About this trial
The Goal of this clinical trial is to determine the advantages of using Peripheral Nerve Block by injecting drugs under the skin on both sides of the abdomen in the upper abdominal area in patients undergoing laparoscopic Cholecystectomy. Study participants will be divided into 2 groups, namely group P1 receiving Modified Thoracoabdominal Perichondrial Approach (M-TAPA) block anesthesia after laparoscopic cholecystectomy and group P2 only receiving intravenous opioids postoperatively. Peripheral nerve blocks on both sides of the upper abdomen are expected to be able to prolong the duration of pain relief, reduce the pain scale, and the total dose of pain medication needed postoperatively. The injection of this peripheral nerve block drug will be carried out by an anesthesiologist. Researchers will continue to anticipate the occurrence of side effects that can occur with strict monitoring and emergency care standards. This study will last up to 24 hours after surgery.
The main question it aims to answer is:
To prove that the amount of postoperative intravenous opioid consumption with M-TAPA block is lower than the control group.
Eligibility criteria
Qualifiers
Patient 18-65 yeasr old
IMT 17.5-30 kg/m2
Patient with ASA I-II
Disqualifiers
Patient Refusal
Local Infection
Chronic Analgesia drug user
Trial design
Treatments tested in this trial
- Modified Thorachoabdominal Nerve Block Perichondrial Approach(M-TAPA
- Opioid Intravena