Skip to content

True Incidence of Hip Dislocation After Primary THA - a Nationwide Population Study

True Incidence of Hip Dislocation After Primary THA - a Nationwide Population Study

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03859791
Enrollment
32500
Registered
2019-03-01
Start date
2018-01-01
Completion date
2019-10-01
Last updated
2019-03-01

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

Conditions

Hip Dislocation

Brief summary

The primary objective is to report the true incidence of hip dislocations in primary THA patients within 2 years of index surgery. Secondary, patient and component characteristics (age, sex, comorbidity, cemented/uncemented, approach, head diameter) are analyzed as potential risk factors for dislocation. Specific components may be analyzed based on number.

Detailed description

Based on published literature and personal experience, most hip surgeons have an assumption of the degree of hip dislocation. This will be the first study to reveal the actual extent of this specific complication in a large population. It will give surgeons knowledge of the current standards -both on a national and hospital level. Depending on the results and comparisons to relevant countries, the investigators will be able to either substantiate or forced to rethink current procedures. This applies to both surgical access and use of specific components. Since the vast majority of dislocations appear within 1-2 years after primary surgery (29), the follow-up period will be 2 years. By applying the National Patient Registry the investigators are able to identify any type of patient contact with the hospital system throughout Denmark in these 2 years. Patients assigned with correct diagnostic and procedural codes for dislocation and reduction are identified. However, the investigators will also find the cases of dislocation that are incorrectly coded in the registry. Therefore, the investigators will manually look in all the patient files from orthopedic contacts regardless of assigned diagnostic and procedural codes. Additionally, emergency room and internal medicine contacts are scanned with a broad and comprehensive range of relevant hip- and dislocation-related codes to identify episodes of hip dislocation, which are incorrectly coded. These patient files will also be manually reviewed. If a patient is revised within the first 2 years, the follow-up period ends on the revision date. Revisions are also registered in the Danish Hip Arthroplasty Registry. However, the completeness is 93-95% and therefore lower than for primary operations. In order to have the complete set of revisions, the investigators will enrich our data with an extraction from the National Patient Registry by applying all approved hip revision codes

Interventions

OTHERTHA

Study participants have received a total hip arthroplasty due to arthritis. We do not make further intervention.

Sponsors

University of Southern Denmark
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
40 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* patients with the diagnosis primary/idiopathic hip OA and inserted THA from 01.01.2010 - 31.12.2014.

Exclusion criteria

* patients receiving a resurfacing hip arthroplasty and hip revisions * patients with incomplete registry data * patients with previous hip surgery

Design outcomes

Primary

MeasureTime frameDescription
Hip dislocation2 years.The true incidence of hip dislocation calculated as proportion presented with 95% confidence intervals (CI).

Secondary

MeasureTime frameDescription
Sex2 years.Potential risk factor found by logistic regression analysis
Comorbidity2 years.Potential risk factor found by logistic regression analysis
Fixation of components2 years.Potential risk factor found by logistic regression analysis
Age2 years.Potential risk factor found by logistic regression analysis
Head diameter of prosthesis2 years.Potential risk factor found by logistic regression analysis
Time to dislocation2 years.Time to first dislocation presented by Kaplan-Meier plot.
Development in complication (dislocation) over time.5 years.Incidence each year (2010-2014) calculated as proportion presented with 95% confidence intervals (CI) and compared statistically depending on distribution.
Surgical approach2 years.Potential risk factor found by logistic regression analysis

Countries

Denmark

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026