Health-related Quality of Life in Patients Undergoing Surgery for Pectus Carinatum

NCT ID: NCT01692392

Last Updated: 2014-08-05

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

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Recruitment Status

COMPLETED

Total Enrollment

40 participants

Study Classification

OBSERVATIONAL

Study Start Date

2012-09-30

Study Completion Date

2013-11-30

Brief Summary

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The purpose of the study is to assess changes in health-related quality of life in patients undergoing surgical correction of pectus carinatum. In addition, the study assessed long-term effects of surgical intervention in relation to the development of persistent postoperative pain and / or sensory disturbances in the surgical field.

Detailed Description

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Conditions

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Pectus Carinatum Quality of Life Pain, Postoperative Somatosensory Disorders

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Study Groups

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Pectus carinatum

Patients who have undergone surgical repair of pectus carinatum.

No interventions assigned to this group

Eligibility Criteria

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Inclusion Criteria

* all patients undergoing surgery for pectus carinatum

Exclusion Criteria

* patients without pectus carinatum
Minimum Eligible Age

10 Years

Maximum Eligible Age

55 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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University of Aarhus

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Locations

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Aarhus University Hospital, Skejby, Department of Cardiothoracic and Vacular Surgery

Aarhus, , Denmark

Site Status

Countries

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Denmark

Other Identifiers

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PECCAR-1

Identifier Type: -

Identifier Source: org_study_id

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