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NCT Number: NCT06663449

Comparison of ESP Block and STAP Plane Block

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.

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Key information

Age range

18 year–75 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Kocaeli University

Kocaeli, Turkey (Türkiye)

Location contact

Sevim Cesur, MD

CONTACT

+902623038248

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Patients who will undergo laparoscopic cholecystectomy:
  • 18-75 years old
  • ASA I-II-III patients

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

Treatment and study plan

Subcostal Transversus Abdominis Plane Block

Procedure

subcostal transversus abdominis plane block will be performed using 20 mL of 0.25 bupivacaine

Erector Spinae Plane Block

Procedure

erector spinae plane block will be performed using 20 mL of 0.25 bupivacaine

Primary outcomes

  1. NRS Scores

    Time frame: 1 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)

  2. Morphine consumption

    Time frame: 1 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)

Study contacts

Contact information is provided by the study sponsor or research team.

sevim Cesur Okan

CONTACT

[email protected]

0 541 911 41 00

Sponsors and collaborators

Lead sponsor

Kocaeli University

Other

Registry information

Official study title

Comparison of ESP Block and STAP Plane Block in Laparoscopic Cholecystectomy Surgery

Important dates

Study start
2024
Primary completion
2025
Study completion
2025
First posted
Oct 29, 2024
Registry last updated
Dec 5, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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