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Pregnancy and Congenital Toxoplasmosis (GRETA)

Civil Hospices of Lyon logo

Civil Hospices of Lyon

Status

Completed

Conditions

Retinochoroiditis
Congenital Toxoplasmosis

Treatments

Other: Estimation of the occurrence of retinochoroiditis in women with congenital toxoplasmosis and previous retinochoroiditis lesions (recurrence) during pregnancy and postpartum.

Study type

Observational

Funder types

Other

Identifiers

NCT05774496
2022-A02496-37 (Other Identifier)
69HCL22_1041

Details and patient eligibility

About

The Toxoplasma gondii parasite causes toxoplasmosis. It is characterized by persistent cysts mostly localised in the brain and ocular areas. In the case of immunodeficiency, those cysts are likely to reactivate. During pregnancy, an infection exposes the foetus to a variety of consequences, from severe neurologic lesions to subclinical forms at birth. However, those forms are likely to complicate at any age to toxoplasmic retinochoroiditis, that can unpredictably recur with severe functional consequences. Pregnancy may stimulate lesions or their recurrences, putting the foetus at risk of contamination because of the release of tachyzoites in the bloodstream. The occurrence of these complications is poorly known, especially with congenital toxoplasmosis. Nevertheless, this information is essential to take care of patients, particularly women with congenital toxoplasmosis, usually worried about the consequences of a pregnancy.

As a precaution, women with congenital toxoplasmosis follow a specific ophthalmologic, and trimonthly monitoring, composed of fundus examinations during pregnancy and in postpartum. To eliminate the contamination risk, serological examinations at birth and one year later are done on their kids.

The aim of this study is to estimate the risk of toxoplasmic retinochoroiditis during pregnancy and the impact on their children. Retrospective and prospective data from the Lyon Cohort of Maternal and Congenital Toxoplasma Infections will be used.

As a result of to this study, the investigators expect to provide better information to women suffering from congenital toxoplasmosis about their own ocular safety during pregnancy, and the safety of their child(ren). The investigators seek to provide new national and international recommendations about these patients and their children's care.

Enrollment

76 patients

Sex

Female

Ages

21 to 50 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Being a woman
  • Born before March 2022
  • Suffering from congenital toxoplamosis

Exclusion criteria

  • Refusal to give informed consent
  • Any condition that would limit the ability of the patient to give consent
  • Psychiatric cares
  • To be deprived of liberty
  • To be under administrative supervision

Trial design

76 participants in 1 patient group

Congenital toxoplasmosis women
Description:
Women older than 21 suffering from congenital toxoplasmosis, with or without children.
Treatment:
Other: Estimation of the occurrence of retinochoroiditis in women with congenital toxoplasmosis and previous retinochoroiditis lesions (recurrence) during pregnancy and postpartum.

Trial contacts and locations

1

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Central trial contact

Martine Wallon, MD,PhD,PUPH; Justine Sales, MSc Student

Data sourced from clinicaltrials.gov

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