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Clinical Trials in Egypt / NCT07367568
Recruiting Not applicable

Costotransverse Foramen Block With Erector Spinae Plane Block in Modified Radical Mastectomy

NCT07367568 · tracked via the Priya Life Science Egypt tracker
Sponsor
National Cancer Institute, Egypt
Phase
Not applicable
Started
2026-01-24
Last updated
2026-01-27

Condition(s) studied

Costotransverse Foramen BlockErector Spinae Plane BlockModified Radical Mastectomy

Investigational drug(s) / intervention(s)

Costotransverse foramen blockErector spinae plane block

Costotransverse foramen block: Patients will receive an ipsilateral ultrasound-guided costotransverse foramen block with injection of 20 ml bupivacaine 0.25%.

Erector spinae plane block: Patients will receive an ipsilateral ultrasound-guided erector spinae plane block with injection of 20 ml bupivacaine 0.25%.

Study summary

This study aims to compare the costotransverse foramen block with erector spinae plane block in modified radical mastectomy.

Eligibility

Sex
FEMALE
Min age
18 Years
Max age
65 Years
Healthy volunteers
No
Inclusion Criteria: * Adult females \> 18 years and ≤ 65 years old. * American Society of Anesthesiologists (ASA) physical status П-III. * Body mass index (BMI) 18-35 kg/m2. * Scheduled for modified radical mastectomy. Exclusion Criteria: * Known allergy or hypersensitivity to local anesthetic agents. * Active infection at the injection site (e.g., cellulitis, abscess). * Coagulopathy or ongoing anticoagulant/antiplatelet therapy \[International Normalized Ratio (INR) \> 1.5 or platelet count \< 100,000/µL\]. * Severe respiratory, cardiac, hepatic, or renal disease. * Morbid obesity. * Severe cognitive impairment or uncooperative behavior that could interfere with block placement.

Primary outcome measure(s)

  • Total morphine consumption — 24 hours postoperatively
    If the numeric rating scale (NRS) is ≥ 4, an IV morphine dose (3 mg) will be provided Paracetamol 1 gm and ketorolac 30 mg will be administered every 8 hours postoperatively.

Trial sites (1)

FacilityCityRegionStatus
Cairo University Cairo Egypt Recruiting

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Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07367568 on ClinicalTrials.gov ↗ ← All trials in Egypt