se of multiple drugs to reduce pain of propofol injectio
Phase 4
- Conditions
- Health Condition 1: O- Medical and Surgical
- Registration Number
- CTRI/2022/11/047602
- Lead Sponsor
- Mysore Medical college and Research Institute
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1.Patients undergoing elective surgeries under general anaesthesia.
2.Belonging to American Society of Anaesthesiologists (ASA) Physical status
I or II.
3.Patients who are willing to sign written informed consent form.
Exclusion Criteria
1.Patients belonging to ASA III and IV physical status.
2.Patients with known cardiac disorders, other systemic disorders of lung and liver.
3.Pregnant patients
4.Patients for emergency procedures.
5.Those allergic to Propofol and study drugs
6.Those with history of motion sickness
7.History of post- operative nausea and vomiting
8.Patients in nasogastric tube and patients with difficult airway.
9.Patient refusal
10.History of taking any analgesic before surgery
11.Neurological deficit
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Attenuation of propofol induced pain during induction of anaesthesia.Timepoint: Pain is assessed at baseline, 5 seconds 10 seconds, 15 seconds, 20 seconds, 25 seconds and 30 seconds during induction of anaesthesia using propofol injection
- Secondary Outcome Measures
Name Time Method nilTimepoint: nil