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NCT00085722 · ClinicalTrials.gov registry record · Phase 1

Joint Injections for Osteoarthritic Knee Pain

A Phase 1 study, sponsored by University of Wisconsin, Madison.

Completed
Registry status
Phase 1
Development phase
98
Enrollment target

NCT00085722: Completed Phase 1 study, sponsored by University of Wisconsin, Madison.

NCT00085722 is a Phase 1 study that has completed, run by University of Wisconsin, Madison. The registered enrollment target is 98 participants, above the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (63% higher). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00085722, a Phase 1 study, has completed, sponsored by University of Wisconsin, Madison.

COMPLETED
Registry status
Phase 1
Development phase
98 participants
Enrollment target

Study Summary

The purpose of this study is to determine whether prolotherapy (PrT), a therapy based on injection of a sugar solution in and around the knee, can decrease pain and disability from knee osteoarthritis (OA).

Interventions

  • PROCEDURE Dextrose Prolotherapy
  • PROCEDURE Saline Prolotherapy
  • OTHER At-home physical therapy exercise group

Trial Details

FieldValue
Enrollment Target 98 participants
Start Date 2004-07
Est. Completion 2016-05-01
Phase Phase 1
University of Wisconsin, Madison

1,039 total trials

What the finished NCT00085722 record still lists

NCT00085722 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 98 participants, a relatively small participant target, above the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (63% higher).

The record links to 0 conditions, and to 3 interventions - of which Dextrose Prolotherapy is the first listed.

NCT00085722 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00085722 about?

NCT00085722 is a clinical study titled "Joint Injections for Osteoarthritic Knee Pain". The purpose of this study is to determine whether prolotherapy (PrT), a therapy based on injection of a sugar solution in and around the knee, can decrease pain and disability from knee osteoarthritis (OA).

What is the current status of trial NCT00085722?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 98 participants. The study started on 2004-07. Estimated completion is 2016-05-01.

What interventions are being tested in trial NCT00085722?

The interventions under investigation include: Dextrose Prolotherapy (PROCEDURE), Saline Prolotherapy (PROCEDURE), At-home physical therapy exercise group (OTHER).

Who is sponsoring clinical trial NCT00085722?

This trial is sponsored by University of Wisconsin, Madison, which has 1,039 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00085722's enrollment target sits among peer trials

98 592nd of 2000 higher than 1,404 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 NCT00085722, the US trial registry maintained by the National Library of Medicine. NCT00085722 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.