CTRI/2018/07/015137CompletedPhase 4
Comparative evaluation of dexmedetomidine and clonidine on propofol consumption, haemodynamics and postoperative recovery in laproscopic surgeries: A prospective,double blind, placebo controlled, randomized study.
Apollo Hospitals Bilaspur CG0 sites95 target enrollmentStarted: TBDLast updated:
Trial Snapshot
- Phase
- Phase 4
- Status
- Completed
- Sponsor
- Enrollment
- 95
Study Overview
Brief Summary
No summary available.
Study Design
- Study Type
- Interventional
Eligibility Criteria
Inclusion Criteria
- •1. ASA grade I and II
- •2. Non hypertensive and non diabetic
Exclusion Criteria
- •1. Known allergy to study drug,
- •2. Morbid obesity (body mass index >40),
- •3. Chronic use of opioids ,
- •4. Current treatment with a ß-blocker or calcium channel blocker
- •5. Diabetes and hypertension
- •6. Known asthma or reactive airway disease,
- •7. Hepatic, renal or cardiovascular dysfunction
- •8. Any degree of heart block
- •9. Psychiatric patients
- •10. Pregnant and lactating women
Investigators
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