CTRI/2021/10/037589Completed未知
Phenylepherine, ondensetron or a combination of both for prevention of intraoperative nausea and vomiting in patients undergoing lower segment caesarean section :a prospective ,double blind randomized control trial
Trial Snapshot
- Phase
- 未知
- Status
- Completed
- Sponsor
- DEPARTMENT OF ANESTHESIA
- Enrollment
- 195
Study Overview
Brief Summary
No summary available.
Study Design
- Study Type
- Interventional
Eligibility Criteria
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.
Investigators
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