Comparing pain relief methods for breast cancer 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 study aims to evaluate the effectiveness of two different analgesic techniques, the Erector Spinae Plane block and the mid-point transverse process to pleura block, in patients undergoing modified radical mastectomy for breast cancer. Participants will be randomly assigned to one of the two groups, where they will receive ultrasound-guided injections of bupivacaine to assess pain relief post-surgery. The study will monitor the efficacy of these blocks in managing postoperative pain, which is crucial for recovery and patient comfort.

Why it matters

Who can join: the full rules

Inclusion Criteria:

* ASA I-II.
* Undergoing modified radical mastectomy surgery.
* Body mass index (BMI) from 18.5 to 30 kg/m2

Exclusion Criteria:

* Patient refusal.
* Known allergy to local anesthetics.
* Bleeding disorders; platelets count \<50,000 , prothrombin concentration \< 60% or any coagulopathy disorder.
* Use of any anti-coagulants.
* Inability to provide informed consent.
* ASA III-IV.
* Neurological disorders.
* Patient with psychiatric disorders

Where it's running

• National cancer institute, Cairo University
  Cairo, Egypt Recruiting

Study contacts

• Study coordinator: mahmoud Saad Mahmoud Mohamed Mohamed, Msc
• Email: doc.mahmoudsaad@gmail.com
• Phone: +201094555375

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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.