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NCT00982423 · ClinicalTrials.gov registry record · Phase 1

The Effects of Decreasing the Lasix Dose on the Cardiorenal System

A Phase 1 study, sponsored by Mayo Clinic.

Completed
Registry status
Phase 1
Development phase
41
Enrollment target

NCT00982423: Completed Phase 1 study, sponsored by Mayo Clinic.

NCT00982423 is a Phase 1 study that has completed, run by Mayo Clinic. The registered enrollment target is 41 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (32% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

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The verdict

NCT00982423, a Phase 1 study, has completed, sponsored by Mayo Clinic.

COMPLETED
Registry status
Phase 1
Development phase
41 participants
Enrollment target

Study Summary

The investigators' objective is to define the effects of decreasing the furosemide dose on heart, kidney and humoral function in people with compensated heart failure and kidney dysfunction and also in people with compensated heart failure without kidney dysfunction. Secondly, to define the humoral activation in both groups.

Primary Outcome

Kidney function was measured by GFR determined by iothalamate clearance. GFR describes the flow rate of filtered fluid through the kidney measured in milliliters per minute per 1.73 m\^2 of body surface area. A lower GFR means the kidney is not filtering normally. An estimated GFR of less than 60 mg/min/1.73 m\^2 of body surface area is considered to be impaired kidney function.

Interventions

  • DRUG Furosemide

Trial Details

FieldValue
Enrollment Target 41 participants
Start Date 2009-07
Est. Completion 2014-07
Phase Phase 1
Mayo Clinic

2,844 total trials

What the finished NCT00982423 record still lists

NCT00982423 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 41 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (32% lower).

The record links to 0 conditions, and to 1 intervention - of which Furosemide is the first listed.

NCT00982423 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00982423 about?

NCT00982423 is a clinical study titled "The Effects of Decreasing the Lasix Dose on the Cardiorenal System". The investigators' objective is to define the effects of decreasing the furosemide dose on heart, kidney and humoral function in people with compensated heart failure and kidney dysfunction and also in people with compensated heart failure without kidney dysfunction. Secondly, to define the humoral ...

What is the current status of trial NCT00982423?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 41 participants. The study started on 2009-07. Estimated completion is 2014-07.

What interventions are being tested in trial NCT00982423?

The interventions under investigation include: Furosemide (DRUG).

Who is sponsoring clinical trial NCT00982423?

This trial is sponsored by Mayo Clinic, which has 2,844 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00982423's enrollment target sits among peer trials

41 1125th of 2000 higher than 871 of 2,000 other Phase 1 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 1 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 NCT00982423, the US trial registry maintained by the National Library of Medicine. NCT00982423 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.