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Comparison on the effect of intravenous Tramadol and low-dose Ketamine in controlling post -spinal anaesthesia shivering following caeserean sectio

Phase 3
Conditions
Health Condition 1: O748- Other complications of anesthesiaduring labor and delivery
Registration Number
CTRI/2023/08/056964
Lead Sponsor
Merlin Marita Loving
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot Yet Recruiting
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

1.Pregnant women of age group 18-45 years

 2.Patients of ASA I or II

Exclusion Criteria

1. Patients with history of allergy to the study drugs (tramadol, ketamine)

2. Patients with history of diabetes, hypertension, cardiovascular, respiratory, renal or neurological disease      

3.  Patients with spinal deformity

4.  Patients with local site infection

5. Patients with bleeding disorder- platelet count <50,000/microlitre, prothrombin time >14 sec, International normalized ratio (INR) > 1.5

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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