RISS Versus ESP Block in Laparoscopic Cholecystectomy
ConditionPostoperative Pain
Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-75
SponsorFerit Yetik
About this trial
This prospective randomized controlled trial aims to compare the analgesic efficacy and effects on diaphragmatic function of bilateral erector spinae plane (ESP) block and bilateral rhomboid intercostal-subserratus plane (RISS) block in patients undergoing elective laparoscopic cholecystectomy. Postoperative pain scores, opioid consumption, diaphragmatic excursion, pulmonary function, and recovery outcomes will be evaluated.
Eligibility criteria
Qualifiers
Age between 18 and 75 years
ASA physical status I-III
Scheduled for elective laparoscopic cholecystectomy under general anesthesia
Provision of written informed consent
Disqualifiers
Coagulation disorders or anticoagulant therapy
Known allergy to local anesthetics
Infection at the block application site
Pregnancy or lactation
Trial design
Treatments tested in this trial
- Erector Spinae Plane Block
- Rhomboid Intercostal-Subserratus Plane Block
Treatment groups
80 Participants
are divided into 2 treatment groupsSponsors and collaborators
Ferit Yetik
Lead sponsor
Bursa Yuksek Ihtisas Training and Research Hospital
Sponsor institution
Bursa City Hospital
Collaborator
Source ClinicalTrials.gov