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NCT05920265 Clinical Trial

Quadratus Lumborum Plain Block Versus Fascia Iliac Block

Post Operative Pain Clinical Trial

Official title:
Quadratus Lumborum Plain Block Versus Fascia Iliac Block in Hip Fracture

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT05920265
Other study ID # 16:2021
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date February 1, 2021
Est. completion date September 1, 2022

Study information
Verified date June 2023
Source Minia University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

evaluation the efficacy of Quadratus Lumborum plain Block Versus Fascia Iliac Block for postoperative pain after hip surgery

Recruitment information / eligibility
Status Completed
Enrollment 60
Est. completion date September 1, 2022
Est. primary completion date June 15, 2022
Accepts healthy volunteers No
Gender All
Age group 18 Years to 70 Years
Eligibility Inclusion Criteria: - 18-70 years - fracture hip Exclusion Criteria: - patients refuse - mental problem patient with any coagulation deficiency or bleeding problems patient with allergy to investigated medications,

Study Design

Related Conditions & MeSH terms

Intervention

Procedure:
• Quadratus Lumborum plain Block
ultrasound guided Quadratus Lumborum plain Block using 0.5 ml/kg bupivacaine 0.25% .
• fascia iliaca block
ultrasound guided fascia iliaca block using 0.5 ml/kg bupivacaine 0.25%
Diagnostic Test:
• control group
no intervention

Locations
Country Name City State
Egypt Minia University Minya Minia

Sponsors (1)
Lead Sponsor Collaborator
Minia University

Country where clinical trial is conducted

Egypt, 

Outcome
Type Measure Description Time frame Safety issue
Primary analgesic consumption intraoperative and post operative 24 hour
Secondary Visual analogue pain score score 0-10 which mean 0 no pain and 10 the worst pain 24 hour
Secondary first analgesic demand the first time to intake rescue analgesia 24 hour
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