Clotting ability of blood analysed by thromboelastography in healthy pregnant women undergoing Caesarean or vaginal delivery
Not Applicable
- Conditions
- Health Condition 1: O00-O9A- Pregnancy, childbirth and the puerperium
- Registration Number
- CTRI/2021/01/030570
- Lead Sponsor
- ady Hardinge Medical College
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Healthy pregnant women >18 years posted for Caesarean delivery under spinal anaesthesia or vaginal delivery
Exclusion Criteria
1)Patients undergoing assisted vaginal delivery (use of forceps and vacuum)
2)Patients receiving preoperative unfractionated heparin, oral anticoagulants or magnesium sulphate
3)Patients with a history of deep vein thrombosis or more than two abortions
4)Patients with history of smoking
5)Patients with hereditary thrombophilia, anti-phospholipid syndrome
6)Patients with sepsis
7)Patients with platelet count < 1 lakh/ mm3
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Proportion of healthy pregnant women having deranged thromboelastographic parameters 24 <br/ ><br>hours after Caesarean delivery and those after vaginal deliveryTimepoint: Predelivery, 24 hours after delivery and day of discharge
- Secondary Outcome Measures
Name Time Method 1)Thromboelastographic parameters (Mean ± SD) pre-delivery, 24 hours post-delivery and on the day of discharge in healthy pregnant women after Caesarean or vaginal delivery. <br/ ><br>2)Correlation between platelet count, PT, INR, aPTT with MA, R and CI and D-dimer and BT with R, CI and TPI pre-delivery and 24 hr post-delivery in healthy pregnant women undergoing Caesarean delivery and vaginal delivery.Timepoint: Pre-delivery,24 hours post-delivery and on the day of discharge