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OpenTrials
Completed

NCT Number: NCT05920265

Quadratus Lumborum Plain Block Versus Fascia Iliac Block

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

Completed

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Key information

Age range

18 year–70 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Minia University

Minya, Minya Governorate, 61511, Egypt

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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,

Treatment and study plan

Quadratus Lumborum plain Block

Procedure

ultrasound guided Quadratus Lumborum plain Block using 0.5 ml/kg bupivacaine 0.25% .

Fascia iliaca block

Procedure

ultrasound guided fascia iliaca block using 0.5 ml/kg bupivacaine 0.25%

Control group

Diagnostic Test

no intervention

Primary outcomes

  1. analgesic consumption

    Time frame: 24 hour

    intraoperative and post operative

Secondary outcomes

  1. Visual analogue pain score

    Time frame: 24 hour

    score 0-10 which mean 0 no pain and 10 the worst pain

  2. first analgesic demand

    Time frame: 24 hour

    the first time to intake rescue analgesia

Sponsors and collaborators

Lead sponsor

Minia University

Other

Registry information

Official study title

Quadratus Lumborum Plain Block Versus Fascia Iliac Block in Hip Fracture

Important dates

Study start
2021
Primary completion
2022
Study completion
2022
First posted
Jun 27, 2023
Registry last updated
Jun 27, 2023

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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