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OpenTrials
Completed

NCT Number: NCT07406776

Identification of Histories of Pregnancy Termination, Particularly Early Miscarriage, in General Medical Records

Early miscarriage (EM) is defined as the spontaneous expulsion of an intrauterine pregnancy of less than 14 weeks' duration. Early miscarriage is a very common complication, affecting more than 10% of pregnancies. Because of its frequency, EM is often considered a trivial event, particularly by healthcare professionals.

However, for the women who experience it, EM can be a traumatic event, difficult to discuss with their families, and a source of worries and questions for subsequent pregnancies. The international literature is consistent on the psychological morbidity associated with miscarriage: anxiety, depression and post-traumatic stress disorder have been studied in women following CPT. The identification of a history of EM by doctors is therefore important for the overall management of women's health.

The 2021 National Perinatal Survey showed that less than 5% of pregnant women in France had their first six months of pregnancy monitored by a general practitioner, a proportion that has been steadily declining in recent years. The majority of women are monitored by a gynecologist, or in 40% of cases by a midwife. These professionals therefore appear to be the preferred point of contact for women in the event of a miscarriage. In the absence of specific information, either from the woman herself or from the healthcare professional who treated her, the general practitioner-the attending physician may remain unaware of this event in their patient's life. Under these circumstances, identifying a history of EM in the general practitioner's medical records may not be sufficient.

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Key information

Age range

18 year–50 year

Sex eligibility

Female

Study type

Observational

Primary location

Gestonnairedu CURRS

Reims, Champagne-Ardenne, 51100, France

About this study

The primary objective is to describe the frequency of notification of a history of early miscarriage in the treating physician's medical record.

The secondary objectives are :

  • To describe how the treating physician is informed of the history of early miscarriage.
  • To investigate the factors associated with notification of a history of early miscarriage in the treating physician's medical record medical records.
  • Describe the frequency of notification of a history of termination of pregnancy other than early miscarriage (voluntary termination of pregnancy, foetal death in utero, medical termination of pregnancy) in the treating physician's medical record.
  • Describe the procedures for informing the attending doctor about the history of termination of pregnancy other than early miscarriage.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Female
  • Aged between 18 and 50
  • Whose GP has agreed to take part in the study
  • Agreeing to take part in the study.

Exclusion criteria

  • Minors
  • Over the age of 50
  • Protected by law (guardianship, curatorship, safeguard of justice)
  • Refusing to take part in the study.

Treatment and study plan

Primary outcomes

  1. notification of early miscarriage in the medical file of the woman who reported it.

    Time frame: Day 0

    the frequency of notification of a history of early miscarriage in the attending physician's medical records.

Sponsors and collaborators

Lead sponsor

Université de Reims Champagne-Ardenne

Other

Registry information

Important dates

Study start
2025
Primary completion
2025
Study completion
2026
First posted
Feb 12, 2026
Registry last updated
Feb 17, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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