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NCT01417195 · ClinicalTrials.gov registry record · Phase 4

Menopur Mixed Protocol

A Phase 4 study of Infertility, sponsored by Ferring Pharmaceuticals.

Completed
Registry status
Phase 4
Development phase
122
Enrollment target
10
Study locations

NCT01417195 is a Phase 4 study of Infertility that has completed, run by Ferring Pharmaceuticals. The registered enrollment target is 122 participants, below the 7,588-participant average among 74 other Infertility trials with a reported enrollment target (98% lower). The trial reports 10 study locations across 7 states.

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The verdict

NCT01417195, a Phase 4 study of Infertility, has completed, sponsored by Ferring Pharmaceuticals.

COMPLETED
Registry status
Phase 4
Development phase
122 participants
Enrollment target
10
Study locations

Study Summary

The objective of this study was to compare the fertilization rate between the combination of Menopur and Bravelle mixed in the same syringe and Menopur alone, both administered subcutaneously (SC), in subjects undergoing Assisted Reproductive Technology (ART). Additionally the study assessed subjects' ability to mix and store the combination of Menopur and Bravelle and to assess safety of the Menopur and Bravelle combination.

Conditions Studied

Interventions

  • DRUG Bravelle
  • DRUG Menopur

Study Locations (10)

Texas

  • The Center for Assisted Reproduction - Bedford
  • Houston Fertility Institute - Houston
  • Center of Reproductive Medicine - Webster

Illinois

  • Fertility Center of Illinois - Chicago
  • The Advanced IVF Institute - Naperville

Colorado

  • Colorado Center for Reproductive Medicine - Lone Tree

Florida

  • Women's Medical Research Group - Clearwater

Georgia

  • Reproductive Biology Associates - Atlanta

Maryland

  • Shady Grove Fertility - Rockville

Washington

  • Seattle Reproductive Medicine - Seattle

Trial Details

FieldValue
Enrollment Target 122 participants
Start Date 2011-07
Est. Completion 2012-01
Phase Phase 4

Sponsor

Ferring Pharmaceuticals

83 total trials

What the Registry Record Tells You About NCT01417195

The ClinicalTrials.gov registry entry for NCT01417195 describes a study currently listed as completed, categorized as Phase 4. The registered enrollment target is 122 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 7,588-participant average among 74 other Infertility trials with a reported enrollment target (98% lower). The listed sponsor is Ferring Pharmaceuticals, which has 83 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Infertility appearing as the primary indexed condition, and to 2 interventions - of which Bravelle is the first listed.

NCT01417195 reports 10 study locations spanning 7 distinct geographic areas - top geographies include Texas, Illinois, Colorado.

Frequently Asked Questions

What is clinical trial NCT01417195 about?

NCT01417195 is a clinical study titled "Menopur Mixed Protocol". The objective of this study was to compare the fertilization rate between the combination of Menopur and Bravelle mixed in the same syringe and Menopur alone, both administered subcutaneously (SC), in subjects undergoing Assisted Reproductive Technology (ART). Additionally the study assessed subject...

What is the current status of trial NCT01417195?

This trial is currently completed. It is a Phase 4 study. The enrollment target is 122 participants. The study started on 2011-07. Estimated completion is 2012-01.

What conditions does trial NCT01417195 study?

This clinical trial studies the following conditions: Infertility.

What interventions are being tested in trial NCT01417195?

The interventions under investigation include: Bravelle (DRUG), Menopur (DRUG).

Who is sponsoring clinical trial NCT01417195?

This trial is sponsored by Ferring Pharmaceuticals, which has 83 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT01417195 being conducted?

This trial has 10 study locations across Colorado, Florida, Georgia, Illinois, Maryland. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

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