Skip to content

The Influence of Estradiol Supplementation During the Luteal in Patients Undergoing IVF Treatment

Blinded Randomised Trial About the Influence of Estradiol Supplementation During the Luteal in Patients Undergoing in Vitro Fertilization (IVF) Treatment

Status
UNKNOWN
Phases
Phase 1
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00490308
Enrollment
120
Registered
2007-06-22
Start date
2007-08-31
Completion date
2008-08-31
Last updated
2007-06-26

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Infertility

Keywords

luteal, phase, estradiol, pregnancy, rate

Brief summary

To evaluate whether treatment with Estradiol supplementation during the luteal phase improves IVF outcomes Patients undergoing IVF treatment with controlled ovarian hyperstimulation using a GnRH analog will receive 4 mg estradiol valerate in the luteal phase.Patient's followup will include E2 progesterone and BHCG 14 days after embryo transfer and vaginal ultrasound on day 21 and 28 after embryo transfer

Detailed description

The study will include Patients undergoing IVF treatment with controlled ovarian hyperstimulation using a daily GnRH analog in a long protocol,older then 18, .The women will be randomised to two groups.Both groups will be given vaginal tabs of natural micronized progesterone(Uterogestan) The study group will be given oral estradiol Valerate 4 mg.Prior to treatment, each patient will be signed on informed concent. Patients will be excluded if they are older than 40, have any systemic illnesses or a personal or family history of a thromboembolic event. Follow up: Verification of pregnancy status and hormonal profile will be carried out on day fourteen after embryo transfer by means of serum hCG,P and E2. clinical pregnancy will be defined as the presence of a gestational sac on ultrasonography on day 21 after embryo transfer and fetal heart will be evaluated on day 28

Interventions

DRUGTreatment with estradiol valerate

Sponsors

Assaf-Harofeh Medical Center
Lead SponsorOTHER_GOV

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 40 Years
Healthy volunteers
Yes

Inclusion criteria

* Women treated for infertility with controlled ovarian hyperstimulation using daily GnRH agonist

Exclusion criteria

* Women younger then 18 or older then 40 * Women with systemic disease * Women with a family or personal history of thromboembolic event

Design outcomes

Secondary

MeasureTime frame
E2 and progesterone levels

Countries

Israel

Contacts

Primary ContactRan Svirsky, MD
rsvirs@gmail.com+972-0523-859521

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026