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Comprehensive Assessment of Risks for Miscarriage.

Recruiting
Conditions
Spontaneous Abortion
Registration Number
NCT04456660
Lead Sponsor
Orthogyn Medical Center, Bulgaria
Brief Summary

This study aims to determine the role of serum biomarkers and placental bloodflow in the comprehensive evaluation of the risk for spontaneous abortion

Detailed Description

To study the added value (if any) of combining serum markers, immunologic factors, and ultrasound parameters in comprehensively evaluating the risk for spontaneous abortion.

Recruitment & Eligibility

Status
RECRUITING
Sex
Female
Target Recruitment
200
Inclusion Criteria
  • visualized fetal structures in utero & heart pulsations until 8th week of gestation
  • normal THS/T4 levels
  • no uterine malformations
  • BMI < 27
  • signed informed consent
Exclusion Criteria
  • fetal structures in utero & heart pulsations not visualized until the 8th week of gestation
  • elevated THS/T4 levels
  • uterine malformations
  • BMI > 27

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Occurence of a spontaneous abortionUp to 24 weeks of gestation

Absent heart rate pulsations on an ultrasound scan

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Orthogyn Medical and Dental Center

🇧🇬

Sofia, Bulgaria

Orthogyn Medical and Dental Center
🇧🇬Sofia, Bulgaria
Petar D Ignatov, PhD
Contact
00359888963189
ignatov@orthogyn.com

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