To compare the effectiveness between inj vitamin C and inj lignocaine regarding pain due to inj propofol
Phase 3
- Conditions
- Health Condition 1: R52- Pain, unspecified
- Registration Number
- CTRI/2020/12/029797
- Lead Sponsor
- Bhu medical and surgical
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1..patient belonging to ASA physical status 1 and 2.
2.Hemodynamically stable.
Exclusion Criteria
1.Patients refusal
2.patients with allergy to PROPOFOL, lignocaine and vitamin C.
3.patient with cardiac conduction defect.
4.patient with congenital heart disease..
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Pain grading scale during and after the surgeryTimepoint: Preoperative at the end of surgery before extuabtion and 6 hr postoperative...
- Secondary Outcome Measures
Name Time Method ATimepoint: NA