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Renal Replacement TherapyHA-AKINCT01151514

Referral Patterns for Hospital Acquired Acute Kidney Injury and Relevance to Renal Outcomes

An observational study of Renal Replacement Therapy and Mortality, run by Centre Hospitalier Universitaire Vaudois at 1 site in Switzerland.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

Few studies analyzed the referral time to nephrologists and its impact on the patient outcome in a large cohort. The investigators described the incidence and determined the outcome with respect to renal function recovery, renal replacement therapy (RRT) requirement and in-hospital mortality of Hospital Acquired Acute… Read more about this study

Who is it for?
Ages 18 to 90 years
Conditions the study is for
Renal Replacement Therapy, Mortality
What is being tested?
Nephrologist referral
How many people
Not given
Where
1 siteSwitzerland
Study dates
Start not givento not given
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 to 90 years
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Study population: This study population consisted of patients who were hospitalized in the medical and surgical departments as well as in the intensive care untis (ICU) of the University Hospital of Lausanne (Centre Hospitalier Universitaire Vaudois [CHUV]) that is a tertiary care academic medical center. Patients with AKI coming from ICU in the medicine or surgery wards, and patients from medicine or surgery wards, who required a transfer to ICU during the hospital stay, were also included whatever the cause of the transfer.

Who may be able to join

  • Adult patients.
  • Hospitalization in the medicine and surgery wards and in the intensive care unit.
  • Hospitalized patients with acquired acute kidney injury according to the
  • Acute Kidney Injury Network (AKIN)criteria.
  • HA-AKI patients with no referral to the nephrologist (nrHA-AKI).
  • HA-AKI patients referred late (more than five days [> 5 days]) to the nephrologist (lrHA-AKI).
  • HA-AKI patients early referred (within five days after sCr increase) to the nephrologist (erHA-AKI).

Who cannot join

  • Patients with AKI at the time of the hospital admission and during the first
  • 48 hours after admission.
  • Patients hospitalized in other wards.
  • Children under 18.

Trial locations and contacts

1 site in 1 country.

Switzerland1 site
  • Nephrology - CHCVs

    Sion, 1951

Other trials in Switzerland

About this study

Few studies analyzed the referral time to nephrologists and its impact on the patient outcome in a large cohort. The investigators described the incidence and determined the outcome with respect to renal function recovery, renal replacement therapy (RRT) requirement and in-hospital mortality of Hospital Acquired Acute Kidney Injury (HA-AKI) without nephrology referral (nrHA-AKI) and late referred HA-AKI patients to nephrologists (lrHA-AKI) compared with early referral patients (erHA-AKI). The patients included were admitted to the tertiary care academic center of Lausanne (Switzerland) between 2004 and 2008, in the medical and surgical services and in the intensive care unit (ICU).

Being tested
Nephrologist referral
Keywords
No referral, Late referral, Acute kidney injury, Intensive care unit, In-hospital mortality, Renal outcome, Requirement for renal replacement therapy, Length of hospital stay, Impact, Incidence
Medical subject headings
Acute Kidney Injury, Tooth, Impacted

What participants receive

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

  • Nephrologist referralOther

    Also called Control group: early-referred patients with HA-AKI.

    Nephrologist specialty, renal replacement therapy

Study groups in NCT01151514
Study groupRoleWhat they receive
nrHA-AKI patientsPatients with hospital-acquired acute kidney injury not referred to the nephrologists
Receives: Other: Nephrologist referral
lrHA-AKI patientsPatients with hospital-acquired acute kidney injury whao are late referred to the nephrologists
Receives: Other: Nephrologist referral

What is being measured

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

  1. Referral patterns for hospital acquired acute kidney injury and relevance to renal outcomes

    Recovery of renal function during hospital stay. Requirement for renal replacement therapy.

Secondary outcomes (1)
  1. Referral patterns for hospital acquired acute kidney injury and relevance to renal outcomes

    Length of hospital stay. In-hospital mortality.

Timeline

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

  1. First posted28 Jun 2010 (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
Retrospective
IDs, dates and publications
ClinicalTrials.gov ID
NCT01151514
Sponsor's protocol ID
HA-AKI referral
Acronym
HA-AKI
Status last verified
Aug 2010
First submitted
23 Jun 2010
Last updated
28 Jun 2010
Results posted
No
Data monitoring committee
Yes

Questions about this trial

What is this clinical trial studying?

An observational study of Renal Replacement Therapy and Mortality, run by Centre Hospitalier Universitaire Vaudois at 1 site in Switzerland.

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 7 inclusion and 4 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: finished, as of the sponsor's last update on 28 Jun 2010. 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 Switzerland. 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?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

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?

Referral patterns for hospital acquired acute kidney injury and relevance to renal outcomes. 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 28 Jun 2010.

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