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RecruitingNCT06572215DYNAMOUpdated Apr 1, 2026

DYNAMic Renal Assessment: NOvel Methods to Assess KIDNEY Functional Reserve

An observational study in Chronic Kidney Diseases, sponsored by King's College Hospital NHS Trust. Recruiting at 1 site in United Kingdom. Open to participants aged 40 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-04-01.

Sponsored by King's College Hospital NHS Trust · Observational

From the registry’s dates

  • Started Dec 2023; still recruiting 2 years 9 months later.
Study type
Observational
Model
Case-control
Time perspective
Cross-sectional
Enrollment
44
Ages
40 Years and older
Sex
All
01

Study summary

This is a feasibility study to assess new, more practical ways of measuring renal reserve.

Read the detailed description

Quantification of glomerular filtration rate (GFR) over time is the standard assessment of kidney function. In clinical practice, the endogenous marker, 'serum creatinine' concentration, is used as a static assessment of kidney function to estimate GFR. However, serum creatinine fails to increase until at least 50% of kidney tissue is lost,[2] thus is an inadequate indicator of early CKD.

GFR like many other physiological processes is not static and augments temporarily to stimuli such as exercise and protein intake, by up to 25% from baseline in healthy individuals.[3] Similar to cardiac function stress tests which predict adverse outcomes, inability to respond to renal stressors or 'reduced renal reserve' has been demonstrated to occur prior to development of CKD (e.g. in patients with diabetes and previous acute kidney injury (AKI)) and is associated with vulnerability to future AKI, despite the presence of apparently normal kidney function measured by serum creatinine concentration.[4] Renal reserve is lost with progressive CKD,[4] and has also been demonstrated to relate to severity of histological lesions.[5]

Current measurements of renal reserve (stimulated increase in GFR due to augmented renal blood flow above basal fasting values) involve administration of a compound that is freely filtered by the glomerulus, unaffected by tubular function and is physiologically inert, with assessment before and after an oral protein load or amino acid infusion which induces arterial vasodilation, increasing renal blood flow and GFR

The study proposes a comparison of two novel methods of 'dynamic renal function testing' with renal reserve testing.

02

Conditions studied

  • Chronic Kidney Diseases
03

In context

Renal Insufficiency, Chronic

3,144 studies on the registry are indexed under Renal Insufficiency, Chronic; 704 are open to participants now.

This study's planned enrollment of 44 is below the median of 200 across 867 observational studies indexed under Renal Insufficiency, Chronic.

Browse Renal Insufficiency, Chronic studies →

Lead sponsor

King's College Hospital NHS Trust is the lead sponsor of 164 studies on the registry; 54 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
40 Years and older
Sexes eligible
All
Accepts healthy volunteers
Yes
Sampling method
Probability sample

Study population

: 44 Participants

Inclusion criteria

  • Patients with sickle cell nephropathy, diagnosed clinically or histologically. Sickle Cell patients will be confirmed Hb SS and eGFR (CKD-EPI) ≥ 135 ml/min/1.73m2 OR
  • Previous living kidney donation
  • Age ≥ 4No contraindication or known allergy to any trial medications.
  • Willing and able to provide written informed consent

Exclusion criteria

Exclusion:

  • Aged \< 40
  • Unable or unwilling to provide informed consent
  • Breastfeeding or pregnant women
  • Patients involved in other interventional research studies.
05

Study design

Observational model
Case-control
Time perspective
Cross-sectional
Enrollment
44 participants (estimated)
Patient registry
No
Biospecimen retention
Samples without dna

Groups and cohorts

  • Healthy Participants

    Drug: Dapagliflozin

  • Patients with hyperfiltration

    Drug: Dapagliflozin

Interventions

  • DrugDapagliflozin

    On Day 3 to 16, participants will take 10mg dapaglifozin (SGLT-2 inhibitor) orally once daily.

06

What researchers measure

Primary outcomes

  1. Change in eGFR from baseline to 2hours after oral protein load

    Time frame: 2 hours

07

Study locations

1 of 1 sites recruiting
  • King's College Hospital
    London, United Kingdom
    Recruiting
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Apr 1, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT06572215
Lead sponsor
King's College Hospital NHS Trust
Collaborators
King's College London
Responsible party
Sponsor
First posted
Aug 27, 2024
Start date
Dec 14, 2023
Primary completion
Dec 31, 2027 (estimated)
Completion
Dec 31, 2027 (estimated)
Last update
Apr 1, 2026

Study contacts

Kate Bramham, Doctor
Contact
kch-tr.research@nhs.net
0203 299 9000

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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