TO SEE THE EFFECT OF LOW DOSE INTRAVENOUS KETAMINE ON PAIN FOLLOWING CAESEREAN SECTION UNDER SPINAL ANAESTHESIA.

Phase 2

• Conditions: Health Condition 1: O82- Encounter for cesarean delivery without indication

• Registration Number: CTRI/2020/02/023498
• Lead Sponsor: Bangalore medical college and research institute

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 24 November 2021

Recruitment & Eligibility

• Status: ot Yet Recruiting
• Sex: Not specified
• Target Recruitment: 0

Inclusion Criteria

1.Parturients who give written informed consent.

2.ASA physical status classes I and II)

3.Age between 19- 35 years

4.Primigravida or multigravida undergoing lower segment caesarean section for the first time.

5.Parturients with uncomplicated full term singleton pregnancy

Exclusion Criteria

1.Parturients refusing to participate in the study .

2.ASA physical class >II

3.Parturients with height <150 cms

4.Parturients with (1) Hypertensive disorders of pregnancy , essential hypertension (2) Anaemia, (3) previous abdominal surgeries, (4) diabetes mellitus, (5) Cardiac disease (8) Abruptio placenta, placenta previa (9) features of increased intracranial pressure

5.Any contraindication to spinal anaesthesia,

6.Known allergy to ketamine or local anaesthetics .

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
to assess the effect of single low dose of ketamine intravenously in cesarean section under spinal anaesthesia after delivery of the baby in reducing the incidence of breakthrough pain postoperativelyTimepoint: Pain assessed every 30 min for 6 hrs post caeserean section.

Secondary Outcome Measures

Name	Time	Method
the possibility of prolongation of duration of spinal anaesthesia .Timepoint: Duration of sensory and motor blockade assessed every 30 min post operatively till 6hrs post caeserean section.