Pre-eclampsia Clinical Trial
Official title:
A Randomised, Double-Blind, Placebo-Controlled, Flexible-Dose, Parallel-Group Study to Evaluate the Efficacy, Safety and Toleration of Oral Sildenafil Citrate Administered in the Dose Range of 20 - 80 Mg TID for the Treatment of Pre-Eclampsia. (PET)
To determine the efficacy and safety of sildenafil citrate in the treatment of established pre-eclampsia
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Status | Clinical Trial | Phase | |
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