NCT01345838

Completed

Acetabular Labral Tear in Dysplastic Hips

University of Aarhus Source

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Other study identifiers

Sponsor study identifier

PAO and labrum

Study Type

observational

Actual enrollment (reported)

104

Locations

1 country

Sites

1

Timeline

Study Start

January 2010

Actual (reported)

Primary Completion

February 2013

Actual (reported)

Study Completion

September 2013

Actual (reported)

Brief Summary

A prospective case-control study of the clinical and radiographic outcome of periacetabular osteotomy in patients with and without preoperative acetabular labral tears.

Registry Overview

Registry-reported information. Elapsed time and enrollment totals alone do not measure study progress or recruitment pace.

Recruitment status: completed
Actual enrollment (reported): 104 participants
Study completion date: September 2013
Actual (reported)
Listed locations: 1 countries · 1 sites

Trial Relationships

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Some registry-reported names shown below are not yet linked in this graph.

Study Timeline

Dates and qualifiers reported by the registry. Estimated dates do not confirm that a milestone has occurred.

Study Start
January 2010
Actual (reported)
First Submitted
April 29, 2011
Actual (reported)
First Posted
May 2, 2011
Actual (reported)
Primary Completion
February 2013
Actual (reported)
Study Completion
September 2013
Actual (reported)

Last Updated: January 9, 2023
Status Verified: January 2023
Last Update Submitted: January 6, 2023

Conditions

Developmental Dysplasia of the Hip Labrum

Study Arms (1)

Dysplasia

Patients with developmental dysplasia of the hip undergoing PAO

Procedure: labrum

Interventions

labrumProcedure

Two years follow-up after PAO, to find any differences among patients with and without known acetabular labral tears

Dysplasia

Registry-reported names are shown in full. Names without a link have not yet been matched to a Syfrah profile.

Eligibility Criteria

Sexall

Healthy VolunteersNo

Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)

Sampling MethodProbability Sample

Study Population

Consecutive patients with developmental dysplasia of hip and who is scheduled for PAO

You may qualify if:

Developmental dysplasia of the hip

You may not qualify if:

Sponsors & Collaborators

University of Aarhus
Otherlead

Study Sites (1)

Orthopaedic department, Aarhus Universityhospital

Aarhus, 8000, Denmark

MeSH Terms

Conditions

Developmental Dysplasia of the Hip

Condition Hierarchy (Ancestors)

Hip DislocationJoint DislocationsJoint DiseasesMusculoskeletal DiseasesMusculoskeletal AbnormalitiesCongenital AbnormalitiesCongenital, Hereditary, and Neonatal Diseases and Abnormalities

Study Officials

Kjeld Soballe, Prof. D.Msc
Orthopedic Research Unit, Aarhus University Hospital
STUDY CHAIR
Charlotte Hartig-Andreasen, MD
Orthopedic Research Unit, Aarhus University Hospital
PRINCIPAL INVESTIGATOR

Enrollment

104 participants (actual enrollment reported by the registry).

Study Design

Study Type: observational
Observational Model: CASE CONTROL
Time Perspective: PROSPECTIVE
Sponsor Type: OTHER
Responsible Party: SPONSOR

Study Record Dates

First Submitted

April 29, 2011

First Posted

May 2, 2011

Study Start

January 2010

Actual (reported)

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Not ApplicableTerminated

NCT07111858

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Not ApplicableRecruiting

NCT00843258

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Not ApplicableCompleted

NCT01866527

Selective Ultrasound Screening for DDH 1991-2006

Completed

contraindication for magnetic resonance arthrography
severe deformities of the femural head

Contact the study team to confirm eligibility.

Primary Completion

February 2013

Actual (reported)

Study Completion

September 2013

Actual (reported)

Last Updated

January 9, 2023

Record last verified: 2023-01

Source record

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Source: ClinicalTrials.gov.

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Registry identifier: NCT01345838
Data provider: ClinicalTrials.gov
Source updated: 2023-01-09
Normalization version: ctgov-legacy-1

Open registry record

Source retrieved: 2026-10-25 22:22:00 UTC

Locations

DK(1)

Brief Summary

Registry Overview

Trial Relationships

Related Scientific Literature

Study Timeline

Study Start

First Submitted

First Posted

Primary Completion

Study Completion

Conditions

Study Arms (1)

Dysplasia

Interventions

Eligibility Criteria

You may qualify if:

You may not qualify if:

Sponsors & Collaborators

Study Sites (1)

MeSH Terms

Conditions

Condition Hierarchy (Ancestors)

Study Officials

Enrollment

Study Design

Study Record Dates

Source record

Locations