To compare the analgesic efficacy of Ultrasound guided injection on back with infiltration on port site in laparoscopic cholecystectomy.
Not Applicable
Completed
- Conditions
- Health Condition 1: K819- Cholecystitis, unspecified
- Registration Number
- CTRI/2020/07/026320
- Lead Sponsor
- AIIMS Raipur
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 60
Inclusion Criteria
1.BMI (18.5-29.9 kg/m2)
2.ASA 1 or 2
Exclusion Criteria
1.Patientââ?¬•s refusal
2.Age <18yrs and >65yrs
3.Inability to properly describe post-operative pain to investigators (language-barriers, neuropsychiatric disorders)
4.Patients having
BMI >30kg/m�²
5.Infection at the injection site
6.Patients with coagulopathy
7.Patients having study drug allergy
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Duration and quality (post-operative VAS Score) of analgesia (time to first rescue analgesia after administration of block)Timepoint: 24 hours
- Secondary Outcome Measures
Name Time Method Intraoperative Fentanyl requirement, total analgesic consumption in 24 hrs after surgery and adverse effects.Timepoint: 24 hours