Effect of propofol-fentanyl, propofol-midazolam and propofol-dexmedetomidine combination on pulse rate, blood pressure and postoperative recovery for endoscopic procedure
Phase 4
Completed
- Conditions
- Health Condition 1: null- ASA grade I or III patient, Non diabetic, Non hypertensive and require Endoscopic retrograde cholangiopancreatography
- Registration Number
- CTRI/2015/06/005842
- Lead Sponsor
- Apollo Hospitals Bilaspur
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 93
Inclusion Criteria
ASA grade I and III
Exclusion Criteria
1.Patients with known sensitivity to study drugs
2.History of drug or alcohol abuse,
3.Morbid obesity (body mass index >40),
4.History of chronic pain or daily intake of analgesics
5.Oral anticoagulant use (warfarin)
6.Patients with bleeding diathesis
7.Impaired kidney or endocrinal functions
8.Pregnant patients and
9.Psychiatric patients
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Heart rate, systolic blood pressure, diastolic blood pressure, mean arterial pressure and oxygen saturation (SpO2)Timepoint: Basal, After study drug, After induction, at various time intervals during procedure, After procedure
- Secondary Outcome Measures
Name Time Method Total dose of propofol,Postoperative recovery in between two groups (modified Aldrete score) and any complication <br/ ><br>Timepoint: During and After procedure