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Clinical Trials/NL-OMON51730
NL-OMON51730RecruitingNot Applicable

Assessment of cervical SofTening and the Prediction of Preterm birth - STIPP study

Academisch Medisch Centrum0 sites390 target enrollmentStarted: TBDLast updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Recruiting
Enrollment
390

Study Overview

Brief Summary

No summary available.

Study Design

Study Type
Observational

Eligibility Criteria

Inclusion Criteria

  • - Age 18 years or above.
  • - Ability to understand Dutch or English (both spoken and written).
  • - Ultrasound-based gestational age determined by measurement of crown rump
  • length (CRL) determined between 9 and 11 weeks of gestation.
  • - Singleton and twin pregnancies.
  • - Medical history of spontaneous PTB before 34 weeks of gestation OR
  • Threatened PTB between 24 and 34 weeks of gestation.

Exclusion Criteria

  • - Under 18 years of age.
  • - Signs of intrauterine infection.
  • - Obstetric indication for immediate delivery (advanced labor, cord prolapse,
  • abruption, signs of fetal distress).
  • - Confirmed fetal abnormality.
  • - Confirmed preterm rupture of membranes.
  • - Confirmed vasa / placenta praevia.
  • - Severe vaginal bleeding and light bleeding that cannot be stopped.
  • - Signs of imminent labor such as blood loss, regular contractions.

Investigators

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