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Comparison of ESP Block and STAP Plane Block

Not Applicable
Not yet recruiting
Conditions
Postoperative Pain
Registration Number
NCT06663449
Lead Sponsor
Kocaeli University
Brief Summary

In order to effectively manage postoperative analgesia in patients planned to undergo elective laparoscopic cholecystectomy, patients will be divided into 2 (two) groups and informed consent forms will be obtained after the necessary information is provided so that both groups can be included in the study. In the group planned to undergo erector spinae plane block, erector spinae plane block will be performed after monitoring and sedation in the operating room block unit before being taken to the surgical table preoperatively and postoperative PCA analgesia will be applied. In patients who will undergo subcostal transversus abdominis plane block, subcostal tap block will be performed after monitoring and sedation in the operating room block unit before being taken to the surgical table preoperatively and postoperative PCA analgesia will be applied. The patients' perioperative pain will be monitored with NOL (nociception level) monitor. Remifentanil dose will be adjusted to keep the NOL level between 10 and 25. After the patients are followed up for 24 hours postoperatively, their additional analgesia needs and amounts during this process will be compared. In this way, it is aimed to show that the analgesic method can be used effectively in the follow-up of pain management by comparing the Erector Spina Plane block and the Subcostal Transversus Abdominis Plane block as an effective analgesic application in laparoscopic cholecystectomy operations.

Detailed Description

Not available

Recruitment & Eligibility

Status
NOT_YET_RECRUITING
Sex
All
Target Recruitment
68
Inclusion Criteria
  • Patients who will undergo laparoscopic cholecystectomy:
  • 18-75 years old
  • ASA I-II-III patients
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Exclusion Criteria
  • Use of anticoagulant drugs
  • Known allergy to drugs to be used
  • Infection in the area where the block will be performed
  • Patient's reluctance
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Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Primary Outcome Measures
NameTimeMethod
NRS Scores1 hours after surgery(T1), 3 hours after surgery (T2), 6 hours after surgery (T3), 12 hours after surgery (T4) and 24 hours after surgery(T5)

NRS scores of the patients after the surgery (0=no pain, 10=worst pain imaginable)

Morphine consumption1 hours after surgery(T1), 3 hours after surgery (T2), 6 hours after surgery (T3), 12 hours after surgery (T4) and 24 hours after surgery(T5)

Amount of morphine consumption (mg)

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Kocaeli University

🇹🇷

Kocaeli, Turkey

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