- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01668056
Synchronization of Ovarian Stimulation for in Vitro Fertilization With Follicular Wave Emergence
The Role of Controlling Follicular Wave Emergence to Synchronize Ovarian Stimulation for in Vitro Fertilization
Ovarian stimulation is an important phase of in vitro fertilization (IVF) treatments. The harvest of a larger number of viable eggs per cycle compensate eventual laboratory difficulties and allow for the selection of embryos with higher implantation potential. In the current protocols, based on the most prevailing theory of ovarian follicular development, stimulation drugs are usually started on the second or third day after the beginning of menses. The follicular phase of the menstrual cycle is believed to be the only favorable moment for follicular development.
In the early 2000's a new model of human ovarian follicular development (follicular waves) has been proposed based on frequent transvaginal ultrasound observations between two ovulations. It has been shown that ovarian antral follicles develop in synchronous groups, two to three times in a cycle. In fact the follicular wave phenomenon has been initially described in the 80's on domestic animals, like the mare and the cow. Moreover, studies in these animals have shown that synchronizing the start of the ovarian stimulation drugs with the beginning of a follicular wave yields better results for assisted reproductive treatments. Consequently in ovarian stimulation protocols for animal assisted reproduction it is important to control the initiation of a follicular wave.
Current protocols of ovarian stimulation for IVF in women do not consider the start of a follicular wave to begin drug administration. Therefore the purpose of this study is to evaluate two methods to control the emergence of a follicular wave (ovulation induction and dominant follicle aspiration) and to investigate the effects of synchronizing ovarian stimulation for IVF with follicular wave emergence in women compared to one of the current stimulation protocols (flexible GnRH protocol).
Study Overview
Status
Conditions
Study Type
Enrollment (Anticipated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: Paulo HM Bianchi, MD
- Email: paulobianchi35@gmail.com
Study Locations
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Sao Paulo, Brazil
- Recruiting
- University of Sao Paulo General Hospital
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Contact:
- Paulo HM Bianchi, MD
- Email: paulobianchi35@gmail.com
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Principal Investigator:
- Paulo HM Bianchi, MD
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- age < 35 years old
- body mass index: 19-30 kg/m2
- tubal or male factor infertility with indication of in vitro fertilization
- antral follicle count: 10-20
- normal uterus in transvaginal ultrasound scan
- FSH on the third day of the menstrual cycle below 12mUI/mL and estradiol below 80pg/mL
- male partner with at least 5 million motile sperm and 1% normal strict morphology on semen analyses
Exclusion Criteria:
- ovarian factor infertility
- non identification of one or both ovaries in the transvaginal ultrasound scan
- non treated endocrine disorders
- smoking habit
- endometriosis stage III -IV
- severe male factor infertility (less than one million sperm per mL of semen)
Study Plan
How is the study designed?
Design Details
- Primary Purpose: TREATMENT
- Allocation: RANDOMIZED
- Interventional Model: PARALLEL
- Masking: NONE
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
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ACTIVE_COMPARATOR: Control
Patients will be stimulated according to the conventional flexible GnRH antagonist protocol for IVF.
Alfa follitropin (150IU a day) will be started on the third day of the menstrual cycle.
Treatment monitoring will be done with transvaginal ultrasound scans and serum determinations of estradiol and progesterone 5 days after the start of gonadotropins and every each day thereafter.
Once the leading follicle reaches 13 mm in mean diameter 0,25mg of cetrorelix acetate will be administered daily.
Once at least two follicles reach 18mm or more in mean diameter 250 micrograms of choriogonadotropin alfa will be administered and 36 hours latter patients will undergo follicle aspiration for IVF.
Embryos will be cryopreserved (vitrification) on the third or fifth day of development.
Two months after women will undergo uterine preparation for embryo transfer.
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Conventional flexible GnRH antagonist protocol of ovarian stimulation for in vitro fertilization, with gonadotropin star at the third day of a natural menstrual cycle.
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EXPERIMENTAL: Ovulation induction
Patients will be monitored with daily transvaginal ultrasound scans from the tenth day of the menstrual cycle on.
When the dominant follicle reaches a mean diameter of 16mm or more, patients will receive 250 micrograms of choriogonadotropin alfa subcutaneously.
Daily transvaginal ultrasound scans will be done starting two days after the administration of the medication until a cohort of ovarian follicles between 4-6 mm is seen (follicular wave emergence).
From this point on patients will undergo the same stimulation protocol as Controls, i.e., flexible GnRH antagonist protocol.
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Administration of 250 micrograms of choriogonadotropin alfa subcutaneously when the dominant follicle of a natural menstrual cycle reaches 16mm or more of mean diameter.
Verify if this intervention is able to induce follicular wave emergence and synchronize the start of the flexible GnRH antagonist protocol of ovarian stimulation with the start of a follicular wave.
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EXPERIMENTAL: Dominant follicle aspiration
Patients will be monitored with daily transvaginal ultrasound scans from the tenth day of the menstrual cycle on.
