Effects of Clomiphene Citrate Ovulation Induction on Frozen Embryo Transfer

Sponsor
ShangHai Ji Ai Genetics & IVF Institute (Other)
Overall Status
Unknown status
CT.gov ID
NCT03309436
Collaborator
(none)
360
1
2
10.7
33.5

Study Details

Study Description

Brief Summary

Clomiphene citrate has been widely used for treatment of infertility for decades. Although its anti-estrogenic effects leads to low pregnancy rate, clomiphene citrate is still a first-line treatment for ovulation induction because of its simple usage, low prices, no injection and low risk of ovarian hyperstimulation syndrome. Clomiphene citrate shows high affinity with estrogen receptor, which inhibits endometrial proliferation, inevitably leads to a decline in endometrial receptivity, thus affecting the success rate of IVF.

In that case, use clomiphene citrate for ovulation induction is lost more than gained based on fresh embryo transfer. But recently, some researchers have proposed to extend the time from ovulation induction to embryo transfer, and the increased level of estradiol can replace clomiphene citrate to combine with the receptor, so that the uterine environment is more conducive to pregnancy. Therefore, use clomiphene citrate based on vitrification of embryo maybe a good way for treatment of infertility.

At present, using frozen embryo transplantation after ovulation induction by clomiphene citrate is a common treatment, but few research has mentioned the best time for embryo implantation. The investigators research is to find the most appropriate time for frozen embryo implantation after using clomiphene citrate for ovulation induction.

Condition or Disease Intervention/Treatment Phase
  • Drug: Clomiphene Citrate protocol
  • Procedure: Procedure
Phase 4

Detailed Description

This study receives patients from 2017 August to 2018 June who undergo ART treatment at Shanghai Jiai Genetics & IVF Institute and taken either CC or GnRH antagonist protocol(control group) for ovulation induction.

The investigators will record every patients' age, BMI, serum E2, P, LH level, infertility factors and pregnancy outcomes, counted the implantation rate and clinical pregnancy rate, and then used SPSS Software x2 test for statistical analysis, the significance was set at p<0.05.The investigators will also make a correlation analysis about the serum hormone level and pregnancy outcomes.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
360 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Single (Care Provider)
Primary Purpose:
Treatment
Official Title:
Effects of Clomiphene Citrate Ovulation Induction on Frozen Embryo Transfer
Actual Study Start Date :
Aug 7, 2017
Anticipated Primary Completion Date :
Jun 30, 2018
Anticipated Study Completion Date :
Jun 30, 2018

Arms and Interventions

Arm Intervention/Treatment
Experimental: Use Clomiphene Citrate protocol

Ovulation induction: regular Clomiphene Citrate protocol. Start use rFSH or HMG from day 2/3 of the menstrual cycle, the initial dosage is determined by patients' age, BMI, antral follicle number, FSH, E2, AMH and past ovarian response, usually 150-225IU/d, until hCG injection. At the same time, take CC 100mg/d until hCG injection. The dosage of Gn will be adjust by serum E2, P, LH and the development of follicular.

Drug: Clomiphene Citrate protocol
Take CC 100mg/d at the same time with Gn until hCG injection.
Other Names:
  • CC
  • Active Comparator: Procedure

    Ovulation induction: regular GnRH antagonist protocol. Start use rFSH or HMG from day 2/3 of the menstrual cycle, the initial dosage is determined by patients' age, BMI, antral follicle number, FSH, E2, AMH and past ovarian response, usually 150-225IU/d, until hCG injection. When a dominant follicle diameter over 14mm or serum E2 over 350pg/ml, use GnRH-ant 0.25mg/d, until hCG injection. The dosage of Gn will be adjust by serum E2, P, LH and the development of follicular.

    Procedure: Procedure
    When a dominant follicle diameter over 14mm or serum E2 over 350pg/ml, use GnRH-ant 0.25mg/d, until hCG injection.
    Other Names:
  • GnRH antagonist protocol
  • Outcome Measures

    Primary Outcome Measures

    1. Clinical pregnancy [4 weeks after embryo transfer for the patient]

      Clinical pregnancy is defined as the presence of a gestational sac confirmed by transvaginal ultrasound examination. Clinical pregnancy rate per treatment cycle will also be calculated based on ITT.

    Secondary Outcome Measures

    1. Ongoing pregnancy [12 weeks after embryo transfer for the patient]

      Ongoing pregnancy is defined as a viable intrauterine pregnancy after 12 weeks of embryo transfer. Ongoing pregnancy rate per treatment cycle will also be calculated on intend-to-treat(ITT) basis.

    2. Implantation of transferred embryo [2 weeks after embryo transfer for the patient]

      Implantation rate per embryo transferred will also be calculated.

    Other Outcome Measures

    1. Regression analysis 1 [12 weeks after embryo transfer for the patient]

      Regression analysis about the pregnancy outcomes and patients' serum E2,P4,LH levels on the day of hCG injection

    2. Regression analysis 2 [12 weeks after embryo transfer for the patient]

      Regression analysis about the pregnancy outcomes and patients' serum E2,P4,LH levels on the day of embryo transfer

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years to 40 Years
    Sexes Eligible for Study:
    Female
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:

    Women 18-40 years of age who are scheduled for IVF or ICSI in our IVF institute while meeting the following criteria:

    1. AMH ≥ 2;

    2. Infertility factors: tubal factor, severe oligospermia, etc;

    3. FET cycle;

    4. Cleavage stage embryo transfer (Day 3).

    Exclusion Criteria:
    1. BMI ≤ 18.4 or ≥ 25.0;

    2. Have pregnancy complications;

    3. Genital tract malformations, uterine cavity diseases, PCOS;

    4. Endometriosis;

    5. Genetic diseases, severe somatic diseases, mental disorder.

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Shanghai Jiai Genetics & IVF Institute Shanghai China 200011

    Sponsors and Collaborators

    • ShangHai Ji Ai Genetics & IVF Institute

    Investigators

    • Study Chair: XIAOXI SUN, MD, Shanghai Jiai Genetics & IVF Institute

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    ShangHai Ji Ai Genetics & IVF Institute
    ClinicalTrials.gov Identifier:
    NCT03309436
    Other Study ID Numbers:
    • JIAI E2017-11
    First Posted:
    Oct 13, 2017
    Last Update Posted:
    Oct 13, 2017
    Last Verified:
    Aug 1, 2017
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Product Manufactured in and Exported from the U.S.:
    No
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Oct 13, 2017