Comparing pain relief methods after cesarean sections

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 study evaluates the effectiveness of different nerve blocks, specifically Erector Spinae and Quadratus Lumborum, as well as Intrathecal Morphine, in managing postoperative pain following cesarean sections. The aim is to determine which method provides the best analgesic relief for patients undergoing elective cesarean deliveries. Participants will be monitored for pain levels and overall recovery outcomes to assess the efficacy of each intervention.

Why it matters

Who can join: the full rules

Inclusion Criteria:

* 18-40 years old
* more or equal 37 weeks of gestation
* ASA 1,2
* Elective cesarean delivery

Exclusion Criteria:

* Patient refusal
* inability to cooperate with or understand the study
* local infection.
* bleeding disorder
* known anaphylaxis to any drug used in the trial
* ASA physical status more than 2
* emergency operations
* chronic opioid use (opioid use in the past 3 months)
* Neurologic deficit or disorder
* contraindication to regional anesthesia.

Where it's running

• Mahmoud Mamdouh Ekram
  Asyut, Manfalout, Egypt Recruiting

Study contacts

• Study coordinator: Ghada Abo Elfadl, MD
• Email: ghadafadl77@gmail.com
• Phone: 01005802086

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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.