A study to compare improvement in pain relief when intravenous lignocaine is used in patients undergoing surgery to remove the gall bladder.
Phase 3
- Conditions
- Health Condition 1: null- Patients posted for laparascopic elective cholecystectomy
- Registration Number
- CTRI/2018/01/011486
- Lead Sponsor
- Christian Medical College Vellore
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Open to Recruitment
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
a)Patients undergoing elective cholecystectomy
b)BMI >30
c)ASA I and II
d)Age >18
Exclusion Criteria
a)ASA III and IV
b)allergy to local anaesthetic
c)Seizure disorder
d)Anti-arrhythmic drug intake in the 1 week before surgery
e)Renal/Hepatic Insufficiency
f)Psychiatric disorders
g)Steroid therapy
h)Pregnancy
i)Conversion to laparotomy
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Perioperative AnalgesiaTimepoint: Perioperative Analgesia
- Secondary Outcome Measures
Name Time Method Time to DischargeTimepoint: Time to Discharge;time to pass flatus and initiate feedsTimepoint: time to pass flatus and initiate feeds;Ability to do incentive spirometerTimepoint: 10,30,60,90,120 mins after extubation;Hemodynamic ParametersTimepoint: intubation, insufflation, extubation, post extubation every 30 mins for 2 hours;total muscle relaxant usedTimepoint: intraoperatively;total opioids consumedTimepoint: upto 2 hours fter the surgery