Clinical trials

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Condition / disease
Location
Status: Not yet recruiting

SPSIP Block Versus ESP Block for Chronic Pain After Unilateral Breast Surgery

This prospective, randomized, assessor-blinded study will compare serratus posterior superior intercostal plane block and erector spinae plane block in adult female patients undergoing unilateral breast surgery. The primary outcome is chronic postoperative pain at 3 months, assessed using the Brief Pain Inventory-Short Form.

Participants needed: 90
Trial details
Age: 18-65Biological sex: FemaleType: InterventionalSponsor: Engin ÇetinUpdated: Jun 30, 2026Locations: 1
Eligibility criteria

Female patients aged 18-65 years [+4]

Infection at the site of block application [+9]

Status: Recruiting

Serratus vs ESP Block for Postoperative Pain in Unilateral Breast Surgery

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.

Participants needed: 54
Trial details
Age: 18-65Biological sex: FemaleType: InterventionalSponsor: Engin ÇetinUpdated: Jun 23, 2026Locations: 1
Eligibility criteria

Female patients aged 18-65 years [+4]

Infection at the site of block application [+9]

Status: Recruiting

Pneumoperitoneum Pressure and Lung Ultrasound Atelectasis

Elective laparoscopic cholecystectomy may lead to perioperative atelectasis due to pneumoperitoneum-related diaphragmatic elevation and impaired respiratory mechanics. Lung ultrasound (LUS) provides a noninvasive bedside method for evaluating perioperative aeration loss. This prospective randomized controlled study aims to compare the effects of low-pressure (10 mmHg) and standard-pressure (14 mmHg) pneumoperitoneum on perioperative atelectasis assessed by LUS in patients undergoing laparoscopic cholecystectomy under general anesthesia. Changes in LUS scores, respiratory mechanics, oxygenation, and postoperative clinical outcomes will also be evaluated.

Participants needed: 112
Trial details
Age: 18-65Biological sex: AllType: InterventionalSponsor: Engin ÇetinUpdated: Jun 23, 2026Locations: 1
Eligibility criteria

Patients aged between 18 and 65 years [+4]

Chronic pulmonary disease [+9]