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Clinical Trials/NCT07311902
NCT07311902
Recruiting
Not Applicable

Comparison of Patient Satisfaction Survey and Pain Follow-up in Patients Who Underwent M-Tapa Block and Transversus Abdominal Plane Block for Postoperative Analgesia in Unilateral Open Inguinal Hernia Repair Surgery

Erzurum Regional Training & Research Hospital1 site in 1 country60 target enrollmentStarted: November 1, 2024Last updated:

Overview

Phase
Not Applicable
Status
Recruiting
Sponsor
Erzurum Regional Training & Research Hospital
Enrollment
60
Locations
1
Primary Endpoint
pain score

Overview

Brief Summary

Patients will be called to the operating room one hour before surgery and no premedication will be applied before coming to the operating room. Patients in both groups who are taken to the block room will be administered 1-2 mg iv midazolam for sedation. M TAPA block will be applied for the surgical procedure. After aseptic conditions are provided, the high-frequency linear US probe will be covered with a sterile sheath. The US probe will be placed in the saggital plane at the costochondral angle where the midclavicular line intersects the costal cartilage. 5 ml of saline will be injected using the in-plane technique using a 22G 100 mm block needle and the block location will be verified. After the block location is verified, a total of 20 ml of 0.25% bupivacaine will be injected unilaterally and the procedure will be terminated. After aseptic conditions are provided, the high-frequency linear US probe will be covered with a sterile sheath. In TAP block, the block needle will be advanced to the fascial plane between the internal oblique and transversus abdominis muscles with the in-plane technique and the procedure will be completed by injecting 5 ml 20 ml 0.25% bupivacaine unilaterally. The same analgesia protocol will be applied to both groups intraoperatively and postoperatively, and a survey will be conducted on the patients at the 24th hour postoperatively.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Other
Masking
Double (Care Provider, Outcomes Assessor)

Eligibility Criteria

Ages
18 Years to 65 Years (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • Planning for elective unilateral open inguinal hernia repair surgery
  • ASA I-II status
  • Being between 18 and 65 years of age

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

pain score

Time Frame: The primary aim of our study was to compare VAS scores at 1, 2, 4, 8, 12, and 24 hours postoperatively and to evaluate the level of comfort.

Patients' pain scores will be evaluated

Secondary Outcomes

  • The QoR-15 Patient Questionnaire, a 40-question global recovery rating system with a Turkish variant(24 hours following surgery.)

Investigators

Sponsor
Erzurum Regional Training & Research Hospital
Sponsor Class
Other Gov
Responsible Party
Principal Investigator
Principal Investigator

Omer Doymus

assistant professor

Erzurum Regional Training & Research Hospital

Study Sites (1)

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