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Clinical Trials in Turkey / NCT06601413
Enrolling by invitation Not applicable

Modified Thoracoabdominal Nerve Block(M-TAPA) in Total Laparoscopic Hysterectomies

NCT06601413 · tracked via the Priya Life Science Turkey tracker
Phase
Not applicable
Started
2024-10-01
Last updated
2024-09-19

Condition(s) studied

Pain,Postoperative

Investigational drug(s) / intervention(s)

M-TAPA BlockTrocar site local anesthetic infiltration

M-TAPA Block: M-TAPA block will administer ultrasound guided (Sonosite, Inc., Bothell, WA, USA) bilaterally by same anesthesiologist (E.E.) who had more than 10 years experience of regional anesthesia, before weaking from general anesthesia after the surgical procedure. A high-frequency (6-13 MHz) linear probe (HFL38) will be used to identify the transversus abdominis, internal oblique, and external oblique muscles on the costochondral angle in the sagittal plane at the 10th costal margin. In the midclavicular line, between the upper fascia of the transversus abdominis muscle and the lower fascia of the costochondral tissue, at the level of the 10th rib, 20 mL of 0.25 percent bupivacaine will be injected (arcus costarum). The same procedure will be followed on the other side.

Trocar site local anesthetic infiltration: At the end of surgery, infiltration analgesia will be applied to all trocar entry sites (4 port entries) by the surgeon with 10 ml of 0.25% bupivacaine (40 mL in total) without waking the patient.

Study summary

The aim of the study is comparing the postoperative effects of ultrasound-guided Modified Perichondrial Approach to Thoracoabdominal Nerves (M-TAPA) block for postoperative pain control after total laparoscopic hysterectomy.

Eligibility

Sex
FEMALE
Min age
18 Years
Max age
65 Years
Healthy volunteers
No
Inclusion Criteria: * Ages 18-65 * Elective cases * ASA I-III functional status * Body mass index (BMI)\<35 * Total laparoscopic hysterectomy planned with general anesthesia * No contraindications for M-TAPA block to be applied * Cases that give written and verbal consent for participation in the study will be included. Exclusion Criteria: * Conversion to open surgery * Development of perioperative complications (due to surgery and/or anesthesia) * Coagulation disorder * Infection at the injection site * Allergy to local anesthesia * Those who used any painkillers in the preoperative 24 hours * Those who did not agree to participate in the study

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Health Sciences University Ankara Turkey (Türkiye)

More Gulhane Training and Research Hospital trials in Turkey

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06601413 on ClinicalTrials.gov ↗ ← All trials in Turkey