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Clotting ability of blood analysed by thromboelastography in healthy pregnant women undergoing Caesarean or vaginal delivery

A comparative study of thromboelastographic parameters in healthy pregnant women undergoing Caesarean or vaginal delivery

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2021/01/030570
Enrollment
140
Registered
2021-01-19
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: O00-O9A- Pregnancy, childbirth and the puerperium

Interventions

Control Intervention1: Thromboelastography and coagulation profile: Investigations in healthy pregnant women undergoing Caesarean or vaginal delivery

Sponsors

Lady Hardinge Medical College
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Healthy pregnant women >18 years posted for Caesarean delivery under spinal anaesthesia or vaginal delivery

Exclusion criteria

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

Design outcomes

Primary

MeasureTime frame
Proportion of healthy pregnant women having deranged thromboelastographic parameters 24 hours after Caesarean delivery and those after vaginal deliveryTimepoint: Predelivery, 24 hours after delivery and day of discharge—

Secondary

MeasureTime frame
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. 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—

Countries

India

Contacts

Public ContactDr Maitree Pandey

Department of Anaesthesiology Lady Hardinge Medical College

maitreepandey@gmail.com9810570515

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026