The Correlation Between Fasicitis Plantaris and Hallux Rigidus

Sponsor
University Hospital, Ghent (Other)
Overall Status
Withdrawn
CT.gov ID
NCT00285116
Collaborator
(none)
0

Study Details

Study Description

Brief 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

Condition or Disease Intervention/Treatment Phase
  • Procedure: Clinical examination and radiological evaluation
N/A

Study Design

Study Type:
Interventional
Actual Enrollment :
0 participants
Allocation:
Non-Randomized
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Primary Purpose:
Diagnostic
Official Title:
The Correlation Between Fasicitis Plantaris and Hallux Rigidus

Outcome Measures

Primary Outcome Measures

  1. Objective evidence of hallux rigidus being a cause of fasicitis plantaris. []

Eligibility Criteria

Criteria

Ages Eligible for Study:
40 Years to 65 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Hallux rigidus or fasicitis plantaris or healthy volunteer
Exclusion Criteria:

Contacts and Locations

Locations

No locations specified.

Sponsors and Collaborators

  • University Hospital, Ghent

Investigators

  • Principal Investigator: Rene Verdonk, MD, PhD, University Hospital, Ghent

Study Documents (Full-Text)

None provided.

More Information

Additional Information:

Publications

None provided.
Responsible Party:
University Hospital, Ghent
ClinicalTrials.gov Identifier:
NCT00285116
Other Study ID Numbers:
  • 2004/204
First Posted:
Feb 1, 2006
Last Update Posted:
Jul 2, 2021
Last Verified:
Jul 1, 2021
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jul 2, 2021