6 months postoperatively | Psychological readiness to return to sport will be assessed using a 12-item patient-reported questionnaire administered at 3 and 6 months postoperatively. Each item is rated from 0 to 10, giving a maximum raw total score of 120 points. Higher scores indicate greater psychological readiness to return to sport. The change in score will be calculated as the 6-month score minus the 3-month score and compared between patients undergoing percutaneous surgery and those undergoing open surgery. |
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.
Papers0
The papers the trial lists on ClinicalTrials.gov.
None in this release.
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/NCT07914153
GET https://conductscience.org/api/trials/v1/NCT07914153/registered