Clinical Evaluation on the Use of the X-pander Device

NCT ID: NCT01443975

Last Updated: 2014-03-31

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

COMPLETED

Total Enrollment

100 participants

Study Classification

OBSERVATIONAL

Study Start Date

2011-09-30

Study Completion Date

2013-06-30

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

The purpose of this study is to clinically evaluate the use of the x-pander device.

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

Clinical evaluation on the use of the x-pander device during THA-surgery

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Osteoarthrosis Total Hip Arthroplasty

Keywords

Explore important study keywords that can help with search, categorization, and topic discovery.

Total Hip Arthroplasty Osteoarthritis

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

All patients

Measurement with x-pander in acetabulum prior to inserting the artificial hip socket.

x-pander

Intervention Type PROCEDURE

Measurement of the size and quality of the bony acetabulum before mounting the artificial hip socket.

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

x-pander

Measurement of the size and quality of the bony acetabulum before mounting the artificial hip socket.

Intervention Type PROCEDURE

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

* Clinical diagnosis for hip osteoarthrosis

Exclusion Criteria

* Previous surgery of the actual hip
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

Company Medichanical Engineering

UNKNOWN

Sponsor Role collaborator

Northern Orthopaedic Division, Denmark

OTHER

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

Responsibility Role SPONSOR

Principal Investigators

Learn about the lead researchers overseeing the trial and their institutional affiliations.

Mogens B. Laursen, MD, PhD

Role: PRINCIPAL_INVESTIGATOR

Orthopaedic Surgery Research Unit, Aalborg Hospital, Denmark

Locations

Explore where the study is taking place and check the recruitment status at each participating site.

Ortopaedic Clinic

Farsoe Hospital, Aalborg University Hospital, , Denmark

Site Status

Ortopaedic Clinic

Frederikshavn Hospital, Aalborg University Hospital, , Denmark

Site Status

Countries

Review the countries where the study has at least one active or historical site.

Denmark

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

N-20110043

Identifier Type: -

Identifier Source: org_study_id