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NCT01134315 · ClinicalTrials.gov registry record

Study to Evaluate Safety of Vitamin D Receptor Activators in Patients Ages 0 to 16 With Chronic Kidney Disease Stage 5 Receiving Peritoneal Dialysis Within Current Clinical Practice

A clinical trial, sponsored by AbbVie (prior sponsor, Abbott).

Terminated
Registry status
61
Enrollment target

NCT01134315 is a clinical trial that was terminated before completion, run by AbbVie (prior sponsor, Abbott). The registered enrollment target is 61 participants.

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The verdict

NCT01134315 was terminated before completion, sponsored by AbbVie (prior sponsor, Abbott).

TERMINATED
Registry status
61 participants
Enrollment target

Study Summary

The objective of this study was to observe the safety of paricalcitol utilization in pediatric participants (ages 0 to 16 years old) being treated for secondary hyperparathyroidism (SHPT). Participants were to be followed for a minimum of 3 months and up to approximately 36 months to monitor the incidence of hypercalcemia (high calcium levels in blood).

Interventions

  • DRUG Paricalcitol
  • DRUG Calcitriol

Trial Details

FieldValue
Enrollment Target 61 participants
Start Date 2010-06
Est. Completion 2012-05

Sponsor

AbbVie (prior sponsor, Abbott)

88 total trials

What the Registry Record Tells You About NCT01134315

The ClinicalTrials.gov registry entry for NCT01134315 describes a study currently listed as terminated, categorized as an unspecified phase. The registered enrollment target is 61 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is AbbVie (prior sponsor, Abbott), which has 88 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 2 interventions - of which Paricalcitol is the first listed.

NCT01134315 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT01134315 about?

NCT01134315 is a clinical study titled "Study to Evaluate Safety of Vitamin D Receptor Activators in Patients Ages 0 to 16 With Chronic Kidney Disease Stage 5 Receiving Peritoneal Dialysis Within Current Clinical Practice". The objective of this study was to observe the safety of paricalcitol utilization in pediatric participants (ages 0 to 16 years old) being treated for secondary hyperparathyroidism (SHPT). Participants were to be followed for a minimum of 3 months and up to approximately 36 months to monitor the inc...

What is the current status of trial NCT01134315?

This trial is currently terminated. The enrollment target is 61 participants. The study started on 2010-06. Estimated completion is 2012-05.

What interventions are being tested in trial NCT01134315?

The interventions under investigation include: Paricalcitol (DRUG), Calcitriol (DRUG).

Who is sponsoring clinical trial NCT01134315?

This trial is sponsored by AbbVie (prior sponsor, Abbott), which has 88 total clinical trials registered on ClinicalTrials.gov.

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.