Health Condition 1: N939- Abnormal uterine and vaginal bleeding, unspecified
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Adult females aged between 45 to 65 years undergoing elective total abdominal hysterectomy. American Society of Anaesthesiologist (ASA) physical status I or II.
Exclusion criteria
Exclusion criteria: ASA grade III & IV Patients with a known sensitivity to local anaesthetics. Patients with severe cardiovascular, hepatic, or renal disease. Patients undergoing emergency surgeries. Patients with psychiatric disorders affecting the ability to provide informed consent & interfere with evaluation of pain scores. Patient with allergy at the site of block.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| To compare the duration of postoperative analgesia with 0.2 ropivacaine and dexmedetomidine as adjuvant to 0.2 ropivacaine in Ultrasound guided bilateral quadratus lumborum block in post-operative patients undergoing TAHTimepoint: Assessed for 24 hours after surgery | — |
Secondary
| Measure | Time frame |
|---|---|
| To evaluate the safety & side-effect profile of adding dexmedetomidine to ropivacaine in Quadratus Lumborum block, including monitoring for hypotension, bradycardia, sedation, & any other potential complications.Timepoint: Post operative nausea bradycardia hypotension vomiting will be observed at 0 2 4 6 8 12 & 24 hours | — |
Countries
India
Contacts
Shri balaji institute of medical science Raipur