Corifollitropin Alfa on D5 Versus D7 After Contraceptive Pill

See also
Status	Clinical Trial	Phase
Completed	`NCT01645241` - Evolutive Potential of Embryos Obtained From Oocytes After Luteal Phase Ovarian Stimulation	N/A
Completed	`NCT03668184` - What Are the Predictive Factors for Preeclampsia in Oocyte Recipients? - PREROVE
Terminated	`NCT03088735` - Transfer Strategy in an Oocyte Donation Programme	N/A
Recruiting	`NCT05521828` - Luteal Phase Ovarian Stimulation With Follitropin Delta and Dydrogesterone	N/A

See also

Status

Clinical Trial

Phase

Completed

NCT01645241 - Evolutive Potential of Embryos Obtained From Oocytes After Luteal Phase Ovarian Stimulation

N/A

Completed

NCT03668184 - What Are the Predictive Factors for Preeclampsia in Oocyte Recipients? - PREROVE

Terminated

NCT03088735 - Transfer Strategy in an Oocyte Donation Programme

N/A

Recruiting

NCT05521828 - Luteal Phase Ovarian Stimulation With Follitropin Delta and Dydrogesterone

N/A

Interventional studies are often prospective and are specifically tailored to evaluate direct impacts of treatment or preventive measures on disease.

Observational studies are often retrospective and are used to assess potential causation in exposure-outcome relationships and therefore influence preventive methods.

Expanded access is a means by which manufacturers make investigational new drugs available, under certain circumstances, to treat a patient(s) with a serious disease or condition who cannot participate in a controlled clinical trial.

Clinical trials are conducted in a series of steps, called phases - each phase is designed to answer a separate research question.

Phase 1: Researchers test a new drug or treatment in a small group of people for the first time to evaluate its safety, determine a safe dosage range, and identify side effects.
Phase 2: The drug or treatment is given to a larger group of people to see if it is effective and to further evaluate its safety.
Phase 3: The drug or treatment is given to large groups of people to confirm its effectiveness, monitor side effects, compare it to commonly used treatments, and collect information that will allow the drug or treatment to be used safely.
Phase 4: Studies are done after the drug or treatment has been marketed to gather information on the drug's effect in various populations and any side effects associated with long-term use.

NCT number	NCT02490150
Study type	Interventional
Source	Institut Universitari Dexeus
Contact
Status	Completed
Phase	Phase 4
Start date	February 2015
Completion date	June 2016

Corifollitropin Alfa on D5 Versus D7 After Contraceptive Pill

Clinical Trial Summary

Clinical Trial Description

Study Design

Related Conditions & MeSH terms