Trial · NCT07901205
Use of Bioresorbable Magnesium Set Screws in Syndesmotic Injuries: a Pilot Study
NCT07901205, Recruiting, Patrick Lukas Holweg, MD
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. Use of Bioresorbable Magnesium Set Screws in Syndesmotic Injuries: a Pilot Study. Trials, record NCT07901205. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT07901205
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Use of Bioresorbable Magnesium Set Screws in Syndesmotic Injuries: a Pilot Study
- NCT number
- NCT07901205
- Status
- Recruiting
- Enrollment
- 20 participants, estimated
- Lead sponsor
- Patrick Lukas Holweg, MD
- Conditions
- Syndesmotic Injury, Trimalleolar Fracture, Bimalleolar Ankle Fracture, Osteosynthesis, Magnesium
- First posted
- 2026-10-28
- Last updated
- 2026-10-28
Source ClinicalTrials.gov
Registered outcomes9
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | implant function | 12 weeks and 1 year postoperatively | Successful temporary maintenance of stable pedicle screw fixation with ZX00 without intraoperative technical problems or change of fixation method. |
| Secondary | pain releave | baseline, 12 weeks and 1 year postoperatively | visual analoge scale |
| Secondary | functional improvement | baseline, 12 weeks and 1 year postoperatively | AOFAS-Score |
| Secondary | Subjective performance capacity | baseline, 12 weeks and 1 year postoperatively | FAAM-Score |
| Secondary | Radiological durability | 12 weeks and 1 year postoperatively | no secondary displacement on plain radiographs in two planes |
| Secondary | Complication rate | 12 weeks and 1 year postoperatively | occurrence of mechanical irritation, implant-associated wound healing disorder, or premature material failure |
| Secondary | Osseointegration | 12 weeks and 1 year postoperatively | radiological assessment of bony consolidation based on CT control |
| Secondary | Reoperation rate | 1 year postoperatively | |
| Secondary | Health economic aspects | 1 year postoperatively | (e.g. avoided implant removals / reduced need for hardware removal 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/NCT07901205
GET https://conductscience.org/api/trials/v1/NCT07901205/registered