NCT01348178

Completed

Retrospective Follow-up Study After Periacetabular Osteotomy...

University of Aarhus Source

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Other study identifiers

Sponsor study identifier

PAO

Study Type

observational

Actual enrollment (reported)

401

Locations

0 countries

Sites

N/A

Timeline

Study Start

March 2010

Date type not reported

This date has not been verified as actual or estimated.

Primary Completion

November 2011

Actual (reported)

Study Completion

November 2011

Actual (reported)

Brief Summary

This is a retrospective study assessing pre- and postoperative radiographic indices of hip dysplasia in order to identify factors predicting failure following Periacetabular Osteotomy (PAO).

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): 401 participants
Study completion date: November 2011
Actual (reported)
Listed locations: 0 countries · 0 sites

Trial Relationships

Click on a node to explore related trials.

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
March 2010
Date type not reported
This date has not been verified as actual or estimated.
First Submitted
May 3, 2011
Actual (reported)
First Posted
May 5, 2011
Actual (reported)
Primary Completion
November 2011
Actual (reported)
Study Completion
November 2011
Actual (reported)

Last Updated: January 9, 2012
Status Verified: January 2012
Last Update Submitted: January 6, 2012

Conditions

Congenital Deformity of Hip Joints

Study Arms (1)

developmental dysplasia of the hip, PAO

All patients who underwent periacetabular osteotomy from 1999-2007 at the University Hospital of Aarhus

Procedure: Follow-up

Interventions

Follow-upProcedure

Follow-up

Also known as: Outcome, THA, WOMAC

developmental dysplasia of the hip, PAO

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

Patients who underwent PAO from 1999-2007

You may qualify if:

PAO from 1999-2007

Contact the study team to confirm eligibility.

Sponsors & Collaborators

University of Aarhus
Otherlead

MeSH Terms

Interventions

Tacrine

Intervention Hierarchy (Ancestors)

AminoacridinesAcridinesHeterocyclic Compounds, 3-RingHeterocyclic Compounds, Fused-RingHeterocyclic Compounds

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

401 participants (actual enrollment reported by the registry).

Study Design

Study Type: observational
Observational Model: COHORT
Time Perspective: RETROSPECTIVE
Sponsor Type: OTHER
Responsible Party: SPONSOR

Study Record Dates

First Submitted

May 3, 2011

First Posted

May 5, 2011

Study Start

March 2010

Date type not reported

This date has not been verified as actual or estimated.

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Primary Completion

November 2011

Actual (reported)

Study Completion

November 2011

Actual (reported)

Last Updated

January 9, 2012

Record last verified: 2012-01

Source record

Download the complete ClinicalTrials.gov record imported by Syfrah, including fields not shown in this page. The registry may contain a newer revision.

Source: ClinicalTrials.gov.

JSON downloads include source attribution and retrieval details alongside the unchanged original record or the separately normalized values.

Registry identifier: NCT01348178
Data provider: ClinicalTrials.gov
Source updated: 2012-01-09
Normalization version: ctgov-legacy-1

Open registry record

Source retrieved: 2026-10-25 22:29:24 UTC

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)

developmental dysplasia of the hip, PAO

Interventions

Eligibility Criteria

You may qualify if:

Sponsors & Collaborators

MeSH Terms

Interventions

Intervention Hierarchy (Ancestors)

Study Officials

Enrollment

Study Design

Study Record Dates

Source record