Health Condition 1: O- Medical and Surgical
Conditions
Interventions
Intervention1: Double blinded randomised controlled trial: Efficacy of intraperitoneal instillation of 0.25% levo bupivacaine 10ml versus 0.25% Ropivacaine 10ml in hemi diaphragmatic port for post ope
Sponsors
Malepati Chandana
Eligibility
Inclusion criteria
Inclusion criteria: Patients posted for elective laparoscopic cholecystectomy Patients of age group 18 to 60 years ASA physical status I and II
Exclusion criteria
Exclusion criteria: Patients with H/O drug allergies Patients with H/O bleeding disorders
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Efficacy of two different local anaesthetics Levobupivaine & Ropivacaine when given as intraperitoneal instillation following laparoscopic cholecystectomy in terms ofTimepoint: Duration of post operative pain relief 24 hour post operative analgesic requirement | — |
Secondary
| Measure | Time frame |
|---|---|
| To compare the hemodynamic changes following intraperitoneal instillation of levo bupivacaine & ropivacaine following laparoscopic cholecystectomyTimepoint: Within 18 months of duration | — |
Countries
India
Contacts
Public ContactMalepati Chandana
Sri Venkateswaraa medical college Hospital and research centre, Puducherry
Outcome results
None listed