A clinical study to find the effect of ketamine to reduce labour pai
Not Applicable
- Conditions
- Health Condition 1: O80- Encounter for full-term uncomplicated delivery
- Registration Number
- CTRI/2022/05/042788
- Lead Sponsor
- SRM Medical college hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Open to Recruitment
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
All consenting primigravidae having normal vaginal delivery, assessed under ASA 1 and 2, weight between 50 to 100kgs, height more than 150cm and less than 180cm, singleton pregnancy with cephalic presentation with 3cm cervical dilatation after obstetricians approval.
Exclusion Criteria
patients who refuse to participate in the study, patients with epilepsy,hyperthyroidism,liver, cardiac,renal disease, coagulation abnormalities and contraindications to epidural anaesthesia.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To study the VAS score during second stage of labourTimepoint: Pain will be assessed by visual analogue scale every 30 minutes during labour and continued for 1 hour after baby delivery
- Secondary Outcome Measures
Name Time Method 1. changes in haemodynamic parameters <br/ ><br>2. APGAR score <br/ ><br>3. Frequency of adverse effectsTimepoint: 1. The heart rate, mean arterial pressure and oxygen saturation will be monitored continuously and recorded every 30 min during the second stage of labour. <br/ ><br>2. The APGAR score at 1 minute and 5 minutes will be recorded. <br/ ><br>3.Adverse effects will be noted and graded according to severity.