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Kidney DiseaseTRANSFORMNCT07542964

Transgender Analysis of Nephrological Studies Focused on Renal Metrics

An observational study of Kidney Disease and Kidney Injury, run by Amsterdam UMC, location VUmc at 1 site in Netherlands.

Not yet recruiting

Opening soon. The study is approved but enrolment has not started yet. Sites may already take enquiries.

Sites and contacts
Official record
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Trial summary

This study investigates how sex hormones affect kidney function in people undergoing gender-affirming hormone therapy (GAHT). We know men have a faster progression of kidney disease. Read more about this study

Who is it for?
Ages 18 to 40 years
What is being tested?
P-aminohippurate clearance study, Iohexol infusion and Hyperinsulinemic clamp
Type of treatment
Injection or infusion
How many people
60 participants
Where
1 siteNetherlands
Study dates
Sep 2026to Sep 2028
Phase
Observational
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 40 years
  • All sexes
  • No healthy volunteers
  • Adult

Study population: The source population consists of adult patients with gender dysphoria, who are scheduled to start with GAHT in the Amsterdam University Medical Centre (AUMC) in Amsterdam. A total of 60 transgender individuals (30 transgender women, 30 transgender men) will be selected from this outpatient clinic.

Who may be able to join

  • Diagnosed with gender dysphoria according to DSM-V
  • Expected to start gender-affirming hormone treatment in the upcoming month

Who cannot join

  • Current or prior use of gender-affirming hormone therapy
  • Participation in other studies
  • Concomitant use of medication (specifically: antihypertensive agents, products, antidepressants, antipsychotic agents)
  • Known kidney disease (eGFR < 60 ml/min; UACR > 2.5 mg/mmol)
  • Diabetes mellitus
  • A history of cardiovascular disease (myocardial infarction; cardiac surgery or revascularization, unstable angina, heart failure, transient ischemic attack, cerebrovascular disease, or a previously undiagnosed arrhythmia)
Show all 10Show fewer
  • Known iodine-related allergies
  • Metal in the body (such as pacemaker, ICD, neurostimulator, cochlear implant, or other metal)
  • Pregnancy
  • Claustrophobia

Trial locations and contacts

1 site in 1 country. Contact the study team or a site near you to ask about taking part.

Netherlands1 site
  • Amsterdam UMC, location VU medical centre, internal medicine

    Amsterdam, North Holland

    A. S. Olde Monnikhof, Drs., +3120 444 4444, a.oldemonnikhof@amsterdamumc.nl

Other trials in Netherlands

About this study

This study investigates how sex hormones affect kidney function in people undergoing gender-affirming hormone therapy (GAHT). We know men have a faster progression of kidney disease. Earlier studies suggest that the female sex hormone estradiol may have a protective effect on kidney function while the male sex hormone testosterone may have the opposite effect. But the reasons why this happens remain unclear. By studying participants undergoing (GAHT) we gain insight into the mechanisms by which testosterone and estradiol influence the kidneys. People undergoing GAHT provide a unique chance to study how sex hormones interact with the kidneys. The results may help us to understand why men and women exhibit differences in kidney disease development. This study will include 30 men and 30 women, aged 18 to 40, who start GAHT. Participants will have three study visits, two of which will happen during their scheduled healthcare appointments. During the first visit, a screening will take place to check if patients can take part in the study. At study visits before and after one year of therapy, kidney function is measured, kidney MRI is performed, urine is collected and a small sample of fat tissue. Taking part in the study does not delay the start of GAHT.

