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NCT01588730 · ClinicalTrials.gov registry record · Phase 4
Dynamic and Static Splinting as a Treatment for Plantar Faciiopathy
A Phase 4 study, sponsored by Dynasplint Systems.
- Terminated
- Registry status
- Phase 4
- Development phase
- 26
- Enrollment target
NCT01588730 is a Phase 4 study that was terminated before completion, run by Dynasplint Systems. The registered enrollment target is 26 participants.
The verdict
NCT01588730, a Phase 4 study, was terminated before completion, sponsored by Dynasplint Systems.
- TERMINATED
- Registry status
- Phase 4
- Development phase
- 26 participants
- Enrollment target
Study Summary
The purpose of this study is to compare the Ankle Dorsiflexion Dynasplint System (DS) to static night splint for the reduction of pain from Plantar Fasciitis (Fasciopathy).
Interventions
- DEVICE Ankle Dorsiflexion Dynasplint
- PROCEDURE Commercially Available Static Night splint
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 26 participants |
| Start Date | 2011-06 |
| Phase | Phase 4 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT01588730
The ClinicalTrials.gov registry entry for NCT01588730 describes a study currently listed as terminated, categorized as Phase 4. The registered enrollment target is 26 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Dynasplint Systems, which has 9 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 2 interventions - of which Ankle Dorsiflexion Dynasplint is the first listed.
NCT01588730 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT01588730 about?
NCT01588730 is a clinical study titled "Dynamic and Static Splinting as a Treatment for Plantar Faciiopathy". The purpose of this study is to compare the Ankle Dorsiflexion Dynasplint System (DS) to static night splint for the reduction of pain from Plantar Fasciitis (Fasciopathy).
What is the current status of trial NCT01588730?
This trial is currently terminated. It is a Phase 4 study. The enrollment target is 26 participants. The study started on 2011-06.
What interventions are being tested in trial NCT01588730?
The interventions under investigation include: Ankle Dorsiflexion Dynasplint (DEVICE), Commercially Available Static Night splint (PROCEDURE).
Who is sponsoring clinical trial NCT01588730?
This trial is sponsored by Dynasplint Systems, which has 9 total clinical trials registered on ClinicalTrials.gov.
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