CTRI/2021/11/037798
Completed
未知
To compare the efficacy of two different doses of IV dexmedetomidine for controlling post-operative shivering in women undergoing caesarean delivery under spinal anaesthesia: a prospective, randomized, double blind, parallel group, controlled clinical trial
Koldinne Jagadeeswara Reddy0 sites80 target enrollmentTBD
Overview
- Phase
- 未知
- Intervention
- Not specified
- Conditions
- Health Condition 1: O00-O9A- Pregnancy, childbirth and the puerperium
- Sponsor
- Koldinne Jagadeeswara Reddy
- Enrollment
- 80
- Status
- Completed
- Last Updated
- 3 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •Parturients with BMI 18\-35kg/m2 undergoing
- •caesarean delivery under spinal anaesthesia
Exclusion Criteria
- •Patients refusal
- •Allergy and contraindication to the study drug
- •(Dexmedetomidine)
- •Patients belonging to ASA grade III and above.
- •BMI \<18 to \> 35kg/m2
- •Twin / multiple pregnancy
- •History of chronic nausea or itching /pruritis
- •during pregnancy
- •Psychiatric and mentally retarded patients
Outcomes
Primary Outcomes
Not specified
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