Health Condition 1: O- Medical and Surgical
Conditions
Interventions
Intervention1: Ropivacaine: Intraperitoneal and infiltration on the port-site with 0.5% ropivacaine 2mg/kg diluted with normal saline to 50 ml
Control Intervention1: Ropivacaine plus dexmedetomidine
Sponsors
NH Rabindranath Tagore International Institute of Cardiac Sciences
Eligibility
Inclusion criteria
Inclusion criteria: 1. Patients who gave written informed consent 2. ASA Physical Status I, II or III 3. Age 35-60 years 4. Elective laparoscopic hysterectomy under general anaesthesia
Exclusion criteria
Exclusion criteria: Patients who: 1. Refused to sign the consent 2. Had allergic history to any drug 3. Were unable to understand VAS 4. Were drug addicts and psychiatric patients 5. Had genital malignancy 6. Had deep pelvic endometriosis
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| - Comparative pain assessment using VAS score in 2 groups - Time to first rescue analgesia - Total analgesic consumptionTimepoint: 30 min 1 hour 4 hour 8 hour 12 hour 16 hour 24 hours | — |
Secondary
| Measure | Time frame |
|---|---|
| Post op Nause & Vomitting Any other adverse eventTimepoint: 24hour | — |
Countries
India
Contacts
Public ContactKamya Bansal
NH Rabindranath Tagore International Institute of Cardiac Sciences
Outcome results
None listed