Viewing Study NCT00329693



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Last Modification Date: 2024-10-26 @ 9:25 AM
Study NCT ID: NCT00329693
Status: COMPLETED
Last Update Posted: 2011-05-19
First Post: 2006-05-23

Brief Title: Study Assessing the Effect of 3-week Treatment With One of Three Oral Doses of Quinagolide
Sponsor: Ferring Pharmaceuticals
Organization: Ferring Pharmaceuticals

Study Overview

Official Title: A Randomised Double-blind Parallel Groups Dose-finding Placebo-controlled Multi-centre Proof of Concept Study Assessing the Effect of 3-wk Treatment With 1 of 3 Oral Doses of Quinagolide Placebo in Preventing Ovarian Hyperstimulation Syndrome in Women Undergoing Controlled Ovarian Hyperstimulation
Status: COMPLETED
Status Verified Date: 2011-05
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: Women included in this study are undergoing controlled ovarian hyperstimulation for assisted reproductive technologies ART and present with signs of moderate risk of developing OHSS
Detailed Description: No data to be entered

Study Oversight

Has Oversight DMC: None
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?: None