Health Condition 1: K811- Chronic cholecystitis Health Condition 2: K804- Calculus of bile duct with cholecystitis Health Condition 3: 3- Administration
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Patients Aged 18 To 85 Years. Patients With American Society of Anesthesiologists (ASA) Physical Status Scores Ranging From 1 To 3. Patients Who Are Given Consent and Willing to Participate in This Study.
Exclusion criteria
Exclusion criteria: Patients Classified as Having an ASA Score of IV Those Falling Outside the Specified Age Range. Individuals With Peptic Ulcers, Severe Hepatic or Renal Failure, Significant Cardiovascular or Pulmonary Conditions. A History of Drug Allergies (Specifically, Propofol, Fentanyl, Rocuronium, Paracetamol, Ibuprofen, And Tramadol). As Well As Cases of Emergency Surgery. Individuals Who Did Not Provide Informed Consent.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The primary objective of this study was to assess and compare the impact of iv ibuprofen and paracetamol on postoperative pain intensity through numeric rating scale .Timepoint: Post operative 1st, 6th, 12th, and 24th hours | — |
Secondary
| Measure | Time frame |
|---|---|
| As secondary objectives, this study assesses tramadol consumption as rescue analgesic, analyzes intraoperative hemodynamic parameters, and the investigates any adverse effects related to study drugs in patients who underwent laparoscopic cholecystectomy surgery.Timepoint: intraoperatively baseline , 5minutes ,10minutes ,30minutes ,60minutes ,90minutes ,120minutes postoperatively 1st hour ,6th hour ,12th hour ,24th hour | — |
Countries
India
Contacts
Institute of Medical Sciences BHU