Trial · NCT07417449
Impact of Long-term Dutasteride Use on Perioperative Outcomes of HoLEP
NCT07417449, Recruiting, Ankara City Hospital Bilkent
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. Impact of Long-term Dutasteride Use on Perioperative Outcomes of HoLEP. Trials, record NCT07417449. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT07417449
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Impact of Long-term Dutasteride Use on Perioperative Outcomes of HoLEP
- NCT number
- NCT07417449
- Status
- Recruiting
- Enrollment
- 1,000 participants, estimated
- Lead sponsor
- Ankara City Hospital Bilkent
- Conditions
- Prostatic Hyperplasia, Benign
- Interventions
- Dutasteride, Holmium Laser Enucleation of the Prostate (HoLEP)
- First posted
- 2026-02-18
- Last updated
- 2026-11-04
Source ClinicalTrials.gov
Registered outcomes4
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Change in Hemoglobin Levels (Hemoglobin Drop) | From the time of hospital admission (preoperative) up to 24 hours after surgery. | The difference between preoperative hemoglobin levels and postoperative (first 24 hours) hemoglobin levels to assess surgical bleeding. |
| Secondary | Morcellation Efficiency Rate | During the surgical procedure (intraoperative). | The weight of the resected prostate tissue divided by the morcellation time. |
| Secondary | Total Operative Duration | During the surgical procedure (intraoperative). | Total time from the start of the enucleation to the completion of morcellation. |
| Secondary | Enucleation Efficiency | During the surgical procedure (intraoperative). | The weight of the resected tissue divided by the enucleation time. |
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/NCT07417449
GET https://conductscience.org/api/trials/v1/NCT07417449/registered