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Sildenafil Citrate and Intrapartum Fetal Distress

Fetal Distress Clinical Trial

Official title:
Efficacy of Sildenafil Citrate to Reduce the Rate of Cesarean Section for Intrapartum Fetal Distress During Induction of Labor

Clinical Trial Summary

Induction of labour (IOL) is done for 20% of pregnancies for various maternal and fetal indications and nearly 20% of labour inductions end up in caesarean section. The most common causes are failed induction and intrapartum fetal distress. In spite of significant advances in methods of IOL and intrapartum fetal monitoring, no interventions are proven to reduce the development of intrapartum fetal distress

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT04325243
Study type Interventional
Source Assiut University
Contact
Status Completed
Phase Phase 4
Start date September 1, 2020
Completion date July 31, 2022
View Details
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