Trial · NCT07889869
Ultrasound-Guided Versus Landmark-Guided Pudendal Block for Post-Hemorrhoidectomy Pain
NCT07889869, Not applicable, Enrolling by invitation, Konya City Hospital
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. Ultrasound-Guided Versus Landmark-Guided Pudendal Block for Post-Hemorrhoidectomy Pain. Trials, record NCT07889869. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT07889869
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Ultrasound-Guided Versus Landmark-Guided Pudendal Block for Post-Hemorrhoidectomy Pain
- NCT number
- NCT07889869
- Status
- Enrolling by invitation
- Phases
- Not applicable
- Enrollment
- 80 participants, estimated
- Lead sponsor
- Konya City Hospital
- Conditions
- Hemorrhoids, Postoperative Pain, Pudendal Nerve Block
- Interventions
- Ultrasound-Guided Pudendal Nerve Block, Landmark-Guided Pudendal Nerve Block
- First posted
- 2026-10-22
- Last updated
- 2026-10-22
Source ClinicalTrials.gov
Registered outcomes6
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Postoperative Pain Intensity at 24 Hours | 24 hours after surgery | Postoperative pain intensity will be assessed using a Visual Analog Scale (VAS) ranging from 0 (no pain) to 10 (worst imaginable pain). |
| Secondary | Postoperative Pain Intensity at 6, 12, and 48 Hours | 6, 12, and 48 hours after surgery | Postoperative pain intensity will be assessed using a Visual Analog Scale (VAS) ranging from 0 (no pain) to 10 (worst imaginable pain). |
| Secondary | Total Postoperative Analgesic Consumption | Within 48 hours after surgery | Total rescue analgesic consumption during the first 48 hours after surgery will be recorded and compared between study groups. |
| Secondary | Incidence of Early Postoperative Complications | Within 48 hours after surgery | The incidence of urinary retention and postoperative nausea and vomiting occurring during the first 48 hours after surgery will be recorded. |
| Secondary | Patient Satisfaction | 48 hours after surgery | Patient satisfaction with postoperative pain management will be assessed at 48 hours after surgery using a 5-point Likert scale, with higher scores indicating greater satisfaction. |
| Secondary | Quality of Postoperative Recovery | 48 hours after surgery | Quality of postoperative recovery will be assessed at 48 hours after surgery using the Quality of Recovery-15 (QoR-15) questionnaire. The questionnaire consists of 15 items, with a total score ranging from 0 to 150. Higher scores indicate better postoperative recovery. |
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.
Papers5
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/NCT07889869
GET https://conductscience.org/api/trials/v1/NCT07889869/registered