Viewing Study NCT02782559


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Study NCT ID: NCT02782559
Status: WITHDRAWN
Last Update Posted: 2018-03-27
First Post: 2016-02-11
Is Gene Therapy: True
Has Adverse Events: False

Brief Title: Efficacy of Sildenafil in Preterm Preeclampsia
Sponsor: The University of Texas Health Science Center, Houston
Organization:

Study Overview

Official Title: Randomized Double-Blind, Placebo Controlled Evaluation of the Efficacy of Sildenafil Versus Placebo in Preterm Preeclampsia
Status: WITHDRAWN
Status Verified Date: 2018-03
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: difficulties acquiring the drug and funding for the drug
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: SIL
Brief Summary: Randomized controlled trial to assess efficacy of Sildenafil in addition to expectant management for the treatment of preterm preeclampsia
Detailed Description: Preeclampsia is a major cause of maternal mortality. When preeclampsia presents prior to thirty-four weeks of gestation, expectant management is the standard practice in stable patients with the goal of extending pregnancy and therefore decreasing the risk of adverse outcomes in the premature neonate. Our aim was to assess the efficacy of Sildenafil, a phosphodiesterase inhibitor, versus placebo, in addition to expectant management, for the treatment of preterm preeclampsia to prolong pregnancy.

Study Oversight

Has Oversight DMC: True
Is a FDA Regulated Drug?: None
Is a FDA Regulated Device?: None
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: