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Clinical Trials/CTRI/2018/10/016128
CTRI/2018/10/016128
Recruiting
未知

To investigate correlation between raised serum bile acid levels in pregnancies affected with Intrahepatic Cholestasis of Pregnancy and adverse perinatal outcome. - IHCP40

Max Smart Super Speciality Hospital0 sites0 target enrollmentTBD

Overview

Phase
未知
Intervention
Not specified
Conditions
Health Condition 1: O266- Liver and biliary tract disordersin pregnancy, childbirth and the puerperium
Sponsor
Max Smart Super Speciality Hospital
Status
Recruiting
Last Updated
4 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
4 years ago
Study Type
Observational

Investigators

Eligibility Criteria

Inclusion Criteria

  • Pregnant women presenting with pruritis with elevated liver enzymes
  • Primigravida or Multigravida
  • Spontaneous or IVF conception
  • Singleton or Twins

Exclusion Criteria

  • History of cholelithiasis
  • Chronic liver disease
  • Hepatitis A,B,C,E
  • Any other cause of raised liver function tests
  • Dermatological cause of pruritis
  • Allergic disorder
  • Pre eclampsia and HELLP
  • Patient refusal
  • Patient with pruritis but no elevation of liver enzymes
  • Pregnancy ending before 24 weeks gestation

Outcomes

Primary Outcomes

Not specified

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