Ankara Etlik City Hospital
Ankara, 06010, Turkey (Türkiye)
NCT Number: NCT06995404
Although laparoscopic techniques are considered minimally invasive surgical procedures with lower perioperative pain scores compared to open surgeries, they are still associated with significant levels of pain. This study aims to investigate the analgesic effectiveness of two routinely performed regional analgesic techniques in our clinic-ultrasound-guided classic bilateral TAP block and ultrasound-guided bilateral M-TAPA block-in patients undergoing laparoscopic gyneco-oncologic surgery (LGOS), as well as their effects on intraoperative opioid consumption.
Trial opening soon.
Get Notified18 year–80 year
Female
Interventional
Not applicable
Ankara, 06010, Turkey (Türkiye)
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Female patients aged between 18 and 80 years, classified as ASA physical status I to III, undergoing laparoscopic gynecologic surgery under general anesthesia -
Exclusion criteria
Coagulopathy
Neuropathy
Chronic analgesic therapy
Severe cardiopulmonary disease
Uncontrolled diabetes mellitus (HbA1c > 8%)
Severe renal or hepatic failure
Pregnancy or lactation
Body mass index (BMI) greater than 35 kg/m²
Local infection at the injection site
Inability to comprehend pain scores or cooperate (e.g., Alzheimer's disease, mental retardation)
Allergy to local anesthetic agents
Refusal to participate in the study
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Patients in the TAP group will receive a bilateral Transversus Abdominis Plane (TAP) block under ultrasound guidance prior to surgery after general anaesthesia, with the local anesthetic administered between the internal oblique and transversus abdominis muscles. A total of 40 mL of 0.25% bupivacaine will be used for the procedure.
Patients in the M-TAPA group will receive a bilateral Thoracoabdominal Nerve Block through Perichondrial Approach (M-TAPA) under ultrasound guidance prior to surgery after general anaesthesia. A total of 40 mL of 0.25% bupivacaine will be used for the procedure.
Time frame: during surgery
Time frame: postoperative first day
VAS is an eleven-scale pain score scored from 0 to 10, with vas 0 being no pain and vas 10 being maximum pain.
Contact information is provided by the study sponsor or research team.
Ankara Etlik City Hospital
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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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