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NCT Number: NCT04167033

Ventricular Repolarization in Patients With Premature Ovarian Insufficiency (QTIOP)

Ventricular repolarization, measured by corrected QT interval (QTc), is influenced by sex hormones. A QTc above 460msec predisposes to the risk of "torsades-de-pointes"(TdP). The investigators have recently shown that estradiol determines an increase in QTc elongation and progesterone shortens it. In addition, high gonadotropin levels (FSH or LH) are associated with QTc prolongation. Hypergonadotropic hypogonadisms (low progesterone and high gonadotropins) are therefore hormonal situations that promote QTc prolongation. Premature ovarian insufficiency (POI) is one of them. Its management is based on the prescription of hormone replacement therapy (HRT). Epidemiological studies have shown that these patients would be at increased risk of cardiovascular mortality. Our team is interested in the effect of this pathological hormonal situation and its HRT on ventricular repolarization in order to define whether this is a population at risk for long QTc.

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Key information

About this study

Ventricular repolarization, measured by the duration of the heart rate corrected QT interval (QTc), is influenced by sex hormones. A QTc above 460msec predisposes to the risk of torsades-de-pointes (TdP); ventricular arrhythmias that can lead to sudden death.

From puberty to menopause, QTc is longer in women than in men (~10-15msec difference) and varies in women according to the menstrual cycle (~5-10msec). This explains the increased risk of TdP in women compared to men. During the menstrual cycle, the risk is highest for women during the follicular phase compared to the luteal phase. The investigators have recently shown that estradiol determines an increase in QTc elongation and progesterone shortens it. In addition, high gonadotropin levels (FSH or LH) are associated with QTc prolongation. Hypergonadotropic hypogonadisms (low progesterone and high gonadotropins) are therefore hormonal situations that promote QTc prolongation.

Premature ovarian insufficiency (POI) affects 1% of women under 40 years of age and is characterized by hypergonadotropic hypogonadism. POI is associated with hormonal deficiencies responsible for amenorrhea and infertility. Management is based on the prescription of hormone replacement therapy (HRT). Epidemiological studies have shown that these patients would be at increased risk of cardiovascular mortality. HRT will be based on the combination of an estrogen and a progestin and will lead to a variable decrease in gonadotropins, depending on the steroid hormones/doses used. Our team, after structuring one of the largest international cohorts of patients with POI, is interested in the effect of this pathological hormonal situation and its HRT on ventricular repolarization to define whether this is a population at risk for long QTc. Indeed, ECG follow-up is recommended and many drugs (cardiovascular or not), are to be avoided, or even contraindicated in situations at risk of long QTc.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

Patients with POI

  • Patient aged 18 to 41 years
  • Patient with POI diagnostic criteria (FSH >25UI/l twice at intervals of a few weeks) with amenorrhea
  • No hormone treatment interacting with the gonadotropic axis for at least one month before inclusion
  • Patient who has signed informed consent
  • Patient affiliated to a social security system

Healthy volunteers (including POI control group)

  • Healthy women, aged 18 to 40 years, age-matched (+/- 5 years), and by BMI class (BMI<18, 18-25, 25-30, 30-35, 35-40, >40) compared to women with BPI
  • Women with regular cycles of 26 to 32 days
  • Women who has signed an informed consent form
  • Patient affiliated to a social security system

Exclusion criteria

Patients with POI

  • Patient on HRT during the 1st evaluation
  • Pregnant or breastfeeding woman
  • Treatment regimen known to lengthen QT or act on ventricular repolarization
  • Cardiac history in particular cardiac rhythm disorder
  • Diabetes
  • Patient on AME (unless derogation from affiliation),
  • Severe renal insufficiency (MDRD <30ml/min/m²)

Healthy volunteers (including POI control group)

  • Diabetes or any chronic disease (including cardiovascular and endocrine)
  • Pregnant or breastfeeding woman
  • Hormonal contraceptive treatment in progress or stopped less than 3 months ago
  • Chronic treatment affecting the duration of QTc
  • Woman under AME (unless affiliation derogation)

Treatment and study plan

Hormone replacement therapy:effect on ventricular repolarization

Drug

Hormone replacement therapy and QTc measurement

ECG

Diagnostic Test

QTc measurement

Primary outcomes

  1. Duration of QTc

    Time frame: in the luteal phase between Day22 and Day25

    Compare the duration of QTc in patients with non-substituted POI with that of matched healthy volunteers on cardiovascular risk factors. The QTc will be measured by the Fridericia method

Secondary outcomes

  1. Duration of QTc

    Time frame: the day before and between Day22 and Day60 after the introduction of HRT

    Measure the duration of QTc in women with POI before and after the introduction of HRT

  2. Duration of QTc

    Time frame: in the luteal phase between Day22 and Day25

    Study the association between sex hormone levels (gonadotropins, steroid hormones) and QTc duration, as well as their variation in patients with POI and healthy volunteers

Study contacts

Contact information is provided by the study sponsor or research team.

Anne Bissery, MD

CONTACT

[email protected]

1 42 16 24 32 ext. +33

Fredy Pene, Mr

CONTACT

[email protected]

1 42 16 24 35 ext. +33

Sponsors and collaborators

Lead sponsor

Assistance Publique - Hôpitaux de Paris

Other

Registry information

Official study title

Study of Ventricular Repolarization in Patients With Premature Ovarian Insufficiency and Influence of Estrogen-progestin Replacement Therapy

Acronym: QTIOP

Important dates

Study start
2021
Primary completion
2027
Study completion
2027
First posted
Nov 18, 2019
Registry last updated
Dec 9, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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