A clinical study to see the impact of phenylephrine drug infusion on body temperature during spinal anesthesia in parturients undergoing caesarean sectio
Not Applicable
- Conditions
- Health Condition 1: O- Medical and Surgical
- Registration Number
- CTRI/2024/02/062506
- Lead Sponsor
- All India Institute of Medical Sciences Patna
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Pregnant women 18-45 years of age planned for cesarean section under spinal anesthesia will be included in the study.
1.Age between 18 and 65 years
2.ASA-PS Grade 2
Exclusion Criteria
Patient refusal to participate in the study
Hypertensive disorders of pregnancy
Cardiac diseases
Antepartum haemorrhage
Known allergy to drugs
Thyroid disease
Raynaud’s Disease
Fever
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To evaluate the change in core temperature with and without phenylephrine infusion using an infrared tympanometer in patients undergoing cesarean section under spinal anesthesiaTimepoint: Just before induction till end of surgery.
- Secondary Outcome Measures
Name Time Method To evaluate the differences in surface temperature with and without phenylephrine <br/ ><br>To compare the incidence and severity of shivering <br/ ><br>To evaluate the incidence and frequency of bradycardia and hypotension <br/ ><br>To determine APGAR scores at one and five minutesTimepoint: Just before induction till end of surgery