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This trial is complete. It is no longer accepting participants.

NCT00004399

NCT00004399
Completed Not Applicable

Who may be able to join

Who might be able to join this trial:

  • You have been diagnosed with severe preeclampsia (a serious pregnancy complication) and are at risk of seizures
  • Your blood pressure is higher than 160/110 mmHg, or your average arterial blood pressure reading is 126 mmHg or above
  • Your urine tests show a large amount of protein (more than 5 grams over 24 hours)
  • You have pain in your upper abdomen or upper right side, or your liver enzyme levels are significantly elevated (confirm with trial site)
  • You have severe headaches and/or visual disturbances such as blind spots
  • Your blood platelet count is very low (below 100,000), or you have signs of abnormal blood clotting or red blood cell damage
  • Your urine output is very low (less than 400 mL per day or 30 mL per hour)
  • You have fluid buildup in your lungs (pulmonary edema)

Who may not be able to join:

  • You have previously used or are currently using magnesium sulfate or a type of blood pressure medication called dihydropyridines
  • You are currently taking any other anti-seizure medications
  • You have severe kidney failure
  • You have a history of chest pain (angina) or a heart attack
  • You have any heart problems or abnormal heart rhythms, particularly a heart rate below 60 beats per minute
  • You have a history or signs of heart failure
  • You have a serious mental or physical condition that could affect your treatment
  • You are allergic to drugs with a similar chemical structure to nimodipine or magnesium sulfate
  • There are signs of distress or abnormalities detected in your unborn baby

Important: Always verify eligibility with the trial site directly before applying.

Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.

Trial details

Status
Completed
Phase
Not Applicable
Sponsor
FDA Office of Orphan Products Development
Registry
clinicaltrials_gov
Start date
1 September 1995

Can't join this trial?

Expanded access pathways

If this trial is not available to you, other access pathways may exist. In Australia, the TGA Special Access Scheme allows access to unapproved therapeutic goods for individual patients.

TGA Special Access Scheme information

Find other recruiting trials on ClinicalTrials.gov

Data last synced from ClinicalTrials.gov: 30 June 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.

View original record on ClinicalTrials.gov