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COMPARATIVE STUDY OF PREOPERATIVE USE OF ORAL ANALGESIC WITH AND WITHOUT INTRAVENOUS STEROID FOR POSTOPERATIVE PAIN, NAUSEA AND VOMITING IN PATIENTS OF CESAREAN SECTION UNDER SPINAL ANAESTHESIA.

Not Applicable
Completed
Conditions
Health Condition 1: O998- Other specified diseases and conditions complicating pregnancy, childbirth and the puerperium
Registration Number
CTRI/2019/04/018708
Lead Sponsor
Sachitha D
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Completed
Sex
Not specified
Target Recruitment
60
Inclusion Criteria

1) Women with singleton, uncomplicated pregnancy at term ( >37 completed weeks).

2) Women belonging to American society of anaesthesia category I-II and willing to give informed written consent.

3) Women scheduled to undergo elective cesarean delivery under spinal anesthesia

Exclusion Criteria

1) pregnancy with obstetric complications like hypertention, diabetes, oligohydramnios, polyhydramnios, antepartum haemorrhage, etc

Patients with contraindication to neuraxial anesthesia.

2) Patients known to be epileptics or on antiepileptic medications.

3) Patients with deranged renal function tests or liver function tests.

4) Patients with psychiatric disorder or unable to give consent.

5) Patients scheduled to undergo emergency cesarean delivery.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
1) Pain assessment using Numerical Rating Scale (NRS). <br/ ><br>2) PONV assessment using PONV Impact Scale Score. <br/ ><br>Timepoint: postoperative period <br/ ><br>
Secondary Outcome Measures
NameTimeMethod
1) Neonatal outcome using APGAR Score. <br/ ><br>2) Maternal Sedation using Ramsay Sedation Score. <br/ ><br>Timepoint: postoperative period
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