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NCT02003469 · ClinicalTrials.gov registry record · NA

Preventing Outcomes Through Effective Cardiovascular Risk Reduction After Transplant II

A NA study, sponsored by University of Michigan.

Completed
Registry status
NA
Development phase
67
Enrollment target

NCT02003469: Completed NA study, sponsored by University of Michigan.

NCT02003469 is a NA study that has completed, run by University of Michigan. The registered enrollment target is 67 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (95% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT02003469, a NA study, has completed, sponsored by University of Michigan.

COMPLETED
Registry status
NA
Development phase
67 participants
Enrollment target

Study Summary

Background and Rationale Cardiovascular disease is highly prevalent in the kidney transplant population, accounting for approximately 40% of all deaths and significant morbidity. The morbidity and mortality experienced by kidney transplant recipient's results from an excess of pre-transplant risk factors that are exacerbated by kidney transplantation along with the development of novel risk factors. Hypertension (HTN) is the most consistent cardiovascuar disease risk factor in transplant recipients.. A large number of studies have been done in the general population comparing ambulatory blood pressure monitoring (ABPM) to casual, office based and home measures of blood pressure (BP). The results have clearly demonstrated that ABPM gives a more accurate representation of BP and arguably should be used as part of routine patient care. ABPM has been shown to reveal patients both with white-coat and with masked HTN, nocturnal HTN and lack of nocturnal dipping. Ambulatory BP measures afford us a non-invasive, highly accurate way to evaluate and treat kidney transplant recipients. Live kidney donors (LKD) have significantly expanded the supply of critical organs. Of paramount importance of course has always been donor safety. As a result, candidates are known to be healthy at the time of donation. Ambulatory blood pressure monitoring allows a unique opportunity to examine the effects of live kidney donation on the blood pressure profiles of LKD. Methods Study Design: Prospective, 5-year, single center study of ABPM, cardiovascular and graft outcomes in incident and prevalent live kidney donors, kidney and kidney-pancreas transplant candidates and recipients.

Primary Outcome

We reassessed the ABPM pattern prior to, early after and 12 months after kidney transplant or live kidney donation to look for changes consistent with onset hypertension

Interventions

  • DEVICE Ambulatory Blood Pressure Monitoring

Trial Details

FieldValue
Enrollment Target 67 participants
Start Date 2009-04
Est. Completion 2013-09
Phase NA
University of Michigan

1,327 total trials

What the finished NCT02003469 record still lists

NCT02003469 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 67 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (95% lower).

The record links to 0 conditions, and to 1 intervention - of which Ambulatory Blood Pressure Monitoring is the first listed.

NCT02003469 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT02003469 about?

NCT02003469 is a clinical study titled "Preventing Outcomes Through Effective Cardiovascular Risk Reduction After Transplant II". Background and Rationale Cardiovascular disease is highly prevalent in the kidney transplant population, accounting for approximately 40% of all deaths and significant morbidity. The morbidity and mortality experienced by kidney transplant recipient's results from an excess of pre-transplant risk fa...

What is the current status of trial NCT02003469?

This trial is currently completed. It is a NA study. The enrollment target is 67 participants. The study started on 2009-04. Estimated completion is 2013-09.

What interventions are being tested in trial NCT02003469?

The interventions under investigation include: Ambulatory Blood Pressure Monitoring (DEVICE).

Who is sponsoring clinical trial NCT02003469?

This trial is sponsored by University of Michigan, which has 1,327 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT02003469's enrollment target sits among peer trials

67 1139th of 2000 higher than 862 of 2,000 other NA trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT02003469, the US trial registry maintained by the National Library of Medicine. NCT02003469 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.