PTSD after a first-trimester miscarriage

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This prospective, questionnaire-based study enrolls women with spontaneous miscarriage up to 14 weeks gestation and combines medical record review with self-administered instruments. Participants complete validated questionnaires (IES-R, PCL-S, and TRM) during hospitalization to capture symptoms over the past week and month. Questionnaire scores will be used to estimate the prevalence and severity of PTSD-related symptoms in the cohort. The goal is to identify women who could benefit from early psychological support and to inform clinical care after early pregnancy loss.

Why it matters

Who can join: the full rules

Inclusion Criteria:

* spontaneous abortion
* gestational age up to 14 weeks.

Exclusion Criteria:

* none

Where it's running

• Jagiellonian University Medical College, Department of Gynecology and Obstetrics
  Krakow, Malopolska, Poland Recruiting

Study contacts

• Study coordinator: Iwona Gawron, PhD, MD
• Email: iwona.gawron@uj.edu.pl
• Phone: +48 12424870

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How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.