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Higher estradiol dose may boost IVF success in frozen embryo transfers

NCT ID NCT07526207

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed This study
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

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.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Phase

Phase 4

Runs after approval, following long-term safety and how well the treatment works in everyday use.

Participants

850 people

The number who actually took part.

Started

Apr 2022

Finished

Feb 2026

Lead sponsor

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

18 to 40 years

Sex

Female participants only

Healthy volunteers

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

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

  • Cairo University

    Cairo, Al-Manial, 11956, Egypt

  • Kafrelsheikh University, faculty of medicine

    Kafr ash Shaykh, Kafr Elsheikh, 33516, Egypt

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