A comparitive study of efficacy of two different drug combination in reducing adverse events due to the process of insertion of endotracheal tube into the larynx in hypertensive patient
Phase 4
- Conditions
- Health Condition 1: I10- Essential (primary) hypertensionHealth Condition 2: I10- Essential (primary) hypertensionHealth Condition 3: I10- Essential (primary) hypertension
- Registration Number
- CTRI/2021/10/037562
- Lead Sponsor
- vijaynagar institute of medical sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1.ASA physical status II
2.Patients with normal ( modified Mallampatti class I or II )
Exclusion Criteria
1.refusal by patients for the procedure
2.ASA physical status 3 and 4
3.uncontrolled hypertension ( >160/90mmhg)
4.patient with the history of hypersensitivity to inj propofol and inj etomidate
5.Anticipated difficult airway
6.patient with cardiovascular diseases other than hypertension, epilepsy, renal, hepatic disease
7.Brochial asthma and COPD
8.presence of known primary or secondary adrenal insufficiency or on steroid medication
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method