NCT00285116

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

Trial Health

Trial Relationships

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Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

January 31, 2006

Completed
1 day until next milestone

First Posted

Study publicly available on registry

February 1, 2006

Completed
Last Updated

July 2, 2021

Status Verified

July 1, 2021

First QC Date

January 31, 2006

Last Update Submit

July 1, 2021

Conditions

Hallux RigidusFasicitis Plantaris

Outcome Measures

Primary Outcomes (1)

  • Objective evidence of hallux rigidus being a cause of fasicitis plantaris.

Interventions

Clinical examination and radiological evaluationPROCEDURE

Eligibility Criteria

Age40 Years - 65 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • Hallux rigidus or fasicitis plantaris or healthy volunteer

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Related Links

MeSH Terms

Conditions

Hallux Rigidus

Interventions

Restraint, Physical

Condition Hierarchy (Ancestors)

Foot Deformities, AcquiredFoot DeformitiesMusculoskeletal DiseasesJoint Diseases

Intervention Hierarchy (Ancestors)

Behavior ControlTherapeuticsImmobilizationInvestigative Techniques

Study Officials

  • Rene Verdonk, MD, PhD

    University Hospital, Ghent

    PRINCIPAL INVESTIGATOR
0

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NON RANDOMIZED
Masking
NONE
Purpose
DIAGNOSTIC
Intervention Model
SINGLE GROUP
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

January 31, 2006

First Posted

February 1, 2006

Last Updated

July 2, 2021

Record last verified: 2021-07