Last Verified: | May/31/2018 |
First Submitted: | November/29/2016 |
Estimated Enrollment Submitted: | December/1/2016 |
First Posted: | December/5/2016 |
Last Update Submitted: | June/12/2018 |
Last Update Posted: | June/13/2018 |
Actual Study Start Date: | November/30/2016 |
Estimated Primary Completion Date: | May/17/2018 |
Estimated Study Completion Date: | June/12/2018 |
Study Type: | Interventional |
Allocation: | Randomized |
Primary Purpose: | Health Services Research |
Masking: | Double (Investigator, Outcomes Assessor) |
Arm | Intervention/treatment |
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Active Comparator: TAP block group (Group T) At the end of the operation, patients in Group T in the supine position will have a USI probe placed at the middle point between the costal edge and iliac crest (within the Petit triangle) after necessary antiseptic conditions are ensured. Then after the abdominal muscle layers are observed, the needle tip will be advanced through the muscle layers and pass the fascia, feeling the fascial click, monitored by USI in controlled fashion. After feeling the second click (passing the internal oblique muscle fascia), a test dose of 0.5-1 ml saline will be administered to determine the localization of the needle tip. Then noting the location, with frequent aspiration local anesthetic agent will be administered to the neurofascial plane for TAP block. | Procedure: TAP block group (Group T) At the end of the operation, patients in Group T in the supine position will have a USI probe placed at the middle point between the costal edge and iliac crest (within the Petit triangle) after necessary antiseptic conditions are ensured. Then after the abdominal muscle layers are observed, the needle (Stimuplex Ultra 22G, 100mm, B.Braun, Germany) tip will be advanced through the muscle layers and pass the fascia, feeling the fascial click, monitored by USI in controlled fashion. After feeling the second click (passing the internal oblique muscle fascia), a test dose of 0.5-1 ml saline will be administered to determine the localization of the needle tip. Then noting the location, with frequent aspiration local anesthetic agent will be administered to the neurofascial plane for TAP block. |
Active Comparator: Group without TAP (Group P) Patients in Group P will have adjuvant added to spinal anesthesia. | Procedure: Group without TAP (Group P) Patients in Group P will have adjuvant added to spinal anesthesia (25 G, Quincke spinal anesthesia needle, Egemen,Turkey). |
Ages Eligible for Study: | 18 Years to 18 Years |
Sexes Eligible for Study: | Male |
Accepts Healthy Volunteers: | Yes |
Criteria: | Inclusion Criteria: 18-45 year old ASA I-II patient group Exclusion Criteria: 1. Contraindications for spinal anesthesia 2. Coagulopathy 3. Known allergy to medications used 4. Infection in the operated area 5. Non-volunteer patient |