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NCT05744544 Clinical Trial

Sensory Assessment and Regression Rate of Bilateral External Oblique Intercostal Block and m-TAPA Block

Pain Clinical Trial

Official title:
Sensory Assessment and Regression Rate of Bilateral External Oblique Intercostal Block and m-TAPA Block in Patients Undergoing Laparoscopic Cholecystectomy

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT05744544
Other study ID # DERMATOM55
Secondary ID
Status Completed
Phase
First received
Last updated
Start date May 2, 2023
Est. completion date August 7, 2023

Study information
Verified date June 2024
Source Samsun University
Contact n/a
Is FDA regulated No
Health authority
Study type Observational [Patient Registry]

Clinical Trial Summary

External oblique and m-tapa blocks are routinely performed on patients undergoing laparoscopic cholecystectomy in our clinic. In this study, sensory block and regression rates will be investigated in patients who underwent block.

Description:

External oblique block and m-Tapa blocks may be the key to provide adequate analgesia in patients undergoing abdominal surgery by blocking the abdominal nerves. In this study, the sensory dermatome block area calculation and the regression rate of the blocks will be evaluated in patients who underwent EOIB and m-Tapa.

Recruitment information / eligibility
Status Completed
Enrollment 24
Est. completion date August 7, 2023
Est. primary completion date August 3, 2023
Accepts healthy volunteers
Gender All
Age group 18 Years to 65 Years
Eligibility Inclusion Criteria: - Patients undergoing L/S cholecystectomy Exclusion Criteria: - patients who do not want to participate

Study Design

Related Conditions & MeSH terms

Intervention

Procedure:
• External Oblique Block
Patients will be followed after EOIB which are routinely performed in our clinic.
• m-TAPA block
m-TAPA block

Locations
Country Name City State
Turkey Samsun University Samsun

Sponsors (1)
Lead Sponsor Collaborator
Samsun University

Country where clinical trial is conducted

Turkey, 

References & Publications (2)

Chen Y, Shi K, Xia Y, Zhang X, Papadimos TJ, Xu X, Wang Q. Sensory Assessment and Regression Rate of Bilateral Oblique Subcostal Transversus Abdominis Plane Block in Volunteers. Reg Anesth Pain Med. 2018 Feb;43(2):174-179. doi: 10.1097/AAP.000000000000071 — View Citation

Stoving K, Rothe C, Rosenstock CV, Aasvang EK, Lundstrom LH, Lange KH. Cutaneous Sensory Block Area, Muscle-Relaxing Effect, and Block Duration of the Transversus Abdominis Plane Block: A Randomized, Blinded, and Placebo-Controlled Study in Healthy Volunt — View Citation

Outcome
Type Measure Description Time frame Safety issue
Primary Sensory Assessment on the anterolateral abdominal wall Sensory Assessment will be performed on patients following the block procedure with pinprick test. 24 hours
Primary Regression Rate of the cutaneous block on anterolateral abdominal wall Regression Rate will be performed on patients following the block procedure with pinprick test. 24 hours
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