A clinical trial to study the incidence and intensity of injection pain of two different formulations of drug propofol in patients requirin general anaesthesia
Not Applicable
Completed
- Conditions
- Health Condition 1: null- ASA 1 and ASA 2
- Registration Number
- CTRI/2018/04/013125
- Lead Sponsor
- SDM College of Medical Sciences and Hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 200
Inclusion Criteria
1.The subjects who are aged between 18 to 60 years belonging to ASA Physical status 1 and 2.
2. Those willing to participate.
Exclusion Criteria
1.Patients with ischaemic heart diseases, neurological or psychiatric problems, renal or hepatic insufficiency, suspected or known airway difficulty.
2. Pregnant or lactating women.
3. Those who were taking any analgesics before surgery.
4. Those with known hypersensitivity to propofol or to any of the constituents of emulsion.
5. Those who refuse to give consent.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method