Comparison of Intravenous Phenylephrine and Noradrenaline in management of Spinal Anaesthesia Induced Hypotension in Elective Cesarean Sectio
- Conditions
- Health Condition 1: 1- Obstetrics
- Registration Number
- CTRI/2022/08/044815
- Lead Sponsor
- RGKar Medical College and Hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
1. ASAI II
2. Patients aged 18 and above .
3. Patients undergoing elective and emergency caesarean section under spinal anaesthesia
4. Patients showing hypotension after spinal anaesthesia
1. ASA III, IV
2. Any spine abnormalities
3. Patient refusal
4. Patient with bleeding disorder
5. Patient in active labour
6. GDM,PIH
7. Height < 140cm and >180cm
8. Allergy in drug use in thesis.
9. Eclampsia and severely preeclampsia
10. Uncontrolled diabetes
11. Patients with coagulopathy secondary to antiblastic cancer therapy
12. Cardiac or neurological diseases
13. Known allergy to the anaesthetic drugs used
14. Bowl obstruction
15. Systemic sepsis
16. Failed/patchy block will be converted into General Anaesthesia and will not be included in the study
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To compare the effectiveness between Phenylephrine and Noradrenaline via intravenous route in preventing spinal anaesthesia induced hypotension in elective LUCSTimepoint: 6 month after approval of ethical committee
- Secondary Outcome Measures
Name Time Method To observe any side effectof the drug eg.- bradycardia, tachycardiaTimepoint: 6 month after approval of ethics committee