Comparision between effects of 6% hydroxyethyl starch and dexmedetomidine pre-administration in reducing pain on propofol injection : A randomized controlled double blinded clinical trial
Not Applicable
- Conditions
- Health Condition 1: O- Medical and SurgicalHealth Condition 2: O- Medical and Surgical
- Registration Number
- CTRI/2023/06/054175
- Lead Sponsor
- Dr Arun Kumar
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1.Patients of ASA status 1 and 2.
2.Patients between 18 to 60 years of age.
3.Either sex.
4.Patients will come for elective surgery under
general anaesthesia.
Exclusion Criteria
1.Patients of ASA status more or equal to 3.
2.Patients with difficulty in communication.
3.Patients allergic to propofol or 6% hydroxyethyl
starch or dexmedetomidine.
4.Patients in whom hand or forearm veins will be
not accessible and 18 G IV cannula can not be
inserted.
5.Emergency surgeries.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To compare the effects of preadministration of 6 percent hydroxyethyl starch & dexmedetomidine in reducing pain on propofol injectionTimepoint: 90 seconds
- Secondary Outcome Measures
Name Time Method To look for any side effects of the 6 percent hydroxyethyl starch & dexmedetomidineTimepoint: 90 seconds