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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05334888
Other study ID # ChariteU - ECRC XCVD
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date August 29, 2022
Est. completion date December 31, 2027

Study information

Verified date February 2024
Source Charite University, Berlin, Germany
Contact Sofia Forslund, Prof. Dr.
Phone +49 30 450540649
Email sofia.forslund@mdc-berlin.de
Is FDA regulated No
Health authority
Study type Observational [Patient Registry]

Clinical Trial Summary

The XCVD study investigates the influence of sex hormones on the composition of the gut microbiome and the possible emergence of cardiovascular risk factors. It will follow 200 healthy transgender individuals for two years during their hormone replacement therapy (HRT) and analyze them for the possible emergence of cardiovascular risk factors in relation to changes in the gut microbiome, metabolome, and immunome. We would also like to phenotype cardiovascular disease.


Description:

Conducting this innovative study using established scientific methods such as omics platforms, systems biology, and careful CVD phenotyping will allow, for the first time, extensive data collection on the influence of sex hormones on the development of CVD risk factors as well as the role of the gut microbiome. In doing so, the influence of circulating sex hormones can also be quantified to potentially predict CVD risk markers.


Recruitment information / eligibility

Status Recruiting
Enrollment 200
Est. completion date December 31, 2027
Est. primary completion date December 31, 2025
Accepts healthy volunteers
Gender All
Age group 18 Years to 50 Years
Eligibility Inclusion Criteria: - Age 18-50 - Language requirements: German, English - Previous gender hormone replacement therapy (HRT). - Ability to give consent and written consent to participate. - Health insurance (for clarification of incidental findings) Exclusion Criteria: - Diseases or functional disorders that, in the opinion of the study physician, preclude participation in the study. - Incapacity or other circumstances that do not allow study participants to fully understand the nature, significance and scope of this study.

Study Design


Locations

Country Name City State
Germany Experimental and Clinical Research Center, Clinical Research Unit Berlin

Sponsors (2)

Lead Sponsor Collaborator
Charite University, Berlin, Germany Deutsches Zentrum für Herz-Kreislauf-Forschung (DZHK)

Country where clinical trial is conducted

Germany, 

References & Publications (2)

Fromentin S, Forslund SK, Chechi K, Aron-Wisnewsky J, Chakaroun R, Nielsen T, Tremaroli V, Ji B, Prifti E, Myridakis A, Chilloux J, Andrikopoulos P, Fan Y, Olanipekun MT, Alves R, Adiouch S, Bar N, Talmor-Barkan Y, Belda E, Caesar R, Coelho LP, Falony G, — View Citation