When the dominant follicle reaches a mean diameter of 16mm or more, patients will then undergo aspiration of the dominant and all follicles greater than 10mm in mean diameter.
aspiration will be transvaginal ultrasound guided and under sedation, as for oocyte retrieval.
Oocytes eventually obtained at this first aspiration will not be used for IVF.
Daily transvaginal ultrasound scans will be done starting the day after the follicular aspiration until a cohort of follicles between 4-6 mm is seen (follicular wave emergence).
From this point on patients will undergo the same stimulation protocol as Controls, i.e., flexible GnRH antagonist protocol.
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Aspiration of all follicles greater than 10mm in mean diameter when the dominant follicle of a natural menstrual cycle reaches 16mm or more of mean diameter.
Aspiration will be guided by transvaginal ultrasound.
Verify if this intervention is able to induce follicular wave emergence and synchronize the start of the flexible GnRH antagonist protocol of ovarian stimulation with the start of a follicular wave.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
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Emergence of an ovarian follicular wave after dominant follicle aspiration or hCG administration
Time Frame: One year
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Evaluate if the aspiration of the dominant follicle is able to induce a follicular wave to emerge. Evaluate if administration of hCG is able to induce ovulation of a dominant follicle larger than 16mm and to induce a follicular wave to emerge. A follicular wave emergence is defined as an increase in the number of ovarian follicles smaller than 10mm seen at the transvaginal ultrasound scan after the interventions |
One year
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Follicular growth pattern on ultrasound scan
Time Frame: One year
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Evaluate with periodic transvaginal ultrasound scan the size (mm), number and growth rate (mm/day) of ovarian follicles in each of the three groups
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One year
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Estradiol and progesterone levels during ovarian stimulation
Time Frame: One year
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Evaluate blood levels of estradiol (pg/mL) and progesterone (ng/mL) during ovarian stimulation in each of the three groups at each visit to evaluate the progress of treatment.
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One year
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Number of mature oocytes retrieved
Time Frame: One year
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Evaluate the number of metaphase II oocytes retrieved in each of the three groups
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One year
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Total dose of gonadotrophins used
Time Frame: One year
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Total dose of gonadotrophins (in international units) necessary to stimulate the ovaries (from the first day of stimulation until the last dose of recombinant FSH administered before the oocyte retrieval)
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One year
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Fertilization rate
Time Frame: One year
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Number of embryos formed in relation with the number of oocytes inseminated
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One year
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Pregnancy rate
Time Frame: One year
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Positive beta hCG determination on blood 10 days after embryo transfer
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One year
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Collaborators and Investigators
Investigators
- Study Chair: Edmund c Baracat, PhD, University of Sao Paulo Medical School
- Study Director: Paulo C Serafini, PhD, University of Sao Paulo Medical School
- Principal Investigator: Paulo HM Bianchi, MD, University of Sao Paulo Medical School
Publications and helpful links
General Publications
- Baerwald AR, Adams GP, Pierson RA. Characterization of ovarian follicular wave dynamics in women. Biol Reprod. 2003 Sep;69(3):1023-31. doi: 10.1095/biolreprod.103.017772. Epub 2003 May 14.
- Baerwald AR, Adams GP, Pierson RA. A new model for ovarian follicular development during the human menstrual cycle. Fertil Steril. 2003 Jul;80(1):116-22. doi: 10.1016/s0015-0282(03)00544-2.
- Baerwald AR, Adams GP, Pierson RA. Ovarian antral folliculogenesis during the human menstrual cycle: a review. Hum Reprod Update. 2012 Jan-Feb;18(1):73-91. doi: 10.1093/humupd/dmr039. Epub 2011 Nov 8.
- Adams GP, Singh J, Baerwald AR. Large animal models for the study of ovarian follicular dynamics in women. Theriogenology. 2012 Nov;78(8):1733-48. doi: 10.1016/j.theriogenology.2012.04.010. Epub 2012 May 22.
- de Mello Bianchi PH, Serafini P, Monteiro da Rocha A, Assad Hassun P, Alves da Motta EL, Sampaio Baruselli P, Chada Baracat E. Review: follicular waves in the human ovary: a new physiological paradigm for novel ovarian stimulation protocols. Reprod Sci. 2010 Dec;17(12):1067-76. doi: 10.1177/1933719110366483. Epub 2010 May 3.
- Bianchi PH, Viera LM, Gouveia GR, Rocha AM, Baruselli PS, Baracat EC, Serafini PC. Study of two strategies to induce follicular wave emergence for assisted reproductive treatments (ART)-a preliminary trial. J Assist Reprod Genet. 2015 Apr;32(4):543-9. doi: 10.1007/s10815-015-0432-3. Epub 2015 Feb 21.
Study record dates
Study Major Dates
Study Start
Primary Completion (ANTICIPATED)
Study Completion (ANTICIPATED)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (ESTIMATE)
Study Record Updates
Last Update Posted (ESTIMATE)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 1099/09
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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