Read the detailed description

Sex differences in kidney physiology are a vastly understudied area, despite known differences in sex-specific rates of chronic kidney disease. Kidney function decline is accelerated in men compared to women, suggesting a potential harmful role for testosterone. Transgender individuals undergoing hormone therapy provide a unique model to study the effects of gender affirming hormone therapy on kidney function and renal physiology. The central objectives of this study are to comprehensively assess the effects of gender affirming hormone therapy (GAHT; testosterone in transgender men or estradiol and an anti-androgen in transgender women) therapy on kidney function and physiology. This study is a prospective observational study. In total we will include 60 transgender individuals (30 transgender men and 30 transgender women) between 18-40 years old, scheduled to start GAHT. The primary endpoint is measured glomerular filtration rate (GFR) by iohexol clearance. Secondary endpoints include effects of GAHT on measures of intrarenal hemodynamic function including effective renal plasma flow (ERPF), proximal tubular function, insulin sensitivity and multiparametric kidney MRI (phase-contrast MRI [perfusion], arterial spin labeling [perfusion], BOLD imaging with a multi-echo spin-echo mapping R2* [oxygenation] and diffusion-weighted MRI [diffusion]). We will also isolate urinary tubuloids to further study the effect of sex hormones on kidney physiology and in these tubuloids we will assess whether the kidney protective effects are affected by sex hormones in vitro. Furthermore, endothelial cells will be harvested by J-wire, and single-cell RNA sequencing will be performed to investigate the transcriptional effects of GAHT in endothelial cells. And finally, we will look at adipose tissue gene expression.The burden for participants consists of three study visits, two of which will replace scheduled meetings that are a part of standard healthcare practice. In total, participants will receive one venipuncture and four intravenous cannulas, from which blood will be sampled (study total of 275 mL) and iohexol and p-aminohippurate will be administered to measure GFR and ERPF respectively. After measurement of kidney function, insulin sensitivity will be measured using a variable infusion of glucose and insulin (hyperinsulinemic euglycemic clamp). Patients will undergo kidney MRI which will take about 45 minutes; participants with claustrophobia are excluded. In addition, participants will be asked to collect a 24-hour urine sample on the days prior to the second and third study visit. Subcutaneous adipose tissue is collected by needle aspiration after local anesthesia. Finally, endothelial cells will be harvested. The total risk of negative effects for participants in the current study is considered low. The transgender population is a unique population in which the effects of exogenous cross-sex hormone administration can be studied. This study may provide additional data on the safety of hormone therapy in this population and may also lead to meaningful insights regarding the physiological effects of sex hormones on kidney function in humans that may help to understand observations from cohort studies which indicate differences in progression to kidney failure dependent on gender.

Being tested
P-aminohippurate clearance study, Iohexol infusion, Hyperinsulinemic clamp
Keywords
Transgender individuals, Kidney disease, Kidney injury, Gender affirming hormone treatment, Sex hormones
Medical subject headings
Kidney Diseases

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • P-aminohippurate clearance studyDiagnostic test

    To measure effective renal plasma flow (ERPF), small doses of a substance called p-aminohippurate will be used

  • Iohexol infusionDiagnostic test

    To measure glomerular filtration rate (GFR) iohexol clearance will be performed

  • Hyperinsulinemic clampDiagnostic test

    Glucose/insulin infusion to measure insulin sensitivity

Study groups in NCT07542964
Study groupRoleWhat they receive
Transgender malesIndividuals clinically scheduled to start GAHT with testosterone therapy
Receives: Diagnostic Test: P-aminohippurate clearance study; Diagnostic Test: Iohexol infusion; Diagnostic Test: Hyperinsulinemic clamp
Transgender womenIndividuals clinically scheduled to start GAHT with estradiol and anti-androgen therapy
Receives: Diagnostic Test: P-aminohippurate clearance study; Diagnostic Test: Iohexol infusion; Diagnostic Test: Hyperinsulinemic clamp

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Change in measured glomerular filtration rate (GFR)

    Measured: Baseline, 12 months after start GAHT

Secondary outcomes (8)
  1. Change in effective renal plasma flow (ERPF)

    Measured: Baseline, 12 months after start GAHT

  2. Change in systemic hemodynamic function

    Measured: Baseline, 12 months after start GAHT

  3. Change in insulin sensitivity

    Measured: Baseline, 12 months after start GAHT

  4. Change in markers of tubular physiology

    Measured: Baseline, 12 months after start GAHT

  5. Changes in multiparametric kidney MRI

    Including (phase-contrast MRI (perfusion), arterial spin labeling (perfusion), BOLD imaging with multi-echo spin-echo mapping R2* (oxygenation) and diffusion-weighted (DW) MRI (diffusion)

    Measured: Baseline, 12 months after start GAHT

  6. Changes in endothelial function

    Measured: Baseline, 12 months after start GAHT

  7. Change in adipose tissue gene expression and adipose tissue biology

    Measured: Baseline, 12 months after start GAHT

  8. Change in tubular effects of kidney protective therapies in vitro

    Measured: Baseline, 12 months after start GAHT

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted21 Apr 2026
  2. Study startSep 2026 (estimated)
  3. Primary completionSep 2028 (estimated)
  4. Study completionSep 2028 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Cohort
Time perspective
Prospective
Enrolment
60 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07542964
Sponsor's protocol ID
NL-011071
Acronym
TRANSFORM
Status last verified
Apr 2026
First submitted
10 Apr 2026
Last updated
21 Apr 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No

Questions about this trial

What is this clinical trial studying?

An observational study of Kidney Disease and Kidney Injury, run by Amsterdam UMC, location VUmc at 1 site in Netherlands.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 2 inclusion and 10 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: opening soon, as of the sponsor's last update on 21 Apr 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Netherlands. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

Each site lists its own contact: choose the nearest one under Trial locations. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Change in measured glomerular filtration rate (GFR) (time frame: Baseline, 12 months after start GAHT). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 21 Apr 2026.

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