A clinical trial to study the effects of estradiol as compared to EMLA cream on pain due to puncturing the vein and easiness during inserting cannula in obese female patients.
Not Applicable
- Conditions
- Health Condition 1: null- Pts of ASA I& II,Female pts undergoing any elective surgery,Age between 25 -65 years,Body Mass Index 30kg/mt2,Hemodynamically stable.
- Registration Number
- CTRI/2014/11/005162
- Lead Sponsor
- A
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Open to Recruitment
- Sex
- Not specified
- Target Recruitment
- 132
Inclusion Criteria
Pts of ASA I& II,
Female pts undergoing any elective surgery,
Age between 25 -65 years,
Body Mass Index > 30kg/mt2,
Hemodynamically stable,
Exclusion Criteria
Pts with a h/o HTN, DM, Liver disease, Renal Failure, peripheral neuropathy, psychiatric disorders.
Pts on sedatives, hypnotics, antidepressants, estradiol, analgesic & drugs with effects on the nervous system.
Pts allergic to estradiol.
Patientâ??s refusal.
Abnormal skin condition (broken skin, infection, scar psoriasis, eczema) at the site of VP.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Incidence & severity of Venous cannulation pain and number of first attempt failure.Timepoint: immediatly after venous cannulation.
- Secondary Outcome Measures
Name Time Method incidence of side effects.Timepoint: for 24 hrs