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NCT00048438 · ClinicalTrials.gov registry record · Phase 3

Safety and Efficacy of Zemplar Capsule in Reducing Serum IPTH Levels in Chronic Kidney Disease Subjects (Three Times Weekly)

A Phase 3 study of Renal Insufficiency, Chronic, sponsored by Abbott.

Completed
Registry status
Phase 3
Development phase
68
Enrollment target
18
Study locations

NCT00048438 is a Phase 3 study of Renal Insufficiency, Chronic that has completed, run by Abbott. The registered enrollment target is 68 participants, below the 645-participant average among 14 other Renal Insufficiency, Chronic trials with a reported enrollment target (89% lower). The trial reports 18 study locations across 13 states.

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The verdict

NCT00048438, a Phase 3 study of Renal Insufficiency, Chronic, has completed, sponsored by Abbott.

COMPLETED
Registry status
Phase 3
Development phase
68 participants
Enrollment target
18
Study locations

Study Summary

The objective of this study is to determine whether paricalcitol is safe and effective compared to placebo in reducing elevated serum PTH levels in patients with chronic kidney disease.

Interventions

  • DRUG paricalcitol

Study Locations (18)

Florida

  • Outcomes Research International, Inc. - Hudson
  • Nephrology Association of South Miami - Miami
  • Tampa Bay Nephrology Associates - Tampa

Missouri

  • University of Missouri Health Sciences Center - Columbia
  • Arms, Dodge, Robinson, Wilber and Crouch - Kansas City
  • Washington University School of Medicine - St Louis

New York

  • North Shore University Hospital - Great Neck
  • Mount Sinai School of Medicine - New York

California

  • UCI Medical Center - Orange

Colorado

  • Western Nephrology - Thornton

Illinois

  • Northwestern University Medical School - Chicago

Nevada

  • NEA Research - Las Vegas

North Carolina

  • Wake Nephrology Associates, PA - Raleigh

Trial Details

FieldValue
Enrollment Target 68 participants
Start Date 2002-02
Phase Phase 3

Sponsor

Abbott

181 total trials

What the Registry Record Tells You About NCT00048438

The ClinicalTrials.gov registry entry for NCT00048438 describes a study currently listed as completed, categorized as Phase 3. The registered enrollment target is 68 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 645-participant average among 14 other Renal Insufficiency, Chronic trials with a reported enrollment target (89% lower). The listed sponsor is Abbott, which has 181 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Renal Insufficiency, Chronic appearing as the primary indexed condition, and to 1 intervention - of which paricalcitol is the first listed.

NCT00048438 reports 18 study locations spanning 13 distinct geographic areas - top geographies include Florida, Missouri, New York.

Frequently Asked Questions

What is clinical trial NCT00048438 about?

NCT00048438 is a clinical study titled "Safety and Efficacy of Zemplar Capsule in Reducing Serum IPTH Levels in Chronic Kidney Disease Subjects (Three Times Weekly)". The objective of this study is to determine whether paricalcitol is safe and effective compared to placebo in reducing elevated serum PTH levels in patients with chronic kidney disease.

What is the current status of trial NCT00048438?

This trial is currently completed. It is a Phase 3 study. The enrollment target is 68 participants. The study started on 2002-02.

What conditions does trial NCT00048438 study?

This clinical trial studies the following conditions: Renal Insufficiency, Chronic.

What interventions are being tested in trial NCT00048438?

The interventions under investigation include: paricalcitol (DRUG).

Who is sponsoring clinical trial NCT00048438?

This trial is sponsored by Abbott, which has 181 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT00048438 being conducted?

This trial has 18 study locations across California, Colorado, Florida, Illinois, Missouri. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.