Trial · NCT07879521
PENG, Suprainguinal Fascia Iliaca Block, and Control After Total Hip Arthroplasty
NCT07879521, Not applicable, Completed, Uludag University
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. PENG, Suprainguinal Fascia Iliaca Block, and Control After Total Hip Arthroplasty. Trials, record NCT07879521. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT07879521
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- PENG, Suprainguinal Fascia Iliaca Block, and Control After Total Hip Arthroplasty
- NCT number
- NCT07879521
- Status
- Completed
- Phases
- Not applicable
- Enrollment
- 99 participants, actual
- Lead sponsor
- Uludag University
- Conditions
- Total Hip Arthroplasty, Postoperative Pain
- Interventions
- Pericapsular nerve group (PENG) block, Suprainguinal Fascia Iliaca Plane Block
- First posted
- 2026-10-19
- Last updated
- 2026-10-19
Source ClinicalTrials.gov
Registered outcomes3
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Postoperative Pain Scores | Up to 24 hours after surgery. | Postoperative pain intensity was assessed using the visual analog scale (VAS), with scores recorded on a 0-100 mm scale. Pain scores were compared among the PENG block, suprainguinal fascia iliaca plane block, and control groups. |
| Secondary | Quadriceps Muscle Strength | Up to 24 hours after surgery. | Quadriceps muscle strength was assessed using manual muscle testing (MMT). |
| Secondary | Hip Flexion Angle | Up to 24 hours after surgery. | Hip flexion angle was measured in degrees. |
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/NCT07879521
GET https://conductscience.org/api/trials/v1/NCT07879521/registered