Clinical study of propofol and dexmedetomidine for hypotensive anaesthesia.
Phase 3
Completed
- Conditions
- Health Condition 1: null- elective functional endoscopic sinus surgery
- Registration Number
- CTRI/2018/07/014746
- Lead Sponsor
- Department of anaesthesia Faridkot
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 80
Inclusion Criteria
aged 18 to 50 years
ASA grade 1 and 2 patient
elective surgery
Exclusion Criteria
patient refusal
h/0 anaphylaxis to any of the study drug
uncontrolled hypertension
coagulation disorder
ASA grade 3 and 4
pregnant patient
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method blood loss during surgery. <br/ ><br>quality of surgical field. <br/ ><br>haemodynamic changesTimepoint: blood loss during surgery measured during 2-2.5 hour surgery <br/ ><br>quality of surgical field during operative intervention inside sinuses i.e. 1 hour. <br/ ><br>haemodynamic changes during 2- 2.5 hours surgery.
- Secondary Outcome Measures
Name Time Method haemodynamic changesTimepoint: surgery duration