Trial · NCT07877974
Efficacy of Gastrocnemius Plane Block for Foot and Ankle Surgery
NCT07877974, Not applicable, Recruiting, Cairo University
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. Efficacy of Gastrocnemius Plane Block for Foot and Ankle Surgery. Trials, record NCT07877974. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT07877974
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Efficacy of Gastrocnemius Plane Block for Foot and Ankle Surgery
- NCT number
- NCT07877974
- Status
- Recruiting
- Phases
- Not applicable
- Enrollment
- 40 participants, estimated
- Lead sponsor
- Cairo University
- Conditions
- Gastrocnemius, Ankle Surgery, Foot Surgery, Postoperative Analgesia
- Interventions
- GPB Group : This group will receive ultrasound-guided Gastrocnemius plane block with 30 mL bupivacaine (0.25%), SAB
- First posted
- 2026-10-16
- Last updated
- 2026-10-16
Source ClinicalTrials.gov
Registered outcomes9
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Time to first postoperative analgesic request | 24 hours | Time to first postoperative analgesic request |
| Secondary | Visual analogue pain score (VAS) | 24 hours | Visual analogue pain score (VAS) at rest (static), and on movement (dynamic) at 2, 4, 6, 12, 18, and 24 hours postoperatively |
| Secondary | Postoperative assessment of sensory and motor function | 24 hours | Assessment of sensory block: Sensory block will be assessed using a pinprick test with a blunt 22-gauge needle along dermatomes relevant to the surgery. The degree of sensory loss will be graded as follows: * Grade 0: Normal sensation to pinprick * Grade 1: Decreased but present sensation to pinprick (hypoalgesia) * Grade 2: Complete loss of sensation to pinprick (analgesia) |
| Secondary | Time to first postoperative analgesic request | 24 hours | Time to first postoperative analgesic request |
| Secondary | Total morphine requirements | 24 hours | Total morphine requirements 24 hours postoperatively. |
| Secondary | Time to early mobilization | 24 hours | Time to early mobilization: First bedtime helps to judge the effect of the nerve block |
| Secondary | Incidence of complications related to the blocks | 24 hours | Incidence of complications related to the blocks as hematoma or Toxicity |
| Secondary | Incidence of postoperative nausea and vomiting | 24 hours | Incidence of postoperative nausea and vomiting |
| Secondary | Postoperative assessment of motor function | 24 hours | Assessment of motor block: using the Modified Bromage score, which will be evaluated to assess the motor block as follows: * Bromage 0: full flexion of the knee and feet. * Bromage 1: just able to move the knee * Bromage 2: able to move the feet. * Bromage 3: unable to move the knees and feet |
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/NCT07877974
GET https://conductscience.org/api/trials/v1/NCT07877974/registered