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.
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
- Conditions the study is for
- Kidney Disease, Kidney Injury, Transgender Individuals
- 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)
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- 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
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.
- Conditions
- Kidney Disease, Kidney Injury, Transgender Individuals
- 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 group | Role | What they receive |
|---|---|---|
| Transgender males | Individuals clinically scheduled to start GAHT with testosterone therapy Receives: Diagnostic Test: P-aminohippurate clearance study; Diagnostic Test: Iohexol infusion; Diagnostic Test: Hyperinsulinemic clamp | |
| Transgender women | Individuals 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.
Change in measured glomerular filtration rate (GFR)
Measured: Baseline, 12 months after start GAHT
Secondary outcomes (8)
Change in effective renal plasma flow (ERPF)
Measured: Baseline, 12 months after start GAHT
Change in systemic hemodynamic function
Measured: Baseline, 12 months after start GAHT
Change in insulin sensitivity
Measured: Baseline, 12 months after start GAHT
Change in markers of tubular physiology
Measured: Baseline, 12 months after start GAHT
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
Changes in endothelial function
Measured: Baseline, 12 months after start GAHT
Change in adipose tissue gene expression and adipose tissue biology
Measured: Baseline, 12 months after start GAHT
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.
- First posted21 Apr 2026
- Study startSep 2026 (estimated)
- Primary completionSep 2028 (estimated)
- Study completionSep 2028 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Kidney DiseaseStudies of the same condition, open and under way.
- More trials run by Amsterdam UMC, location VUmcThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
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)
Sponsor and investigators
- Lead sponsor
- Amsterdam UMC, location VUmc
- Sponsor type
- University, hospital or other
- Collaborators
- Dutch Kidney Foundation
- Responsible party
- Principal investigator, Daniel van Raalte, Amsterdam UMC, location VUmc
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
Study at a glance
From the registry record, last updated by the sponsor on 21 Apr 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Transgender Analysis of Nephrological Studies Focused on Renal Metrics
- ClinicalTrials.gov ID
- NCT07542964
- Acronym / sponsor ID
- TRANSFORM / NL-011071
- Conditions
- Kidney Disease, Kidney Injury, Transgender Individuals
- Keywords
- Transgender individuals, Kidney disease, Kidney injury, Gender affirming hormone treatment, Sex hormones
- Study type
- Observational
- Recruitment status
- Not yet recruiting
- Enrolment
- 60 participants (estimated)
- Lead sponsor
- Amsterdam UMC, location VUmcUniversity, hospital or other
- Collaborators
- Dutch Kidney Foundation
- Study start
- Sep 2026 (estimated)
- Primary completion
- Sep 2028 (estimated)
- Study completion
- Sep 2028 (estimated)
- First posted
- 21 Apr 2026 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
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.
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.
Study design
- Observational model
- Cohort
- Time perspective
- Prospective
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| Transgender males | – | Diagnostic Test: P-aminohippurate clearance study, Diagnostic Test: Iohexol infusion, Diagnostic Test: Hyperinsulinemic clampIndividuals clinically scheduled to start GAHT with testosterone therapy |
| Transgender women | – | Diagnostic Test: P-aminohippurate clearance study, Diagnostic Test: Iohexol infusion, Diagnostic Test: Hyperinsulinemic clampIndividuals clinically scheduled to start GAHT with estradiol and anti-androgen therapy |
Who may qualify
- Ages
- 18 to 40 years
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- 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.
Key inclusion criteria (2 listed)
- Diagnosed with gender dysphoria according to DSM-V
- Expected to start gender-affirming hormone treatment in the upcoming month
Key exclusion criteria (10 listed)
- 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
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| P-aminohippurate clearance studyTo measure effective renal plasma flow (ERPF), small doses of a substance called p-aminohippurate will be used | Diagnostic test | Transgender males, Transgender women |
| Iohexol infusionTo measure glomerular filtration rate (GFR) iohexol clearance will be performed | Diagnostic test | Transgender males, Transgender women |
| Hyperinsulinemic clampGlucose/insulin infusion to measure insulin sensitivity | Diagnostic test | Transgender males, Transgender women |
Primary outcome
Change in measured glomerular filtration rate (GFR)
Time frame: Baseline, 12 months after start GAHT
8 secondary outcomes
Change in effective renal plasma flow (ERPF)
Time frame: Baseline, 12 months after start GAHT
Change in systemic hemodynamic function
Time frame: Baseline, 12 months after start GAHT
Change in insulin sensitivity
Time frame: Baseline, 12 months after start GAHT
Change in markers of tubular physiology
Time frame: Baseline, 12 months after start GAHT
Changes in multiparametric kidney MRI
Time frame: Baseline, 12 months after start GAHT
Changes in endothelial function
Time frame: Baseline, 12 months after start GAHT
Change in adipose tissue gene expression and adipose tissue biology
Time frame: Baseline, 12 months after start GAHT
Change in tubular effects of kidney protective therapies in vitro
Time frame: Baseline, 12 months after start GAHT
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 21 Apr 2026.
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part.
Amsterdam UMC, location VU medical centre, internal medicine
Amsterdam, Netherlands
1 site in 1 country: see every site and its status.
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.