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Acute Kidney InjuryRECOVER-AKINCT05014022

Non-recovery of Kidney Function After AKI

An observational study of Acute Kidney Injury, run by University of Nottingham.

Unknown status

Status not confirmed. The sponsor has not verified this record for over two years, so it may be out of date.

Official record
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Trial summary

One in five patients admitted to hospital suffer a sudden reduction in kidney function, termed acute kidney injury (AKI). Rather than kidney 'injury' being caused by physical trauma, the term describes reversible damage caused by conditions such as being dehydrated or having an infection. Read more about this study

Who is it for?
Ages 18 years and older
Conditions the study is for
Acute Kidney Injury
What is being tested?
Multiparametric renal MRI
How many people
50 participants
Where
No sites listed yet
Study dates
1 Oct 2021to 1 Apr 2022
Phase
Observational
Are there results?
None posted in the registry

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 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Study population: Hospital inpatients at Royal Derby Hospital across all areas.

Who may be able to join

  • ≥18yrs
  • Acute kidney injury stage 1-3 by KDIGO criteria
  • At least one previous serum creatinine result available for determining baseline renal function
  • Able to give informed consent

Who cannot join

  • Unable to give consent or understand written information
  • Obstructive uropathy
  • Renal transplant
  • Patient receiving palliative care
  • Patient with AKI due to recent nephrectomy
  • Patients with known or suspected acute vasculitis or glomerulonephritis requiring immunosuppression
Show all 11Show fewer
  • End-stage kidney disease (CKD stage G5 or already on RRT)
  • Serum creatinine changes that do not meet the KDIGO definition of AKI
  • MRI cohort:
  • Contraindications to MRI e.g. claustrophobia, cardiac pacemaker, metallic fragments or implants
  • Age < 50years old

About this study

Official title: Non-recovery of Kidney Function After AKI: Identifying High Risk Groups and Assessment With Multiparametric Renal MRI

One in five patients admitted to hospital suffer a sudden reduction in kidney function, termed acute kidney injury (AKI). Rather than kidney 'injury' being caused by physical trauma, the term describes reversible damage caused by conditions such as being dehydrated or having an infection. Having AKI puts patients at an increased risk of long-term health problems, especially chronic kidney disease (CKD). CKD can also lead to other important health problems including a higher risk of heart disease and stroke. If we can reduce the progression of AKI to CKD this will benefit patients.

Currently, there is a gap in the follow-up of patients after AKI due to a lack of evidence about which patients should be followed up and when. Treatments for AKI during the episode and afterwards to prevent CKD are limited. This is mainly due to a lack of understanding about how and when the kidney recovers after AKI. New tools are needed in order to better identify patients at risk of CKD after AKI. This study aims to address these gaps in our knowledge by studying a group of AKI patients in detail.

Ultimately, the aim of this study is to produce results that will allow better planning of follow-up for patients as well the planning of future research to develop new treatments to reduce the risk of CKD in people recovering from AKI.

Read the detailed description

Acute kidney injury (AKI) is a sudden loss of renal function occurring in up to 20% of hospitalised patient. People who survive an episode of AKI are at increased risk of long-term effects on their health, in particular the development or progression of chronic kidney disease (CKD). At present, there are no interventions proven to reduce the development of CKD after an episode of AKI.

A significant gap exists in the current provision of post-AKI follow-up care. Current methods of assessing renal recovery are overly reliant on serum creatinine, an imperfect measure that over-estimate the degree of renal recovery due to the effect of critical illness on muscle mass. Based on expert opinion only, it is currently recommended that everyone who has experienced AKI should have kidney function and albuminuria checked at 90 days. In reality, current practice falls significantly below these standards. Less than half of patients with the most severe AKI see a nephrologist after discharge. Even for patients who have required dialysis for AKI, follow-up rates can be as low as 12%. Lack of evidence prevents a more evolved approach. Improving post-AKI care and reducing the development or progression of CKD could therefore directly benefit large numbers of patients. This is particularly pertinent with the additional restrictions on hospital appointments due to COVID-19. More evidence is urgently needed to inform which patients need follow-up and to integrate new techniques that significantly improve assessments of renal recovery.

Important knowledge gaps make it difficult to move directly to testing new interventions in randomised trials. AKI is not a single condition, rather a heterogeneous syndrome with a variety of causes affecting a wide range of people. Outcomes differ between clinical settings and are affected by factors related to AKI (e.g. its severity or duration), but also by an individual's co-existing long-term conditions, and possibly by their frailty. As well as CKD development, AKI is associated with higher long-term mortality rates, increased heart failure events, hospital readmissions, recurrent AKI and poorer quality of life. Which groups are most at risk of the different outcomes is not well established; similarly the groups that would have the greatest benefit from interventions to reduce the development of CKD are not currently known. It is therefore likely that subgroups of people who have sustained AKI will benefit from different models of post- AKI care i.e. a one-size fits all approach is unlikely to be beneficial or cost-effective. Finally, the timing of the renal recovery phase after an episode of AKI is poorly understood outside of experimental models, which differ in a number of ways from clinical AKI. Failure of recovery of creatinine by 90 days after AKI strongly associates with subsequent long-term reductions in renal function, suggesting that interventions may be needed prior to this time point, but descriptions of renal recovery between AKI and 90 days are lacking.

