Trial · NCT07891013
Posterior Pericapsular Deep-gluteal Block
NCT07891013, Not applicable, Not yet recruiting, Ankara Etlik City Hospital
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. Posterior Pericapsular Deep-gluteal Block. Trials, record NCT07891013. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT07891013
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Posterior Pericapsular Deep-gluteal Block
- NCT number
- NCT07891013
- Status
- Not yet recruiting
- Phases
- Not applicable
- Enrollment
- 60 participants, estimated
- Lead sponsor
- Ankara Etlik City Hospital
- Conditions
- Pain, Postoperative
- Interventions
- PENG (Pericapsular nerve group) block, LFCN (Lateral femoral cutaneous nerve) block, PPD (Posterior pericapsular deep gluteal) block
- First posted
- 2026-10-23
- Last updated
- 2026-10-23
Source ClinicalTrials.gov
Registered outcomes8
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | 6-hour dynamic pain intensity | 6 hours postoperatively | Dynamic pain will be assessed using the Numerical Rating Scale (NRS), ranging from 0 (no pain) to 10 (worst imaginable pain). |
| Secondary | Dynamic pain intensity | 4, 8, 12, and 24 hours postoperatively | Dynamic pain will be assessed using the Numerical Rating Scale (NRS), ranging from 0 (no pain) to 10 (worst imaginable pain). |
| Secondary | Pain intensity at rest | 4, 6, 8, 12, and 24 hours postoperatively | Resting pain will be assessed using the Numerical Rating Scale (NRS), ranging from 0 (no pain) to 10 (worst imaginable pain). |
| Secondary | Cumulative morphine consumption | Up to 24 hours postoperatively | The cumulative amount of morphine consumed during the first 24 hours postoperatively will be recorded in milligrams (mg). |
| Secondary | Time to first rescue analgesic | Up to 24 hours postoperatively | The time from the end of surgery to the first pain score ≥ 4 at rest or during movement, or to the first patient request for analgesia, will be recorded in hours. |
| Secondary | Quality of Recovery (QoR)-15 score | Preoperatively and postoperative day 1 | Quality of postoperative recovery will be assessed using the 15-item Quality of Recovery (QoR-15) questionnaire. The total score ranges from 0 to 150, with higher scores indicating better quality of recovery. |
| Other | Patient satisfaction score | Postoperative day 1 | Patient satisfaction with postoperative pain management will be assessed using a numerical rating scale ranging from 0 (completely dissatisfied) to 10 (completely satisfied), with higher scores indicating greater satisfaction. |
| Other | Sleep quality score | Postoperative day 1 | Sleep quality during the first postoperative night will be assessed using a 5-point numerical rating scale ranging from 1 (very poor) to 5 (very good), with higher scores indicating better sleep quality. |
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/NCT07891013
GET https://conductscience.org/api/trials/v1/NCT07891013/registered