Health Condition 1: O00-O08- Pregnancy with abortive outcome
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1.American society of anesthesiologist physical status grade I, grade II 2.Patient undergoing laparoscopic sterilization
Exclusion criteria
Exclusion criteria: 1.Patient refusal 2.Patients with severe cardiovascular, respiratory, renal, or hepatic diseases 3.known allergies or hypersensitivity to dexmedetomidine, remifentanil 4.Severe Obesity - BMI 35-40 5.History of substance abuse or opioid dependency
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| to compare the intra operative hemodynamic parameters between dexmedetomidine and remifentanil group undergoing laparoscopic sterilizationTimepoint: 0-60 minutes | — |
Secondary
| Measure | Time frame |
|---|---|
| To compare the recovery profile between dexmedetomidine and remifentanil group using modified Aldrete score.Timepoint: starting from immediate post surgery and every 15 minutes till 30 minutes;To compare the immediate post operative painTimepoint: Duration of post operative pain (dexmedetomidine/remifentanil)in minutes | — |
Countries
India
Contacts
SRM medical college and research centre