NCT00284310

Brief Summary

The purpose of this trial is to follow-up on patients who underwent different types of wrist surgery: 4-row arthrodesis or proximal row carpectomy.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
30

participants targeted

Target at below P25 for not_applicable

Timeline
Completed

Started Oct 2005

Typical duration for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

October 1, 2005

Completed
4 months until next milestone

First Submitted

Initial submission to the registry

January 30, 2006

Completed
1 day until next milestone

First Posted

Study publicly available on registry

January 31, 2006

Completed
2.4 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

July 1, 2008

Completed
5 months until next milestone

Study Completion

Last participant's last visit for all outcomes

December 1, 2008

Completed
Last Updated

December 20, 2022

Status Verified

December 1, 2014

Enrollment Period

2.8 years

First QC Date

January 30, 2006

Last Update Submit

December 15, 2022

Conditions

Wrist Surgery

Keywords

Wrist surgery: 4-corner arthrodesis or proximal row carpectomy

Outcome Measures

Primary Outcomes (1)

  • Results of both types of wrist surgery

    5 to 10 years follow up

Study Arms (1)

wrist surgery

EXPERIMENTAL
Procedure: Anamnesis and clinical examination

Interventions

Anamnesis and clinical examinationPROCEDURE

Anamnesis and clinical examination to follow.

wrist surgery

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • All patients who underwent wrist surgery (4-row arthrodesis or proximal row carpectomy) between 1998 and 2004

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

University Hospital Ghent

Ghent, 9000, Belgium

Location

Related Links

MeSH Terms

Interventions

Immunologic MemoryRestraint, Physical

Intervention Hierarchy (Ancestors)

Adaptive ImmunityImmunityImmune System PhenomenaBehavior ControlTherapeuticsImmobilizationInvestigative Techniques

Study Officials

  • Rene Verdonk, MD, PhD

    University Hospital, Ghent

    PRINCIPAL INVESTIGATOR

Study Design

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

Study Record Dates

First Submitted

January 30, 2006

First Posted

January 31, 2006

Study Start

October 1, 2005

Primary Completion

July 1, 2008

Study Completion

December 1, 2008

Last Updated

December 20, 2022

Record last verified: 2014-12

Locations

BE(1)