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Comparison of Serratus Posterior Superior Intercostal Plane Block and Erector Spinae Plane Block for Postoperative Analgesia in Unilateral Breast Surgery: A Prospective, Randomized, Assessor-Blinded Trial

Status: Recruiting
Location: See location...
Intervention Type: Procedure
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

This prospective, randomized, assessor-blinded trial compares serratus posterior superior intercostal plane block (SPSIPB) and erector spinae plane block (ESPB) for postoperative analgesia in unilateral breast surgery. 54 patients will be randomized to receive either SPSIPB or ESPB before general anesthesia. The primary outcome is postoperative pain scores within the first 24 hours. The secondary outcome is opioid consumption.

Eligibility
Participation Requirements
Sex: Female
Minimum Age: 18
Maximum Age: 65
Healthy Volunteers: f
View:

• Female patients aged 18-65 years

• ASA physical status I-III

• Body mass index (BMI) between 18 and 35 kg/m²

• Scheduled for elective unilateral breast surgery (mastectomy with or without sentinel lymph node biopsy)

• Ability to understand and provide written informed consent

Locations
Other Locations
Turkey
University of Health Sciences Kocaeli City Hospital
RECRUITING
İzmit
Contact Information
Primary
Engin Çetin, M.D.
Doccetin52@gmail.com
5321206004
Backup
Engin Çetin, M.D
Doccetin52@gmail.com
5321206004
Time Frame
Start Date: 2026-05-01
Estimated Completion Date: 2026-09-01
Participants
Target number of participants: 54
Treatments
Active_comparator: SPSIP Block
Participants will receive an ultrasound-guided serratus posterior superior intercostal plane block (SPSIPB) with 30 mL of 0.25% bupivacaine prior to induction of general anesthesia.
Active_comparator: ESPB Block
Participants will receive an ultrasound-guided erector spinae plane block (ESPB) with 30 mL of 0.25% bupivacaine prior to induction of general anesthesia.
Related Therapeutic Areas
Sponsors
Leads: Engin Çetin

This content was sourced from clinicaltrials.gov

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