Comparison of two doses of phenylephrine to prevent intra operative nausea and vomiting in pregnant patients posted for cesarean sectio

Not Applicable

Completed

• Conditions: Health Condition 1: O80- Encounter for full-term uncomplicated delivery

• Registration Number: CTRI/2021/08/035605
• Lead Sponsor: Departement of Anaesthesiology

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Completion: 2022-01-31
• Last Update Posted: 17 October 2022

Recruitment & Eligibility

• Status: Completed
• Sex: Not specified
• Target Recruitment: 195

Inclusion Criteria

Pregnant female patients with singleton pregnancy, taken up for Caesarean Section under spinal anaesthesia for various indications like previous Caesarean Section, breech presentation, cephalopelvic disproportion, pregnancy following infertility treatment, cord around neck, non progression of labour.

Exclusion Criteria

1. Patient refusal to participate in study

2. Emergency indication of Caesarean Section like antepartum haemorrhage, Placenta previa, abruptio placenta, fetal distress, obstructed labour, umbilical cord prolapse, preeclampsia, gestational diabetes, essential hypertension, more than two previous LSCS, history of PPH, multiple gestation.

3. Patients having contraindication for subarachnoid block.

4. Patient having associated systemic illness (hypo/hyperthyroidism, diabetic, neuromuscular disease ischaemic/ valvular/ congenital heart disease, psychiatric, hematological disorder, SLE).

5. History of seizures, coma, neurological signs or symptoms (Eclampsia)

6. Any allergy to local anaesthetic or any drug.

Study & Design

• Study Type: Interventional
• Study Design: Not specified