The Additive Analgesic Effects of Transversus Abdominis Plane Block in Abdominoplasty Under Spinal Anaesthesia: A Randomized Controlled Study
Status: Completed
Location: See location...
Intervention Type: Drug
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY
The primary outcome is the time to first request of opioid analgesia. The secondary outcomes are intraoperative analgesic needs, incidence of conversion to general anaesthesia, the total opioid dose in 24 hours, Visual analogue scale (VAS) scores at 2, 4, 6, 12, and 24 hours postoperatively, and the incidence of postoperative side effects (nausea, vomiting, hypotension, bradycardia, and pruritic).
Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 65
Healthy Volunteers: f
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• American Society of Anaesthesiologists physical status grade I and grade II.
• Age \> 18 years and less than 65 years.
• Both sexes.
Locations
Other Locations
Egypt
Egyptian liver hospital
Al Mansurah
Time Frame
Start Date: 2024-05-28
Completion Date: 2025-04-01
Participants
Target number of participants: 66
Treatments
Experimental: Spinal anaesthesia group (S)
patient in S group They will receive 20 mg of 0.5% hyperbaric bupivacaine plus 25 microgram fentanyl.
Experimental: oblique Subcostal TAP block and spinal anaesthesia group (OSTAP)
Patients in (OSTAP) groups had spinal anesthesia administered with 20 mg of 0.5% hyperbaric bupivacaine and 25 mcg of fentanyl. Immediately after giving spinal anesthesia, individuals in the OSTAP group received 35 ml of 0.25% isobaric bupivacaine on each side.
Related Therapeutic Areas
Sponsors
Leads: Helwan University