Not yet recruiting NCT07631416

Lumbar Erector Spinae Plane Block Versus Fascia Iliaca Plane Block in Hip Surgeries as Postoperative Analgesia

Phase IV Interventional Post op Pain in Hip Surgeries

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied: The protocol lists: 0.25% bupivacaine.
Who it may be relevant to: Registry conditions: Post op Pain in Hip Surgeries. Basic parameters: 18 years — 90 years · All.
What needs checking: Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place: Egypt
Next step: Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

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Overview

Lumbar Erector Spinae Plane Block Versus Fascia Iliaca Plane Block in Hip Surgeries as Postoperative Analgesia The aim of this study is to compare the analgesic efficacy of lumbar ElectroSpine Plane Block and Fascia Iliaca Plane Block in patients undergoing hip surgery under spinal anesthesia.

Detailed description

Primary outcome:

• Follow up postoprative pain.

Secondary outcome:

• Requirment of analgesic drugs either (opoid or non opoid) postoprative.

Interventions

Drug 0.25% bupivacaine
Lumbar Erector Spinae Plane Block Versus Fascia Iliaca Plane Block in Hip Surgeries as Postoperative Analgesia

Primary outcome measures

follow up postoperative pain by Visual Analogue Scale (VAS)score [Time frame: follow up postoperative pain in 24 hours]

Secondary outcome measures (1)

Requirment of analgesic drugs either (opoid or non opoid) postoprative by Viscual Analogue Scale (VAS) Score [Time frame: Requirment of analgesic drugs either (opoid or non opoid) postoprative. in 24hours]

Eligibility criteria

Inclusion criteria

• Age between ≥ 18 years

Both sexes.
American Society of Anesthesiologists (ASA) Physical Status I-III
Undergoing elective unilateral hip surgeries under spinal anesthesia
Patients with body mass index (BMI) < 35 kg/m²

Exclusion criteria

• Patient refusal

Known allergy to local anesthetics
Infection at the site of block
Coagulopathy or bleeding disorders
Cognitive impairment affecting pain assessment
Chronic opioid use
Neuromuscular disorders as patients with stroke.

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: Yes

Study design

Allocation: Randomized
Model: Crossover
Masking: Triple blind
Primary purpose: Treatment

Study locations

Egypt · 1 center

sohag University — Sohag

Identifiers

NCT: NCT07631416 · Erector Spinae Plane Block

Primary sources (government registries)

ClinicalTrials.gov (US NIH)

View this study on ClinicalTrials.gov ↗