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UnknownNCT03177824

Sildenafil Citrate for Treatment of Growth-restricted Fetuses

Status
Unknown
Phase
Phase 3
Study type
Interventional
Enrollment
60 (estimated)
Sponsor
Ain Shams University · Academic / Other
Sex
Female
Age
20 Years – 40 Years
Healthy volunteers
Not accepted

Summary

The aim of this study is to assess the effect of Sildenafil citrate therapy on neonatal outcomes in women with fetal growth restriction.

Conditions

Interventions

TypeNameDescription
DRUGSildenafil Citrate 25Mg TabGroup 1, consists of 30 patients who will receive Sildenafil citrate (25mg) tab (Silden, Epico, Egypt) 3times daily till the time of delivery, followed by repeating the Doppler US scan serially to detect changes in the measured indices and then assess the neonatal outcome after delivery as regard birth weight and APGAR score.
DRUGPlacebo Oral TabletGroup 2, consists of 30 patients receiving placebo Oral Tablet 3times daily , followed by repeating the Doppler US scan serially to detect changes in the measured indices and then assess the neonatal outcome after delivery as regard birth weight and APGAR score

Timeline

Start date
2017-03-30
Primary completion
2017-09-30
Completion
2017-10-01
First posted
2017-06-06
Last updated
2017-06-09

Locations

1 site across 1 country: Egypt

Source: ClinicalTrials.gov record NCT03177824. Inclusion in this directory is not an endorsement.

Sildenafil Citrate for Treatment of Growth-restricted Fetuses (NCT03177824) · Clinical Trials Directory