Trial · NCT07907653
Registered outcomes21
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
21 to 21 of 21
Download this page as JSON| List | Outcome | Time frame | Description |
|---|---|---|---|
| Secondary | Incidence and Severity of Postoperative Complications | From radical prostatectomy through the adjuvant baseline visit (approximately 4 weeks postoperatively), with additional assessment at adjuvant Week 4 (approximately 8 weeks postoperatively) as clinically indicated. | Percentage of participants undergoing radical prostatectomy who experience at least one postoperative complication. Complications are summarized by type and severity using the National Cancer Institute Common Terminology Criteria for Adverse Events (NCI-CTCAE) version 6.0, with investigator clinical judgment for events not specifically covered by CTCAE. |
Source ClinicalTrials.govtrials-2026-11-12-0.5.0
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 list from software.
Twenty rows a page, as JSON. No key.
GET https://conductscience.org/api/trials/v1/NCT07907653/registered?page=2