Status:
WITHDRAWN
Comparison of Different Doses of Clonidine to Fentanyl as an Adjuvant to Bupivacaine 0.5% for Spinal Anesthesia
Lead Sponsor:
Pravara Institute of Medical Sciences University
Conditions:
Full Term Pregnant Patients
Undergoing Lower Segment Caesarian Section
Eligibility:
FEMALE
20-35 years
Phase:
NA
Brief Summary
The purpose of this study is to evaluate the safety, quality and duration of block with the addition of Clonidine in different doses to 0.5% heavy bupivacaine, and to compare it with addition of Fenta...
Detailed Description
All the patients selected for study will have a detailed general examination including airway assessment, spine, and systemic examination .Patient will be kept nil-by-mouth for 6 to 8 hours. Sedatives...
Eligibility Criteria
Inclusion
- Undergoing Lower Segment Caesarian Section
- ASA grade I or II
- Not having any complicated pregnancy
- Not having any systemic disorders.
- Age group 20 - 35 years
Exclusion
- Not willing for spinal anaesthesia
- Unwilling to get enrolled in this study.
- Complicated pregnancy like pregnancy induced hypertension, placenta previa, abruptio placenta.
- Systemic disorders like diabetes, heart disease, chronic hypertension, pulmonary disease
- With acute fetal distress.
- With bleeding or coagulation disorders.
- Maternal haemorrhage leading to hypovolemia.
- Height less than 145 cms
Key Trial Info
Start Date :
August 1 2010
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
November 1 2011
Estimated Enrollment :
Patients enrolled
Trial Details
Trial ID
NCT01205204
Start Date
August 1 2010
End Date
November 1 2011
Last Update
September 21 2017
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