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Postoperative Sleep Disturbances After Fast Track Hip and Knee Replacement

Sponsor
Rigshospitalet, Denmark (Other)
Overall Status
Completed
CT.gov ID
NCT01144130
Collaborator
Lundbeck Center for Fast-Track Hip and Knee Replacement (Other)
10
Enrollment
1
Location
5
Duration (Months)
2
Patients Per Site Per Month

Study Details

Study Description

Brief Summary

The purpose of this study is to quantify the degree of sleep disturbances after hip or knee replacement surgery.

Through polysomnographic monitoring the disturbances in sleep stages will be clarified.

Condition or Disease Intervention/Treatment Phase

    Study Design

    Study Type:
    Observational
    Actual Enrollment :
    10 participants
    Time Perspective:
    Prospective
    Official Title:
    Postoperative Sleep Disturbances After Fast Track Hip and Knee Replacement
    Study Start Date :
    May 1, 2010
    Actual Primary Completion Date :
    Sep 1, 2010
    Actual Study Completion Date :
    Oct 1, 2010

    Outcome Measures

    Primary Outcome Measures

    1. Duration of REM sleep before and first postoperative night []

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    60 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:

    • above 60

    • ASA classification I-IV

    Exclusion Criteria:

    • general anaesthesia within 90 days

    • daily use of sedatives

    • alcohol abuse

    • insufficient written and verbal Danish

    • severe hearing loss and poor sight

    • Parkinsons Disease or other functional neurological deficits

    • Mini mental status < 24

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Hvidovre Hospital Hvidovre Denmark

    Sponsors and Collaborators

    • Rigshospitalet, Denmark
    • Lundbeck Center for Fast-Track Hip and Knee Replacement

    Investigators

    • Principal Investigator: Lene Krenk, Doctor, Rigshospitalet, Denmark

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    , ,
    ClinicalTrials.gov Identifier:
    NCT01144130
    Other Study ID Numbers:
    • H-2-2010-011
    First Posted:
    Jun 15, 2010
    Last Update Posted:
    Sep 20, 2011
    Last Verified:
    Oct 1, 2010
    Additional relevant MeSH terms:
    Dyssomnias
    Parasomnias

    Study Results

    No Results Posted as of Sep 20, 2011