Health Condition 1: O- Medical and Surgical
Conditions
Interventions
Intervention1: Low Pressure pneumoperitoneum: The total cohort of the study, after obtaining written informed consent, will be randomly assigned to either of the groups (LPP defined as those in whom
Sponsors
PGIMER Chandigarh Adminitration
Eligibility
Inclusion criteria
Inclusion criteria: 1. All patients with symptomatic GSD with chronic cholecystitis undergoing elective laparoscopic cholecystectomy 2. Age: 18years- 65 years
Exclusion criteria
Exclusion criteria: 1. Patients not giving consent for undergoing study 2. Patients with other preoperative causes of shoulder pain like bursitis, rheumatoid arthritis, tendinitis and other musculoskeletal conditions 3. Patients with CAD, COPD, Asthma, previous malignancy, jaundice or any other co-morbidity 4. Patients who have underwent any abdominal surgery previously 5. BMI 29.9 6. Patients on chronic analgesic use or patients with history of addiction to alcohol 7. Patients with significant portal hypertension, uncorrectable coagulopathies, cirrhosis and generalized peritonitis 8. Pregnant patients
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Incidence & intensity of post-operative pain & analgesic requirement in LPP group & SPP groupTimepoint: 6hrs 12hrs 24 hrs | — |
Secondary
| Measure | Time frame |
|---|---|
| surgical field visualizationTimepoint: At end of surgery;duration of hospital stay & time taken for return to workTimepoint: Up to 30 days after surgery;duration of procedureTimepoint: At end of surgery;Effect of pneumoperitoneum on Intra-operative physiologyTimepoint: i. At insufflation of pneumoperitoneum ii. 30 minutes after insufflation iii. Just before reversal of general anaesthesia;incidence of intra-operative complicationsTimepoint: At end of surgery | — |
Countries
India
Contacts
Public ContactDr Vishesh Gupta
Post Graduate Institute of Medical Education and Research, Chandigarh
Outcome results
None listed