study comparing between paracetamol and 6% hydroxy ethyl starch for decreasing pain induced by propofol injection during operatio
Not Applicable
- Conditions
- Health Condition 1: O- Medical and Surgical
- Registration Number
- CTRI/2023/05/052451
- Lead Sponsor
- DR KIRAN A V
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1.Aged between 18 to 60 years
2.ASA I and II category patients
3.Patients posted under general anaesthesia
4.Patients willing to give informed consent to participate in the study.
Exclusion Criteria
1.Anaphylaxis to the study drugs( 6% HES and paracetmol)
2.Chronic alcoholics and nicotine addiction
3.Patients with opioid drug intake for other comorbid conditions
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To compare the effectiveness of pretreatment with i.v. paracetamol with that of 6% hydroxy ethyl starch to reduce pain induced by propofol injection.Timepoint: 0 sec , 1 sec , 2 sec , 3 sec , 4 sec , 5 sec , 10 sec , 15 sec , 20 sec
- Secondary Outcome Measures
Name Time Method ILTimepoint: NI