Study of Follicle Stimulating Hormone (FSH) Receptor in Women With Low Antral Follicle Count
This study has been completed.
Sponsor:
Assistance Publique - Hôpitaux de Paris
Information provided by:
Assistance Publique - Hôpitaux de Paris
ClinicalTrials.gov Identifier:
NCT00231504
First received: October 3, 2005
Last updated: January 5, 2010
Last verified: March 2007
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Purpose
The deficit in the total number of antral follicles is associated with a reduction of the ovarian fertility potential in young women.
The principal objective of this study is to evaluate the relationship between FSH receptor polymorphism and antral follicle count.
The investigators have designed a study of FSH receptor polymorphisms P1 and P2 as an association with a low antral follicle count in the ovary.
| Condition | Intervention | Phase |
|---|---|---|
|
Antral Follicle Deficit Fertility |
Procedure: Blood samples |
Phase 1 |
| Study Type: | Observational |
| Study Design: | Observational Model: Cohort Time Perspective: Prospective |
| Official Title: | Study of Follicle Stimulating Hormone (FSH) Receptor in Women With Low Antral Follicle Count |
Resource links provided by NLM:
Further study details as provided by Assistance Publique - Hôpitaux de Paris:
Biospecimen Retention: Samples With DNA
DNA
| Enrollment: | 82 |
| Study Start Date: | October 2005 |
| Study Completion Date: | May 2009 |
| Primary Completion Date: | March 2009 (Final data collection date for primary outcome measure) |
Intervention Details:
Detailed Description:
-
Procedure: Blood samples
Blood samples
Other Name: Blood samples
The present study will compare the prevalence of FSH receptor polymorphisms P1 and P2 in women having reduced follicle count (1 to 9 antral follicles) or normal follicle count (13 to 20 antral follicles) determined by ultrasound scans.
Eligibility| Ages Eligible for Study: | 18 Years to 35 Years |
| Genders Eligible for Study: | Female |
| Accepts Healthy Volunteers: | Yes |
| Sampling Method: | Non-Probability Sample |
Study Population
YOUNG WOMAN
Criteria
Inclusion Criteria:
- 18 to 35 years old
- 1 to 9 or 13 to 20 antral follicles
- Caucasian, occidental Europe
- Presence of both ovaries
- Informed consent
Exclusion Criteria:
- Ovarian anomalies
- Menopause
- Pregnancy
- Other diseases
Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00231504
Locations
| France | |
| Antoine Beclere Hospital, Obstetrics and Gynaecology and Reproduction Medicine Service | |
| Paris, France, 92140 | |
Sponsors and Collaborators
Assistance Publique - Hôpitaux de Paris
Investigators
| Principal Investigator: | Renato FANCHIN, MD | Assistance Publique - Hôpitaux de Paris |
More Information
No publications provided
| Responsible Party: | Christophe Aucan, Department Clinical Rechearch of Developpement |
| ClinicalTrials.gov Identifier: | NCT00231504 History of Changes |
| Other Study ID Numbers: | P041013, CRC04140 |
| Study First Received: | October 3, 2005 |
| Last Updated: | January 5, 2010 |
| Health Authority: | France: Ministry of Health |
Keywords provided by Assistance Publique - Hôpitaux de Paris:
|
Polymorphism P1 Polymorphism P2 FSH Receptor Antral follicle count FSH receptor polymorphism |
Additional relevant MeSH terms:
|
Infertility Genital Diseases, Male Genital Diseases, Female Follicle Stimulating Hormone |
Hormones Hormones, Hormone Substitutes, and Hormone Antagonists Physiological Effects of Drugs Pharmacologic Actions |
ClinicalTrials.gov processed this record on May 21, 2013