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Klinefelter Syndrome and Testosterone Treatment in Puberty

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

Status
Recruiting
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06294990
Acronym
TiPY
Enrollment
32
Registered
2024-03-06
Start date
2024-08-15
Completion date
2029-12-31
Last updated
2025-02-19

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

Conditions

Klinefelter Syndrome

Keywords

Klinefelter syndrome, Puberty, Body composition

Brief summary

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.

Detailed description

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.

Interventions

DRUGTestosterone gel

Two years treatment with testosterone

OTHERPlacebo

Two years treatment with placebo

Sponsors

Lise Aksglæde
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
TRIPLE (Subject, Caregiver, Investigator)

Intervention model description

Multi-center, national, randomized, double-blind, placebo-controlled intervention study

Eligibility

Sex/Gender
MALE
Age
10 Years to 14 Years
Healthy volunteers
No

Inclusion criteria

* 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

Exclusion criteria

* 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

Design outcomes

Primary

MeasureTime frameDescription
Changes in body fat massBaseline and 1 and two yearsEvaluation of body fat percentage by whole body dual energy x-ray absorptiometry (DEXA) scan

Secondary

MeasureTime frameDescription
Pubertal development and viriliztionEvery three months for two yearsMeasurement of luteinizing hormone (LH) (IU/L) in serum
Pubertal developmentAt base line, and at 1 and 2 yearsMeasurement of the concentration of luteinizing hormone (LH) and follicle stimulating hormone (FSH) in the first, fasting, morning voiding. Measured in IU/L.
AnthropometryEvery three months for two yearsMeasurement of height (cm)
Bone healthAt baseline and at 1 and two yearsMeasurement of whole body bone mineral content (BMC) evaluated by whole body DXA scan
Measurement of bone turnover markersAt base line, and at 1 and 2 yearsMeasurement of 25-OH-vitamin D in blood sample
Changes in growthBase line and at 1 and 2 yearsEvaluation of bone age by X-ray of left hand and evaluated using the software BoneXpert version 3 (Hørsholm, Denmark)
Measurement of serum concentrations of growth factorsAt base line, and at 1 and 2 yearsMeasurement of IGF1, IGF2, IGF1BP-1-6 and acid-labile subunit (ALS)) (microg/L)
Muscle strengthEvery three months for two yearsMeasurement of standing jump length (cm)
Pubertal development and virilizationEvery three months for two yearsTanner genital (G) staging from G1 to G5. G1 is the prepubertal stage and G5 is the fully develloped stage.
Changes in markers of lipidsBase line and at 1 and 2 yearsMeasurement of cholesterol in blood sample
Changes in markers of metabolismBase line and at 1 and 2 yearsMeasurement of adiponectin in blood sample
Changes in markers of inflammationBase line and at 1 and 2 yearsMeasurement of CRP in blood sample
Neuropsychological evaluationBaseline and after two yearsThe Weschler Intelligence Scale for Children - Fifth Edition (WISC-V). The result is based on a combination of seperate index scores. A higher score generally indicates stronger cognitive abilities.
Cryopreservation of spermatozoaAfter 2 yearsIf the patient is able and willing he will have the possibility to deliver a semen sample for cryopreservation of potential spermatozoa
EpigeneticAt base line, and at 1 and 2 yearsThe effects on epigenetics will be evaluation by evaluating changes in DNA methylation patterns. This will be analyzed on DNA from white blood cells by applying Illumina methylation arrays.
Genetic effectsAt base line, and at 1 and 2 yearsDNA will be analyzed using a selected set of genetic polymorphisms in target genes with established or theoretic effects on hormone production and hormone receptor sensitivity. They will be analysed either by PCR genotyping or targeted sequencing (max. 200 selected genes). SNP arrays that exclusively target common variants, and not any rare variants, will be used to determine the influence of common genetic variation on the observed associations.
Small non-coding RNAAt base line, and at 1 and 2 yearsRNA analysis of circulating, small, non-coding RNA will be performed as a biomarker for the circulating concentrations of reproductive hormones and for overweight.
Changes i QTcBase line and at 1 and 2 yearsEvaluation of QT Interval with electrocardiogram (ECG)

Countries

Denmark

Contacts

Primary ContactLise Aksglaede, MD
lise.aksglaede@regionh.dk+45 35455064

Outcome results

None listed

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