Higher estradiol dose may boost IVF success in frozen embryo transfers
NCT ID NCT07526207
First seen Jun 27, 2026 · Last updated Aug 14, 2026 · Updated 2 times
Summary
This study looked at whether taking 12 mg of estradiol daily is better than 8 mg for preparing the uterus lining in women undergoing frozen embryo transfer. 850 women aged 18-40 were randomly assigned to one of the two doses. The goal was to see if the higher dose leads to more pregnancies. The trial is complete and results will help doctors choose the best dose for IVF patients.
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Study facts
What this study's own registry entry says, in plain language.
- Phase
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Phase 4
Runs after approval, following long-term safety and how well the treatment works in everyday use.
- Participants
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850 people
The number who actually took part.
- Started
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Apr 2022
- Finished
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Feb 2026
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 to 40 years
- Sex
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Female participants only
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
* Inclusion Criteria * Women aged 18-40 years. * Body mass index \<30 kg/m². * First autologous programmed HRT-FET cycle. * Endometrial preparation planned using oral estradiol valerate only. * Vitrified embryos derived from a previous autologous IVF or ICSI cycle. * Planned transfer of vitrified-warmed day-5 blastocyst(s). * Normal uterine cavity documented within the preceding 12 months. * Baseline transvaginal ultrasonography on cycle day 2 or 3 showing no ovarian cyst, dominant follicle, or intracavitary pathology. * Ability and willingness to provide written informed consent. * Ovulatory-factor infertility, including polycystic ovary syndrome, will be eligible provided all other criteria are fulfilled. * Exclusion Criteria * Contraindication to estrogen treatment * History of breast cancer or endometrial cancer * History of deep venous thrombosis, pulmonary embolism, or stroke * Allergy to the study medication * Irregular vaginal bleeding * Thyroid disorder * Hyperprolactinemia * Uncontrolled diabetes mellitus * Uncontrolled hypertension * Significant liver disease * Significant kidney disease * Severe systemic illness * Uterine abnormality * Untreated hydrosalpinx * Untreated pathology inside the uterine cavity * Donor-oocyte cycle * Donor-embryo cycle * Gestational-carrier cycle * Preimplantation genetic testing for aneuploidy (PGT-A) cycle * Natural cycle or modified natural cycle for endometrial preparation * Use of transdermal, vaginal, or mixed estrogen regimens * Use of letrozole, gonadotropins, or GnRH agonists for endometrial preparation * Premature ovarian insufficiency * Stage III or IV endometriosis * Recurrent implantation failure * Recurrent miscarriage * Abnormal parental karyotype * Active smoking * Difficult embryo transfer * Refusal to participate
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Cairo University
Cairo, Al-Manial, 11956, Egypt
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Kafrelsheikh University, faculty of medicine
Kafr ash Shaykh, Kafr Elsheikh, 33516, Egypt
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