Study of Patients With Acute Renal Failure on CVVH

NCT ID: NCT00207909

Last Updated: 2016-06-14

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

39 participants

Study Classification

OBSERVATIONAL

Study Start Date

2005-02-28

Study Completion Date

2010-03-31

Brief Summary

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Acute kidney failure is common in children in the Pediatric Intensive Care Unit (PICU). You are being asked to participate in this study because your child is being treated for kidney failure with continuous veno-venous hemofiltration (CVVH). CVVH is a continuous, gentle form of removing excess fluids and small wastes from the blood, similar to kidney dialysis (artificial kidney). It is an accepted therapy for temporary support of kidney failure. In some patients with acute kidney failure, beginning CVVH is followed by a temporary decrease of urine output. The reason why this happens is currently unknown. The purpose of this study is to determine why this happens.

Detailed Description

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Acute renal failure is common in children in the pediatric intensive care unit. Renal replacement therapies such as peritoneal dialysis (PD), intermittent hemodialysis (IHD), and continuous venovenous hemofiltration (CVVH) have been used in the management of acute renal failure. CVVH is becoming increasingly utilized in pediatric acute renal failure. However, in patients who have acute renal failure, the institution of CVVH is often followed by a progression to oliguria or anuria. The underlying pathophysiology of this change is unknown. We believe that this progression is influenced by changes in the renin-angiotensin axis, cytokine response, and other modifiers of renal hemodynamics. By serially measuring components of those systems, this study will attempt to elucidate the pathophysiology of the decreased urine output seen with institution of CVVH. Once this process is understood, future studies should focus on prevention and treatment of this complication.

General Hypothesis

The decrease in urine output seen after the initiation of CVVH is associated with increased angiotensin converting enzyme (ACE) levels, increased renin activity, increased angiotensin II levels, increased atrial naturetic peptide (ANP) levels, increased endothelin-1 levels, increased arginine vasopressin (AVP) levels, and alterations of cytokine levels and modulators of apoptosis.

Conditions

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Renal Failure

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Eligibility Criteria

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Inclusion Criteria

The general goal of patient selection is to enroll all children for whom CVVH is instituted.


Age

* 6 months -18 years old
* Patients less than 6 months of age on ECMO (addendum #1)

Indication for CVVH: including, but not limited to :

* Acute Renal Failure
* Oliguria
* Anuria
* Hyperkalemia
* Severe acidemia
* Azotemia
* Pulmonary Edema
* Uremic complications
* Severe electrolyte abnormalities
* Drug overdose with a filterable toxin
* Anasarca
* Rhabdomyolysis

Exclusion Criteria

* Age

* Less than 6 months old (unless on ECMO)
* Greater than 18 years old Weight
* Less than 5 kilograms (unless ON ECMO) Location
* Cardiac Intensive Care Unit
* Neonatal Intensive Care Unit

Non-adherence:

Inability or unwillingness of the legal guardian to provide consent or inability or unwillingness of the child to provide assent
Minimum Eligible Age

5 Months

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Children's Healthcare of Atlanta

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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James D Fortenberry, MD

Role: PRINCIPAL_INVESTIGATOR

Children's Healthcare of Atlanta

Locations

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Children's Healthcare of Atlanta at Egleston

Atlanta, Georgia, United States

Site Status

Countries

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United States

Other Identifiers

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06585

Identifier Type: -

Identifier Source: secondary_id

04-114

Identifier Type: -

Identifier Source: org_study_id

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