Current partner codePEPTIDESDE
NCT01385332·Not applicable·INTERVENTIONAL

A Comparative Study of Two Patterns of Controlled Ovarian Hyperstimulation in Mid Follicular Phase or Early Luteal Phase for Egg Donors

Status

Completed

Phase

Not applicable

Enrollment

10

Locations

1

Results

Not posted

Publications

0

Study summary

What the protocol is testing.

The purpose of this study is to determine the efficacy and safety of two new patterns of controlled ovarian hyperstimulation (defined as total number of picked up eggs). This study will be performed in egg donors but these new patterns will be implemented in fertility preservation patients.

Interventions

Treatment arms and agents.

PROCEDURE

Early luteal phase

We will administer in the tenth day of the cycle 0.25mg/day of ganirelix until the estradiol levels will be less than 60pgr/mL. Then, we'll start a standard protocol of controlled ovarian hyperstimulation beginning with 150 UI/day. At 6th day of stimulation we'll begin with the antagonist.

PROCEDURE

Late follicular phase -COH-

We will administer in the 20th day of the cycle 0.25mg/day of ganirelix until the estradiol levels will be less than 60pgr/mL. Then, we'll start a standard protocol of controlled ovarian hyperstimulation beginning with 150 UI/day. At 6th day of stimulation we'll begin with the antagonist.

Timeline

From registration to results.

  1. First posted

    Jun 30, 2011

  2. Study start

    Mar 2010

  3. Primary completion

    Jun 2012

  4. Study completion

    Sep 2012

  5. Results posted

    Not reported

  6. Registry updated

    Sep 20, 2017

Outcomes

What the study measures.

Primary outcomes

Number of eggs

Time frame · Participants will be followed after 1-3 hrs of follicular aspiration.

The results will be presented in one year, egg recipients will be followed until 12 weeks of pregnancy.

Secondary outcomes

Not reported in the indexed record.

Eligibility

Who can take part.

Minimum age
18 Years
Maximum age
30 Years
Sex
FEMALE
Healthy volunteers
Yes

Inclusion Criteria: * premenopausal women 18-30 years old, with FSH levels \< 10mIU * irregular menstrual cycle * BMI between 12-28 * signed inform consent Exclusion Criteria: * Polycystic ovarian syndrome, gonadotropins allergy

Study locations

1 registered sites.

Spain. Showing up to 24 locations stored in the fast local snapshot.

Servei de Ginecologia i Obstetricia, Hospital del Mar-Parc Salut Mar

Barcelona, Spain

Publications

Results and literature.

No PMID-linked publications were present in this registry snapshot.

Primary links

Continue at the source.

Related trials

More studies on Ganirelix.

Related PeptideStat pages

Put the record in context.

Research pages describe evidence. Vendor pages, where available, describe independently tracked research-product listings and are not clinical recommendations.