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Идёт набор NCT06294990

Klinefelter Syndrome and Testosterone Treatment in Puberty

Фаза IV С лечением Klinefelter Syndrome

Ориентир для пациента и семьи

Простыми словами

Автоматическая сводка по структурированным данным реестра. Она помогает сориентироваться, но не заменяет официальный протокол или оценку врача.

Что изучают
В протоколе указаны: Testosterone gel, Placebo.
Кому может быть актуально
Состояния в реестре: Klinefelter Syndrome. Базовые параметры: 10 лет — 14 лет · Мужчины.
Что важно проверить
Возраст, диагноз и пол — только базовые ориентиры. Предыдущее лечение, анализы и другие обязательные условия указаны ниже в критериях участия.
Где проводится
Дания
Следующий шаг
Сохраните исследование, покажите его лечащему врачу и уточните актуальный статус у исследовательского центра. Расходы, документы и поездка →
Официальное название

Klinefelter Syndrome - the Effect of Testosterone Treatment in Puberty. a Randomized, Double-blind Placebo-controlled Intervention Study: 'The TiPY Study'

Обзор

The goal of this randomized clinical trial is to study the effect of testosterone replacement therapy during puberty in boys with Klinefelter syndrome (KS, 47,XXY). The main questions to answer are how treatment with testosterone will affect body fat mass, lipid and glucose metabolism, growth and body proportions, bone mineralization as well as effects on neurocognitive development and emotional and social difficulties. Participants will be randomized to two years treatment with testosterone or placebo.

Подробное описание

Klinefelter syndrome (KS, 47,XXY) is the most frequent sex chromosome disorder with a prevalence of 1:660 boys. Patients with KS are hypogonadal due to a progressive testicular destruction starting already in childhood. Consequently, the adult male with KS is characterized by small testes, signs of incomplete virilization (e.g. lack of voice deepening, sparse face and body hair, gynecomastia, low muscle mass, reduced penile length), hypergonadotropic hypogonadism, infertility and increased risk of metabolic syndrome, diabetes, cardiovascular disease, osteoporosis and psychosocial and neurodevelopmental challenges. Adults with KS have a poor health and a prevention of the major co-morbidities associated with KS and thereby an improvement in the general health would have an enormous impact on the life of a large cohort of males worldwide.

Sufficient testosterone is not only important in the adult but also during puberty and adolescence for a normal virilization and to improve body composition and body proportions, as well as to maximize peak bone mass acquisition. It has therefore been internationally accepted and makes biological sense to consider testosterone replacement therapy (TRT) during puberty in KS. However, there are no evidence based recommendations, and during recent years TRT in puberty has been questioned and is no longer recommended in some countries. There is a need on an international level for evaluating the effect of this treatment. We therefore aim at evaluating the effect of 2 years TRT during early puberty in boys with KS aged 10 to 14 years in this national, multi-center, randomized, double-blind, placebo-controlled intervention study. The primary endpoint is to evaluate the effect on body fat mass. The secondary endpoints are to evaluate effects on lipid and glucose metabolism, growth and body proportions, bone mineralization as well as effects on neurocognitive development and emotional and social difficulties.

Вмешательства

  • Препарат Testosterone gel
    Two years treatment with testosterone
  • Другое Placebo
    Two years treatment with placebo

Первичные конечные точки

  • Changes in body fat mass [Срок оценки: Baseline and 1 and two years]
Вторичные конечные точки (12)
  • Pubertal development and virilization [Срок оценки: Every three months for two years]
  • Pubertal development and virilization [Срок оценки: Every three months for two years]
  • Pubertal development and virilization [Срок оценки: Every three months for two years]
  • Pubertal development and virilization [Срок оценки: Every three months for two years]
  • Pubertal development and virilization [Срок оценки: Every three months for two years]
  • Pubertal development and viriliztion [Срок оценки: Every three months for two years]
  • Pubertal development and viriliztion [Срок оценки: Every three months for two years]
  • Pubertal development and viriliztion [Срок оценки: Every three months for two years]
  • Pubertal development and viriliztion [Срок оценки: Every three months for two years]
  • Pubertal development and viriliztion [Срок оценки: Every three months for two years]
  • Pubertal development and viriliztion [Срок оценки: Every three months for two years]
  • Pubertal development [Срок оценки: At base line, and at 1 and 2 years]

Критерии участия

Критерии включения

  • 47,XXY Klinefelter syndrome
  • Age 10-14 years at inclusion
  • Luteinizing Hormone > +2 standard deviations (SD) by ultrasensitive luteinizing hormone assay
  • Free Testosterone<+2 standard deviations
  • Signed consent from parents

Критерии исключения

  • Previous or ongoing T treatment except for TRT because of micropenis
  • Contraindications to testosterone treatment known hypersensitivity to testosterone or to any other constituent of the gel known or suspected prostatic cancer or breast carcinoma
  • Participation in any other clinical trial

Критерии приведены из реестра в оригинале (на английском). Окончательную оценку соответствия проводит исследовательский центр.

Здоровые добровольцы: Нет

Дизайн исследования

Распределение
Рандомизированное
Модель
Параллельные группы
Маскирование
Тройное слепое
Основная цель
Лечение

Центры проведения

Дания · 1 центр
  • Copenhagen University Hospital, Rigshospitalet — Copenhagen

Публикации

  • Caspersen ID, Fritzboger AFO, Petersen JH, Birkebaek N, Christensen AR, Schou AJ, Kristensen K, Ross JL, Davis S, Butler G, van Rijn S, Juul A, Aksglaede L. Effect of testosterone treatment during puberty in boys with Klinefelter syndrome (The TIPY Study): protocol for a nationwide randomised, double-blinded, placebo-controlled study. BMJ Open. 2025 Mar 15;15(3):e095628. doi: 10.1136/bmjopen-2024- PMID 40090688

Идентификаторы

NCT: NCT06294990 · 2023-505854-16-00

Первоисточники (государственные реестры)

Открыть это исследование на ClinicalTrials.gov ↗