Skip to content

Impact of Supraphysiological Estradiol on ECG in IVF Patients

Impact of Supraphysiological Estradiol Levels on Cardiac Electrophysiological Parameters During IVF: A Prospective Observational Study

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07007416
Enrollment
62
Registered
2025-06-05
Start date
2024-12-15
Completion date
2025-01-31
Last updated
2025-06-05

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

Conditions

Cardiac Electrophysiology, Electrocardiography (ECG), Estradiol, In Vitro Fertilization, Reproductive Endocrinology

Brief summary

This prospective observational study aimed to evaluate the effects of supraphysiological estradiol (E2) levels, induced by gonadotropin therapy during IVF, on cardiac electrophysiological parameters. Sixty-two women aged 18-40 undergoing IVF treatment at Konya City Hospital between December 2024 and January 2025 were included. ECG recordings were performed twice: once before gonadotropin stimulation and again on the day of hCG administration, when peak E2 levels were expected. Routine blood tests and hormone levels were also evaluated. Patients with obesity, cardiovascular disease, chronic illness, or medication use were excluded. After treatment, significant increases were observed in PR interval, J-Tpeak, QTc, and Tp-e values. E2 changes showed a moderate negative correlation with QTc and a low positive correlation with J-Tpeak. The results suggest that elevated E2 levels during IVF may affect cardiac electrophysiology, highlighting the need for careful monitoring in women with cardiac risk factors.

Interventions

None listed

Sponsors

Konya City Hospital
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 40 Years

Inclusion criteria

* Female patients aged 18 to 40 years Undergoing IVF treatment at Konya City Hospital between December 2024 and January 2025 No cardiac pathology based on cardiology consultation Eligible for controlled ovarian stimulation using a short antagonist protocol Provided informed consent

Exclusion criteria

\- Age under 18 or over 40 years Baseline estradiol level \> 50 ng/L on day 2 of menstrual cycle Presence of any known chronic diseases (e.g., diabetes mellitus, hypertension, rheumatologic disorders, thyroid disorders) Use of any medications other than those used for IVF Current smoker or alcohol user Family history of cardiac disease or sudden cardiac death Personal history of myocardial infarction, angina, heart failure, or any structural heart disease History of cardiac surgery or coronary intervention

Design outcomes

Primary

MeasureTime frameDescription
Change in QTc Interval Before and After Gonadotropin-Induced Estradiol ElevationApproximately 8-12 days from baseline to post-treatment ECGQTc interval will be measured via 12-lead electrocardiography (ECG) at two timepoints: (1) on menstrual cycle day 2-3 prior to gonadotropin stimulation (baseline), and (2) on the day of hCG administration when estradiol reaches peak levels. The difference between pre- and post-treatment QTc values will be calculated.

Secondary

MeasureTime frameDescription
Change in PR Interval Following Gonadotropin-Induced Estradiol ElevationApproximately 8-12 daysPR interval will be assessed using standard 12-lead ECG both before and after gonadotropin stimulation. Measurements will be taken on menstrual day 2-3 and again on the day of hCG administration to evaluate PR interval prolongation in response to elevated estradiol levels.

Countries

Turkey (Türkiye)

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 22, 2026