NCT07787442

CompletedPhase 1

Postoperative Pain Management for Hip Surgeries: UltrasoundG...

Ain Shams University Source

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Other study identifiers

Sponsor study identifier

FMASU MS 763/2025

Study Type

interventional

Actual enrollment (reported)

30

Locations

1 country

Sites

1

Timeline

Study Start

November 2, 2025

Actual (reported)

Primary Completion

May 2, 2026

Actual (reported)

Study Completion

June 2, 2026

Actual (reported)

Brief Summary

The aim of the Study is to compare the analgesic efficacy and clinical outcomes of suprainguinal fascia iliaca block (SIFIB) alone versus SIFIB combined with sciatic nerve block (SNB) in patients undergoing hip surgery.

Registry Overview

Registry-reported information. Elapsed time and enrollment totals alone do not measure study progress or recruitment pace.

Recruitment status: completed
Actual enrollment (reported): 30 participants
Study completion date: June 2, 2026
Actual (reported)
Listed locations: 1 countries · 1 sites

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Dates and qualifiers reported by the registry. Estimated dates do not confirm that a milestone has occurred.

Study Start
November 2, 2025
Actual (reported)
Primary Completion
May 2, 2026
Actual (reported)
Study Completion
June 2, 2026
Actual (reported)
First Submitted
August 23, 2026
Actual (reported)
First Posted
August 26, 2026
Actual (reported)

Last Updated: August 26, 2026
Status Verified: August 2026
Last Update Submitted: August 23, 2026

Conditions

Postoperative Pain

Outcome Measures

Primary Outcomes (1)

Time for first rescue analgesia
Time to first request for rescue analgesia: Defined as the time interval from the end of procedure until the patient's first complaint of pain with a Numerical Rating Scale (NRS) score ≥ 4 and requests pain relief
Numerical Pain Score in PACU, 6 hrs, 12 hrs, 24 hrs and 48 hrs postoperative

Secondary Outcomes (1)

Motor Block Assessment
The Modified Bromage Scale at 2 , 6 , 12 and 24 hours postoperatively

Study Arms (2)

Ultrasound Guided Suprainguinal Fascia Iliaca Compartment Block

ACTIVE COMPARATOR

Drug: Bupivacaine injection

Ultrasound Guided Suprainguinal Fascia Iliaca Compartment Block in combination with Sciatic Nerve Bl

ACTIVE COMPARATOR

Drug: Bupivacaine injection

Interventions

Bupivacaine injectionDrug

Bupivacaine injection

Ultrasound Guided Suprainguinal Fascia Iliaca Compartment BlockUltrasound Guided Suprainguinal Fascia Iliaca Compartment Block in combination with Sciatic Nerve Bl

Eligibility Criteria

Age18 Years - 70 Years

Sexall

Healthy VolunteersNo

Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

Age: 18 - 70 years old.
Sex: Both sexes.

Sponsors & Collaborators

Ain Shams University
Otherlead

Study Sites (1)

Ain Shams University

Cairo, Abbassia, 00202, Egypt

MeSH Terms

Conditions

Pain, Postoperative

Interventions

Bupivacaine

Condition Hierarchy (Ancestors)

Postoperative ComplicationsPathologic ProcessesPathological Conditions, Signs and SymptomsPainNeurologic ManifestationsSigns and Symptoms

Intervention Hierarchy (Ancestors)

AnilidesAmidesOrganic ChemicalsAniline CompoundsAmines

Enrollment

30 participants (actual enrollment reported by the registry).

Study Design

Study Type: interventional
Phase: phase 1
Allocation: RANDOMIZED
Masking: SINGLE
Who Masked: OUTCOMES ASSESSOR
Purpose: PREVENTION
Intervention Model: PARALLEL
Sponsor Type: OTHER
Responsible Party: SPONSOR

Study Record Dates

First Submitted

August 23, 2026

First Posted

August 26, 2026

Study Start

November 2, 2025

Actual (reported)

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American Society of Anesthesiologists (ASA) physical status I , II, III, IV.

Hip surgeries e.g.: Total hip arthroplasty, Hemi-arthroplasty, Fracture neck of femur under spinal anesthesia

You may not qualify if:

Refusal to participate.
Known allergy to local anesthetics.
Coagulopathy or anticoagulant therapy contraindicating regional anesthesia.
Pre-existing neurological deficits in the lower limbs.
Infection at the injection site.
Severe cognitive impairment or inability to assess pain (e.g., advanced dementia).
Failed spinal anesthesia.
Body mass index (BMI) \>40 kg / m²

Contact the study team to confirm eligibility.

Primary Completion

May 2, 2026

Actual (reported)

Study Completion

June 2, 2026

Actual (reported)

Last Updated

August 26, 2026

Record last verified: 2026-08

Source record

Download the complete ClinicalTrials.gov record imported by Syfrah, including fields not shown in this page. The registry may contain a newer revision.

Source: ClinicalTrials.gov.

JSON downloads include source attribution and retrieval details alongside the unchanged original record or the separately normalized values.

Registry identifier: NCT07787442
Data provider: ClinicalTrials.gov
Source updated: 2026-08-26
Normalization version: ctgov-legacy-1

Open registry record

Source retrieved: 2026-10-25 22:24:21 UTC

Locations

EG(1)

Brief Summary

Registry Overview

Trial Relationships

Related Scientific Literature

Study Timeline

Study Start

Primary Completion

Study Completion

First Submitted

First Posted

Conditions

Outcome Measures

Primary Outcomes (1)

Secondary Outcomes (1)

Study Arms (2)

Ultrasound Guided Suprainguinal Fascia Iliaca Compartment Block

Ultrasound Guided Suprainguinal Fascia Iliaca Compartment Block in combination with Sciatic Nerve Bl

Interventions

Eligibility Criteria

You may qualify if:

Sponsors & Collaborators

Study Sites (1)

MeSH Terms

Conditions

Interventions

Condition Hierarchy (Ancestors)

Intervention Hierarchy (Ancestors)

Enrollment

Study Design

Study Record Dates

You may not qualify if:

Source record

Locations