Trial · NCT07911501
Perioperative Dutasteride for Hemorrhage Control in Bipolar TURP Under Anticoagulation.
NCT07911501, Phase 4, Not yet recruiting, Mohamed Mahmoud Dogha
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. Perioperative Dutasteride for Hemorrhage Control in Bipolar TURP Under Anticoagulation. Trials, record NCT07911501. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT07911501
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Perioperative Dutasteride for Hemorrhage Control in Bipolar TURP Under Anticoagulation.
- NCT number
- NCT07911501
- Status
- Not yet recruiting
- Phases
- Phase 4
- Enrollment
- 44 participants, estimated
- Lead sponsor
- Mohamed Mahmoud Dogha
- Conditions
Benign Prostatic Hyperplasia, Postoperative Hemorrhage, Perioperative Hemorrhage Control During Bipolar Transurethral Resection of the Prostate (TURP) in Patients on Anticoagulant or Antiplatelet Therapy
- Interventions
- Dutasteride (0.5mg), Placebo
- First posted
- 2026-11-02
- Last updated
- 2026-11-02
Source ClinicalTrials.gov
Registered outcomes8
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Change in Hemoglobin (Hb) Level | Baseline (preoperative), immediately postoperatively, and 24 hours postoperatively. | Mean difference in serum Hb (g/dL) from baseline. |
| Primary | Change in Hematocrit (Hct) Level | Baseline (preoperative), immediately postoperatively, and 24 hours postoperatively. | Mean difference in Hct from baseline. |
| Secondary | Total Volume of Bladder Irrigation Fluid | Postoperative until 24 hrs. | Total volume of 0.9% normal saline used (liters). |
| Secondary | Duration of Bladder Irrigation | Postoperative time: 24 hours. | Total time of continuous bladder irrigation (hours). |
| Secondary | Indwelling Catheterization Duration | 5-8 day postoperative | Total duration of urethral catheterization (days). |
| Secondary | Length of Hospital Stay | From day of surgery to 7 days postoperative. | Postoperative hospital duration (days). |
| Secondary | Incidence of Postoperative Complications | Intraoperative through 1-month follow-up. | Rates of clot retention, severe hematuria requiring re-intervention, blood transfusion, or reoperation. |
| Secondary | Symptomatic & Functional Improvements | Baseline vs. 1-month postoperatively. | Changes in International Prostate Symptom Score (IPSS) and Post-Void Residual (PVR) urine volume (mL). |
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/NCT07911501
GET https://conductscience.org/api/trials/v1/NCT07911501/registered