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Detecting bleeding problems in patients who develop very high BP during Pregnancy

Not Applicable
Conditions
Health Condition 1: O00-O9A- Pregnancy, childbirth and the puerperium
Registration Number
CTRI/2021/06/034324
Lead Sponsor
KMC Manipal
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot Yet Recruiting
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

For Cases - Singleton pregnancy with Severe Pre-eclampsia requiring immediate intervention

Controls - Singleton pregnancy with Pre-eclampsia that can undergo expectant

management

Exclusion Criteria

For Cases - Pre-eclampsia patients that can undergo expectant management, Multiple gestation, Any other causes of bleeding in pregnancy

For Controls - Multiple gestation, Any other causes of bleeding in pregnancy, Patients with severe pre eclampsia and eclampsia

Study & Design

Study Type
Observational
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Identification of type of coagulopathy based on scores of R value, K value, â??aâ?? angle, MA, CI, Ly30 <br/ ><br>â?¢ R value - Represents period of time of latency from start of test to initial fibrin formation <br/ ><br>â?¢ K time - Represents time taken to achieve a certain level of clot strength - equates to amplitude 20 mm <br/ ><br>â?¢ Alpha Angle Measures the rapidity of fibrin build-up and cross-linking (clot strengthening) <br/ ><br>â?¢ MA - represents the ultimate strength of the fibrin clot <br/ ><br>Timepoint: 4 months
Secondary Outcome Measures
NameTimeMethod
Providing Blood component as per result of TEG <br/ ><br>Further management as per protocol of hospital in high dependency unit.Timepoint: Outcome assessed every 8 weeks
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