MRI has emerged as an imaging modality with promise to improve the understanding and characterisation of renal pathophysiology. It is a versatile technique in which structural and functional MRI measurements can be performed in a single multiparametric scan session to assess altered renal tissue microstructure, oxygenation, perfusion and blood flow. MRI is non-invasive, safe and avoids sampling bias by characterising the entire kidney with high spatial resolution. MRI does not involve ionising radiation, is repeatable (allowing serial assessments over time) and the MRI measures do not require gadolinium contrast agents. A series of recent systematic reviews covering the main functional renal MRI measures conclude that evidence is now needed to accelerate the translation of multiparametric renal MRI for clinical use. The reviews focussed on: arterial spin labelling (ASL, a measure of renal perfusion); Blood Oxygen Level Dependent (BOLD, sensitive to changes in renal oxygenation); longitudinal (T1) relaxation time (increases with scarring, correlates with fibrosis in the heart and liver; diffusion weighted imaging (DWI, sensitive to changes in renal tissue microstructure); and Phase Contrast (PC-MRI, a measure of renal artery blood flow).

Considering the high incidence of AKI, the long-term consequences of AKI present a major unmet clinical need affecting large numbers of people, with no proven interventions nor data to inform optimal care provision. If patients at risk of developing CKD could be better identified, this would provide a basis upon which interventions to improve patient outcomes could be planned.

The outputs of this study would directly inform planning of future research in the following ways:

  • Collection of data supporting a larger prospective cohort study of AKI patients, using data from this study to directly inform study design and MRI protocols
  • Identification of those at greatest risk of developing CKD after AKI will make clinical trials more efficient and more likely to succeed
  • Increasing understanding of the time course of renal recovery will allow planning of the optimal time points for interventions and patient follow-up
  • Demonstrate the potential application of renal MRI in NHS scanners leading to improved clinical evaluation of patients
Being tested
Multiparametric renal MRI
Medical subject headings
Acute Kidney Injury

What participants receive

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

  • Multiparametric renal MRIDiagnostic test

    10 patients in the cohort will undergo MRI scanning at day 30 and 90

What is being measured

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

  1. Number of patients who have non-recovery of renal function after an episode of AKI

    Defined as improvement of creatinine to less than 50% above baseline i.e. reversal of AKI diagnostic criteria

    Measured: 30, 60 and 90 days

Secondary outcomes (9)
  1. 90 day mortality

    Day 90 data - based on status (alive/dead) at day 90

    Measured: 90 days

  2. Hospital readmission rates

    Number of times patients has been admitted to hospital based on hospital records

    Measured: 90 days

  3. Quality of life score

    Based on EQ5D (euroqol.org) scoring system. Descriptive scoring, lower number = higher quality of life

    Measured: 90 days

  4. Fatigue score

    Based on Brief Fatigue Inventory scoring (lower score = less fatigue)

    Measured: 90 days

  5. Number of patients who have ongoing albuminuria over time

    Progression / recovery over time. Urine albumin:creatinine ratio

    Measured: Day 30,60 and 90

  6. Descriptive analysis of preferred follow-up models

    Based on structured questioning of participants

    Measured: 90 days

  7. Change in renal structure over time

    As measured by T1, total kidney volume \& DWI

    Measured: Day 30 & 90

  8. Change in renal haemodynamics over time

    As measured by ASL and phase-contrast MRI

    Measured: Day 30 & 90

  9. Change in renal oxygenation over time

    As measured by TRUST MRI

    Measured: Day 30 & 90

Timeline

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

  1. First posted20 Aug 2021
  2. Study start1 Oct 2021 (estimated)
  3. Primary completion1 Apr 2022 (estimated)
  4. Study completion1 Apr 2022 (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
50 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT05014022
Sponsor's protocol ID
21057
Other IDs
302569
Acronym
RECOVER-AKI
Status last verified
Aug 2021
First submitted
4 Aug 2021
Last updated
20 Aug 2021
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 Acute Kidney Injury, run by University of Nottingham.

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 4 inclusion and 11 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: status not confirmed, as of the sponsor's last update on 20 Aug 2021. Status can change between updates, so confirm with the study contact before making plans.

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?

Results are not available in the source record.

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

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Number of patients who have non-recovery of renal function after an episode of AKI (time frame: 30, 60 and 90 days). 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 20 Aug 2021.

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