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NCT01911650 · ClinicalTrials.gov registry record · NA

A Pilot Study: Treatment of Achilles Tendinopathy With Platelet-Rich Plasma Therapy

A NA study, sponsored by University of Wisconsin, Madison.

Completed
Registry status
NA
Development phase
20
Enrollment target

NCT01911650 is a NA study that has completed, run by University of Wisconsin, Madison. The registered enrollment target is 20 participants.

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The verdict

NCT01911650, a NA study, has completed, sponsored by University of Wisconsin, Madison.

COMPLETED
Registry status
NA
Development phase
20 participants
Enrollment target

Study Summary

The overall goal of this proposal is to correlate ultrasound elastography technique with more standard clinically based outcome measures within the setting of a small sample sized group of patients affected by moderate-to- severe, chronic (\>6months) midsubstance Achilles tendinopathy (AT).

Interventions

  • OTHER Quality of Life Questionnaires
  • OTHER Autologous Platelet Rich Plasma
  • OTHER Ultrasound Imaging

Trial Details

FieldValue
Enrollment Target 20 participants
Start Date 2013-06
Est. Completion 2019-01-10
Phase NA

Sponsor

University of Wisconsin, Madison

1,039 total trials

What the Registry Record Tells You About NCT01911650

The ClinicalTrials.gov registry entry for NCT01911650 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 20 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is University of Wisconsin, Madison, which has 1,039 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 3 interventions - of which Quality of Life Questionnaires is the first listed.

NCT01911650 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT01911650 about?

NCT01911650 is a clinical study titled "A Pilot Study: Treatment of Achilles Tendinopathy With Platelet-Rich Plasma Therapy". The overall goal of this proposal is to correlate ultrasound elastography technique with more standard clinically based outcome measures within the setting of a small sample sized group of patients affected by moderate-to- severe, chronic (\>6months) midsubstance Achilles tendinopathy (AT).

What is the current status of trial NCT01911650?

This trial is currently completed. It is a NA study. The enrollment target is 20 participants. The study started on 2013-06. Estimated completion is 2019-01-10.

What interventions are being tested in trial NCT01911650?

The interventions under investigation include: Quality of Life Questionnaires (OTHER), Autologous Platelet Rich Plasma (OTHER), Ultrasound Imaging (OTHER).

Who is sponsoring clinical trial NCT01911650?

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

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

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.