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NCT03213015

Correlation Between the Amplitude of Ankle Dorsiflexion and Occurrence of Patellofemoral Pain Syndrome

Completed NA Last updated 13 July 2017
What this trial tests

NA trial testing Ankle dorsiflexion measurement in Patellofemoral Pain Syndrome in 67 participants. Completed in 30 June 2017.

Timeline
25 January 2017
Primary endpoint
25 March 2017
30 June 2017

Quick facts

Lead sponsorFilipe Abdalla dos Reis
PhaseNA
StatusCompleted
Study typeINTERVENTIONAL
Designsequential
Maskingnone
Primary purposediagnostic
Enrollment67
Start date25 January 2017
Primary completion25 March 2017
Estimated completion30 June 2017
Sites1 location across Brazil

Drugs / interventions tested

Conditions studied

Sponsor

Filipe Abdalla dos Reis

Who can join

Adults 18 to 55, female only, with Patellofemoral Pain Syndrome. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The aim of this study was to verify the clinical reliability of ankle dorsiflexion range of motion (ADROM) measurement with weight bearing (WB) using an app on the smartphone (iHand) and to verify if there is correlation between the limitation of the ADROM and the PFP.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

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Other recruiting trials for Patellofemoral Pain Syndrome

Currently open trials in the same condition.

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Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT03213015.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing