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Impact of Follicular and Blood G-CSF on Pregnancy and Implantation Rate During Modified Natural in Vitro Fertility Cycle (G-CSF FIVnat)

This study is currently recruiting participants.
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Verified July 2017 by OVO R & D
Information provided by (Responsible Party):
OVO R & D Identifier:
First received: June 19, 2012
Last updated: July 24, 2017
Last verified: July 2017
Recently, scientists look into G-CSF (Granulocyte - Colony Stimulatin Factor). The use of this molecule is increasing in reproduction pathology. High level of follicular and blood G-CSF on the day of oocyte retrieval could correlate with higher pregnancy and implantation rates.

Condition Intervention
Infertility Procedure: Blood test

Study Type: Observational
Study Design: Observational Model: Case-Only
Time Perspective: Prospective
Official Title: Impact of Follicular and Blood G-CSF on Pregnangcy and Implantation Rate During Modified Natural in Vitro Fertility Cycle

Further study details as provided by OVO R & D:

Primary Outcome Measures:
  • Serum and / or follicular minimum level of G-CSF predictive of pregnancy [ Time Frame: 6 months ]

Biospecimen Retention:   Samples Without DNA
Serum sample Follicular fluid

Estimated Enrollment: 224
Study Start Date: March 2012
Estimated Study Completion Date: January 2020
Estimated Primary Completion Date: January 2020 (Final data collection date for primary outcome measure)
Groups/Cohorts Assigned Interventions
Patient following a natural In Vitro Fecondation cycle
Procedure: Blood test

Taking blood sample of the patient during the day 3, triggering day, oocyte collection day and pregnancy test day.

Taking the follicular fluid during the oocyte collection day


Ages Eligible for Study:   18 Years to 43 Years   (Adult)
Sexes Eligible for Study:   Female
Accepts Healthy Volunteers:   No
Sampling Method:   Probability Sample
Study Population
Women with a natural cycle of an In Vitro Fecondation

Inclusion Criteria:

  • Women between 18 and 43 years old
  • Women natural In Vitro Fecondation

Exclusion Criteria:

  • No exclusion criteria
  Contacts and Locations
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its identifier: NCT01668225

Contact: Cynthia Levesque (514) 798-2000 ext 755
Contact: Michael Harnois (514) 798-2000 ext 755

Canada, Quebec
Ovo Fertilité Recruiting
Montréal, Quebec, Canada, J4P 2S4
Contact: Shirley Brugerie, Director    (514) 798-2000 ext 753   
Contact: Cynthia Levesque, Research assistant    514-798-2000 ext 755   
Sponsors and Collaborators
Principal Investigator: Pierre Lehmann, MD Clinique ovo
  More Information

Responsible Party: OVO R & D Identifier: NCT01668225     History of Changes
Other Study ID Numbers: OVO-11-02
Study First Received: June 19, 2012
Last Updated: July 24, 2017

Additional relevant MeSH terms:
Genital Diseases, Male
Genital Diseases, Female processed this record on August 22, 2017