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NCT00297830 · ClinicalTrials.gov registry record · Phase 2

Zoledronic Acid Versus Alendronate for Prevention of Bone Loss After Organ Transplantation

A Phase 2 study, sponsored by Columbia University.

Completed
Registry status
Phase 2
Development phase
111
Enrollment target

NCT00297830: Completed Phase 2 study, sponsored by Columbia University.

NCT00297830 is a Phase 2 study that has completed, run by Columbia University. The registered enrollment target is 111 participants, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (17% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00297830, a Phase 2 study, has completed, sponsored by Columbia University.

COMPLETED
Registry status
Phase 2
Development phase
111 participants
Enrollment target

Study Summary

The purpose of this study is to compare the effectiveness and safety of zoledronic acid with alendronate in the prevention of bone loss after organ transplantation. Zoledronic acid is given as a single intravenous infusion. Alendronate is given as a weekly pill. Both are expected to be very effective, but it is not known which one will work best.

Primary Outcome

BMD was measured by dual-energy x-ray absorptiometry (QDR-4500 densitometer; Hologic, Inc., Bedford, MA); short-term in vivo coefficient of variation is 0.68% (spine) and 1.36% (femoral neck). T scores were generated using gender-specific databases provided by the manufacturer.

Interventions

  • DRUG Zoledronic acid
  • DRUG Alendronate
  • OTHER Placebo Zoledronic Acid
  • OTHER Placebo Alendronate

Trial Details

FieldValue
Enrollment Target 111 participants
Start Date 2005-11
Est. Completion 2014-01
Phase Phase 2
Columbia University

958 total trials

What the finished NCT00297830 record still lists

NCT00297830 is an interventional study that assigns participants to a tested intervention. The registered 111 participants enrollment target is mid-sized for trials with a published cap, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (17% lower).

The record links to 0 conditions, and to 4 interventions - of which Zoledronic acid is the first listed.

NCT00297830 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00297830 about?

NCT00297830 is a clinical study titled "Zoledronic Acid Versus Alendronate for Prevention of Bone Loss After Organ Transplantation". The purpose of this study is to compare the effectiveness and safety of zoledronic acid with alendronate in the prevention of bone loss after organ transplantation. Zoledronic acid is given as a single intravenous infusion. Alendronate is given as a weekly pill. Both are expected to be very effectiv...

What is the current status of trial NCT00297830?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 111 participants. The study started on 2005-11. Estimated completion is 2014-01.

What interventions are being tested in trial NCT00297830?

The interventions under investigation include: Zoledronic acid (DRUG), Alendronate (DRUG), Placebo Zoledronic Acid (OTHER), Placebo Alendronate (OTHER).

Who is sponsoring clinical trial NCT00297830?

This trial is sponsored by Columbia University, which has 958 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00297830's enrollment target sits among peer trials

111 632nd of 2000 higher than 1,369 of 2,000 other Phase 2 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 2 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 NCT00297830, the US trial registry maintained by the National Library of Medicine. NCT00297830 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.