Modified Thoracoabdominal Plane Block and Rectus Block Combination

The aim of our study was to investigate the effect of the combination of Modified thoracoabdominal plane block (M-TAPA) and rectus sheath block with local infiltration analgesia on postoperative pain scores and opioid use.

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Key information

Conditions

Visual Analogue Scale

Age range

18 year–65 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

Over 18 years old
ASA1-2
Laparoscopic cholecystectomy cases

Exclusion criteria

Bleeding disorders
Anticoagulant use
Patients with previous nerve damage
Lack of patient consent
Patients with liver and kidney failure
Patients allergic to local anesthetics used
Patients with BMI > 35

Treatment and study plan

regional anestesia

Procedure

Modified thoracoabdominal plane block (M-TAPA) and rectus sheath block with local infiltration analgesia

Primary outcomes

visual analogue scale

Time frame: 4 month

Pain score measured using a 0-10 scale, where 0 = no pain and 10 = worst imaginable pain. Higher scores indicate worse pain.

Study contacts

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

ALİ HÜSEYİN DEMİR

CONTACT

[email protected]

+905062958099

Sponsors and collaborators

Lead sponsor

Haseki Training and Research Hospital

Other

Registry information

Official study title

Comparison of Pain Between Modified Thoracoabdominal Plane Block and Rectus Block Combination and Intraperitoneal Local Infiltration Analgesia

Important dates

Study start: 2025
Primary completion: 2025
Study completion: 2025
First posted: Apr 13, 2025
Registry last updated: Apr 17, 2025

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

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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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