Pain Management, Mtapa Block, TAP Block
Conditions
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.
Interventions
PROCEDURETAP Block Group
20 ml of 0.25% bupivacaine
PROCEDUREM TAPA block
20 ml of 0.25% bupivacaine
Sponsors
Erzurum Regional Training & Research Hospital
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
OTHER
Masking
DOUBLE (Caregiver, Outcomes Assessor)
Eligibility
Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No
Exclusion criteria
* History of bleeding diathesis * Allergy or sensitivity to local anesthetics and opioids * Infection in the area where the block will be applied * Alcohol or drug addiction * Patients with a BMI \> 30 * Suspected pregnancy * Women in pregnancy or lactation * Patients with allergies to study drugs * Patient refusal * Use of anticoagulant agents Inclusion Criteria: * Planning for elective unilateral open inguinal hernia repair surgery * ASA I-II status * Being between 18 and 65 years of age
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| pain score | 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
| Measure | Time frame | Description |
|---|---|---|
| The QoR-15 Patient Questionnaire, a 40-question global recovery rating system with a Turkish variant | 24 hours following surgery. | To compare patient satisfaction survey and pain monitoring in patients who underwent M-Tapa Block and Transversus Abdominal Plane block for postoperative analgesia in unilateral open inguinal hernia repair surgery and to suggest a more effective method. |
Countries
Turkey (Türkiye)
Contacts
Primary Contactomer doymus
Outcome results
None listed