Pyrimethamine, Sulfadiazine, and Leucovorin in Treating Patients With Congenital Toxoplasmosis

ConditionToxoplasmosis
Trial statusRecruiting
Trial phasePhase 4
Trial typeInterventional
Biological sexAll
AgeNot listed
SponsorNational Institute of Allergy and Infectious Diseases (NIAID)

About this trial

RATIONALE: Congenital toxoplasmosis is an infection caused by the parasitic organism Toxoplasma gondii, and it may be passed from an infected mother to her unborn child. The mother may have mild symptoms or no symptoms; the fetus, however, may experience damage to the eyes, nervous system, skin, and ears. The newborn may have a low birth weight, enlarged liver and spleen, jaundice, anemia, petechiae, and eye damage. Giving the antiparasitic drugs pyrimethamine and sulfadiazine is standard treatment for congenital toxoplasmosis, but it is not yet known which regimen of pyrimethamine is most effective for the disease.

PURPOSE: Randomized phase IV trial to determine which regimen of pyrimethamine is most effective when combined with sulfadiazine and leucovorin in treating patients who have congenital toxoplasmosis.

Eligibility criteria

Qualifiers

Infants with congenital toxoplasmosis Toxoplasma gondii confirmed prior to age 2.5 months

Pregnant women with evidence of toxoplasma infection by clinical observation and amniotic fluid sampling

Acute infection acquired during gestation with evidence of fetal infection

Untreated older children entered as controls

Disqualifiers

None

Trial design

Treatments tested in this trial

  • Leucovorin calcium
  • Pyrimethamine
  • Spiramycin
  • Sulfadiazine

Treatment groups

600 Participants
are divided into 2 treatment groups

Sponsors and collaborators