Status:

COMPLETED

Evaluation of Serum Levels of C Reactive Protein (CRP) and Its Correlation With Fetal Ultrasound Parameters in the Prediction of Threatened Miscarriage in the First Trimester

Lead Sponsor:

Al-Azhar University

Conditions:

Threatened Miscarriage

Eligibility:

FEMALE

20-35 years

Brief Summary

The goal of this observational study is to evaluate and compare in pregnant women with threatened miscarriage in the first trimester. The main questions it aims to answer are: What is the correlation...

Detailed Description

This observational study will enroll 100 pregnant women, with 50 in the threatened miscarriage group and 50 healthy controls, to compare serum C reactive protein (CRP) levels and fetal ultrasound find...

Eligibility Criteria

Inclusion

  • All pregnant women in the age group (20-35) between 7 and 13 weeks gestation in which a singleton embryo with evident cardiac activity with sure last menstrual period (LMP) constant with 1st trimester documented ultrasound
  • The included subjects will be divided into two groups:-
  • Group 1 (control) will consist of 50 pregnant women with uneventful pregnancies without any problem.
  • Group 2 (patients) will consist of 50 pregnant women with threatened miscarriage, of them.

Exclusion

  • Multiple pregnancies.
  • Women having received hormonal treatment or progesterone supplements.
  • Pregnancies with a difference of more than 7 days between last menstrual period (LMP) and crown- rump length.
  • History of general medical disease e.g. diabetes, thyroid disease or antiphospholipid syndrome, Presence of local (gynecological) disease e.g. fibroid or adnexal masses verified by normal appearance of the uterus and ovaries by ultrasound.
  • Presence of uterine malformations e.g. hypoplastic uterus or septate uterus diagnosed by history of recurrent miscarriage, hysterosalpingography or 3D ultrasound, Intake of natural or synthetic progesterone.
  • Obesity.
  • Ectopic pregnancy
  • Vesicular mole
  • Fetal demise by Ultrasound

Key Trial Info

Start Date :

July 1 2022

Trial Type :

OBSERVATIONAL

Allocation :

ACTUAL

End Date :

October 1 2023

Estimated Enrollment :

100 Patients enrolled

Trial Details

Trial ID

NCT06011057

Start Date

July 1 2022

End Date

October 1 2023

Last Update

December 12 2023

Active Locations (1)

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Page 1 of 1 (1 locations)

1

Al-Hussein University Hospital

Cairo, Egypt, 11633