A clinical trial to study the comparative effect of two doses of nebulised dexmedetomidine on vital parameters ( Blood pressure and heart Rate) during General anaesthesia in adults
Phase 4
- Conditions
- Health Condition 1: O- Medical and Surgical
- Registration Number
- CTRI/2022/04/042063
- Lead Sponsor
- Jyoti kanwat
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1 The patients of either sex in the age group of 18 to 60 years with American Society of Anesthesiologists Physical Status I and II undergoing elective surgery under general anaesthesia.
Exclusion Criteria
1Patients who are not giving consent
2Patients with ASA III and ASA IV
3Patients with anticipated difficult intubation.
4Pregnant patient
5Patient with body mass index > 30 kg/m2
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To compare the two doses of nebulised dexmedetomidine as premedication on hemodynamic response to laryngoscopy and intubation reflex.Timepoint: 24 weeks
- Secondary Outcome Measures
Name Time Method 1.To measure post nebulization sedation <br/ ><br>2.To determine the post-op sore throat <br/ ><br>Timepoint: 3 months