The reliability of a new guidance tool voor accurate cuppositioning in total hip arthroplasty

The reliability of a new guidance tool voor accurate cuppositioning in total hip arthroplasty - Guidewire trial

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

NL-OMON

Registry ID

NL-OMON39661

Enrollment

Registered

2013-05-07

Start date

2013-04-01

Completion date

Unknown

Last updated

2024-04-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

gewrichtskraakbeen arthrosis osteoarthritis

Interventions

placement of a screw in the pelvis, and increase of operationtime of approximately 10 minutes.

Eligibility

Age

18 Years to 99 Years

Inclusion criteria

Inclusion criteria: osteoarthritis of the hip

Exclusion criteria

Exclusion criteria: obesity hip dysplasia traumatic hip injury patients with increased risk for infection

Design outcomes

Primary

Measure	Time frame
the difference of perioperative measured inclination and anteversion (by using the device) compared to the values calculated on CT.	—

Secondary

Measure	Time frame
operating time, complications, such as: infection and pain at the entrancepoint of the markingpoint.	—

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)