Talmor-Barkan Y, Bar N, Shaul AA, Shahaf N, Godneva A, Bussi Y, Lotan-Pompan M, Weinberger A, Shechter A, Chezar-Azerrad C, Arow Z, Hammer Y, Chechi K, Forslund SK, Fromentin S, Dumas ME, Ehrlich SD, Pedersen O, Kornowski R, Segal E. Metabolomic and micro — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Changes in relative species abundance of intestinal bacteria compared baseline and 2 years after initiation of hormone replacement therapy. stool samples: Analysis with 16s rRNA sequencing Baseline, 2 years Follow Up (optional: after 1 year Follow Up)
Secondary Changes in cardio marker sera: following cardio marker can be determined by Electro Chemiluminescence Immuno-Assay: BNP and hs-troponin. Baseline, 2 years Follow Up (optional: after 1 year Follow Up)
Secondary Changes in hormone parameters sera: following hormones can be determined by mass spectrometry: Free Androgen Index (fAI), Beta-CrossLaps (BCTX), Carboxy-terminal Propeptide of Procollagen I (P1CP), Luteinizing Hormone, Oestradiol, Progesterone, Testosterone, Free Testosterone, Sex Hormone Binding Globulin, Dihydrotestosterone, Oestron, Free Oestriol. Baseline, 2 years Follow Up (optional: after 1 year Follow Up)
Secondary Changes in immune marker sera: pro- and anti-inflammatory cytokines using cytokine - multiplex panel and Immune cell populations with shotgun sequencing Baseline, 2 years Follow Up (optional: after 1 year Follow Up)
Secondary Changes in the concentration of of cortisol, progesterone, testosterone and dehydroepiandrosterone Hair sample: Hair steroid analysis with Immunoassay and LC-MS/MS Baseline, 2 years Follow Up
Secondary Changes in the oral species abundance saliva sample / oral / mouth: species abundance of oral bacteria (sequencing) Baseline, 2 years Follow Up (optional: after 1 year Follow Up)
Secondary Changes in Immune cell marker / regulatory T-cells Whole blood samples for Immune cell populations and peripheral blood mononuclear cells RNA isolation for whole-transcriptome shotgun sequencing. Baseline, 2 years Follow Up (optional: after 1 year Follow Up)
Secondary Changes in Epigenomics Whole blood samples for Immune cell populations and peripheral blood mononuclear cells RNA isolation for whole-transcriptome shotgun sequencing. Baseline, 2 years Follow Up (optional: after 1 year Follow Up)
Secondary Changes in Proteomics sera: MS and ELISA Baseline, 2 years Follow Up (optional: after 1 year Follow Up)
Secondary Changes in Metabolomics sera: MS and ELISA Baseline, 2 years Follow Up (optional: after 1 year Follow Up)
Secondary Changes in relative species abundance of skin microbioma skin swab: DNA - sequencing Baseline, 2 years Follow Up (optional: after 1 year Follow Up)
Secondary Changes in BMI body mass index (kg/m²) Baseline, 2 years Follow Up (optional: after 1 year Follow Up)
Secondary Changes in circumference circumference measurement (cm): waist and hip Baseline, 2 years Follow Up (optional: after 1 year Follow Up)
Secondary Gender identity questionnaire: Transgender Congruence Scale (TCS) & gender dysphoria Baseline, 6, 12, 18 and 24 months Follow Up
Secondary Changes in physical activity questionnaire: International Physical Activity Questionnaire / IPAQ Baseline, 6, 12, 18 and 24 months Follow Up
Secondary Changes in mental health questionnaire: Generalized Anxiety Disorder / GAD-7 Baseline, 6, 12, 18 and 24 months Follow Up
Secondary Changes in Perceived Stress questionnaire: Perceived Stress Questionnaire / PSQ Baseline, 6, 12, 18 and 24 months Follow Up
Secondary Changes in quality of life questionnaire: quality of life / PROMIS Baseline, 6, 12, 18 and 24 months Follow Up
Secondary Changes in depression questionnaire: Beck-Depressions-Inventar Revision / BDI II & The Patient Health Questionnaire (PHQ-9) Baseline, 6, 12, 18 and 24 months Follow Up
Secondary Changes in chrono type / sleep-wake behaviour questionnaire: Munich ChronoType Questionnaire (MCTQ) Baseline, 6, 12, 18 and 24 months Follow Up
Secondary Changes in dietary habits Food Frequency Quenstionnaire /FFQ, special diet and intake of dietary supplements, prebiotics and probiotics Baseline, 6, 12, 18 and 24 months Follow Up
Secondary Changes in socio-demographics Family status, education level, current working status, and living situation Baseline, 2 years Follow Up
Secondary Documentation of HRT HRT medication, dosing, regimes, and progress as well as all transition -relevant surgery and physical changes Baseline - HRT start, 6, 12, 18 and 24 months Follow Up
Secondary Changes in vital signs Systolic and diastolic blood pressure and heart rate Baseline, 2 years Follow Up (optional: after 1 year Follow Up)
Secondary Changes in life style risk parameters Smoking status, alcohol consumption and use of recreational drugs Baseline, 2 years Follow Up
Secondary Changes in CVD risk scores Framingham risk scores (FRS) and Systematic Coronary Risk Evaluation (SCORE) Baseline, 2 years Follow Up (optional: after 1 year Follow Up)
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