A clinical trial to study the effect of spinal morphine in reducing the requirement of locally anesthetizing drugs in labour analgesia
Not Applicable
- Registration Number
- CTRI/2020/03/024119
- Lead Sponsor
- AIIMS New Delhi
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Open to Recruitment
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1.ASA I and II
2.Primi gravida/ Mutigravida, para 0
3.Uncomplicated singleton pregnancy
4.Vertex presentation
5.Active labour
6.Requesting for labour analgesia
Exclusion Criteria
- Local or systemic infection
- Patient not willing to participate
- Known allergy to study drugs
- Bleeding disorders
- Decreased platelet counts
- Usage of opioids/other analgesics in last 4hours
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Effect of intrathecal morphine on Local anaesthetic requirement epidurally during labourTimepoint: Every 30 minutes till delivery, then every 6 hours postnatal till 24 hours.
- Secondary Outcome Measures
Name Time Method Effect of intrathecal morphine on <br/ ><br>1. Pain scores by VAS in I, II and III stages of labour <br/ ><br>2.Incidence of maternal nausea and vomiting , urinary retention and pruritus <br/ ><br>3.Rate of instrumental delivery <br/ ><br>4.APGAR scores at 1 , 2 and 5 minutes <br/ ><br>5. Maternal satisfaction (assessed by a subjective scale) <br/ ><br>Timepoint: Every 30 minutes till delivery and then postnatal every 6 hours for 24 hours.