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NCT00285116 Clinical Trial

The Correlation Between Fasicitis Plantaris and Hallux Rigidus

Hallux Rigidus Clinical Trial

Official title:
The Correlation Between Fasicitis Plantaris and Hallux Rigidus

Clinical Trial Details — Status: Withdrawn

Administrative data
NCT number NCT00285116
Other study ID # 2004/204
Secondary ID
Status Withdrawn
Phase N/A
First received
Last updated

Study information
Verified date July 2021
Source University Hospital, Ghent
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Comparison between 3 groups: - group I has hallux rigidus. Is fasicitis plantaris present? - group II has fasicitis plantaris. Does the hallux have limited mobility? - group III does not have hallux rigidus or fasicitis plantaris

Recruitment information / eligibility
Status Withdrawn
Enrollment 0
Est. completion date
Est. primary completion date
Accepts healthy volunteers No
Gender All
Age group 40 Years to 65 Years
Eligibility Inclusion Criteria: - Hallux rigidus or fasicitis plantaris or healthy volunteer Exclusion Criteria: -

Study Design

Related Conditions & MeSH terms

Intervention

Procedure:
• Clinical examination and radiological evaluation

Locations
Country Name City State
n/a

Sponsors (1)
Lead Sponsor Collaborator
University Hospital, Ghent

Outcome
Type Measure Description Time frame Safety issue
Primary Objective evidence of hallux rigidus being a cause of fasicitis plantaris.
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