se of two drug single or combination for prevention of nausea vomiting in caesarea

Not Applicable

Completed

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

• Registration Number: CTRI/2021/10/037589
• Lead Sponsor: DEPARTMENT OF ANESTHESIA

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Completion: 2022-02-14
• Last Update Posted: 6 February 2023

Recruitment & Eligibility

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

Inclusion Criteria

This study will be carried out in term pregnant female patients with singleton pregnancy, taken up for elective 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 subarchnoid block.

4.Patient having associated systemic illness (hypo/hyperthyroidism, diabetic, neuromuscular disease ischemic/ 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.

H/o PONV

Study & Design

• Study Type: Interventional
• Study Design: Not specified