Using magnesium sulfate with bupivacaine for pain relief after hip surgery

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This clinical trial evaluates the effectiveness of adding magnesium sulfate to bupivacaine in an ultrasound-guided transmuscular quadratus lumborum block for postoperative pain management in adults undergoing hip arthroplasty. The study aims to determine if magnesium sulfate can reduce pain scores and total opioid consumption compared to a placebo. Participants will receive either the combination of magnesium sulfate and bupivacaine or bupivacaine with saline, followed by monitoring for pain and side effects for 48 hours post-surgery.

Why it matters

Who can join: the full rules

Inclusion Criteria:

* Age ≥ 18 years.
* American Society of Anesthesiology (ASA) class I-III
* Undergoing hip arthroplasty .

Exclusion Criteria:

* Patient refusal.
* Body mass index (BMI) \> 40 Kg/m2.
* Allergy to local anesthetics or magnesium sulphate.
* coexisting coagulopathy.
* Local infection at puncture site.
* Severe renal impairment ( eGFR \< 30 ml/min)

Where it's running

• Faculty of medicine
  Tanta, El-Gharbia, Egypt Recruiting

Study contacts

• Principal investigator: Mostafa Mohammad Abdelsattar Elbagoury, MD — lecturer of anesthesia and surgical ICU and pain medicine
• Study coordinator: Mostafa Mohammad Abdelsattar Elbagoury, MD
• Email: mostafa.elbagoury@med.tanta.edu.eg
• Phone: +201116297741

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How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.