Health Condition 1: K829- Disease of gallbladder, unspecified Health Condition 2: N448- Other noninflammatory disorders ofthe testis
Conditions
Interventions
Intervention1: GROUP PRPOFOL: In group P,In the group P , propofol maintenance shall be done with infusion pump at a rate of 8-10 mg/kg/hr with a target BIS of 40-60.
Control Intervention1: GROUP SEVO
Sponsors
Department of anesthesia AIIMS BBSR
Eligibility
Inclusion criteria
Inclusion criteria: After obtaining institutional ethic committee approval , this prospective randomised clinical trial shall be done in all pediatric patients under age group of 2 to 15 year posted for laparoscopic surgery with trendelenburg position.
Exclusion criteria
Exclusion criteria: Patients with preexisting glaucoma, chronic obstructive pulmonary disease, raised intracranial pressure will be excluded from the study.
Design outcomes
Secondary
| Measure | Time frame |
|---|---|
| 2) Post Operative emergence times and delirium scores differences in Between two Groups. Timepoint: postoperative | — |
Primary
| Measure | Time frame |
|---|---|
| 1) To Compare The Difference In ONSD After Creation Of Pneumoperitoneum in between the two groups of sevoflurane and propofol. Timepoint: intraoperative- before creation of pneumoperitoneum and after creation of pneumoperitoneum | — |
Countries
India
Contacts
Public ContactNitasha Mishra
Department of Anaesthesiology, AIIMS, Bhubaneswar
Outcome results
None listed