- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01393236
Heart Rate Variability During Sleep After Fast-track Surgery
December 13, 2011 updated by: Lene Krenk
Based on prior findings concerning sleep disturbances, in particular REM sleep disturbances, after fast-track hip and knee arthroplasty (H-2-2010-011) we performed a supplemental analysis of heart rate variablity after arousals during sleep.
We compared preoperative and postoperative results.
Study Overview
Status
Completed
Conditions
Study Type
Observational
Enrollment (Actual)
10
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
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Copenhagen, Denmark
- Rigshospitalet
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Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
60 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Sampling Method
Probability Sample
Study Population
We selected patients undergoing fasttrack hip and knee arthoplasty in fast-track setip.
The underwent sleep monotoring for 1 preoperative night and continously during hospitalisation, and for 1 night at home after surgery.
Description
Inclusion criteria (for the control group):
- Age > 60 years
Exclusion criteria:
- surgery within the last 2 months
- known sleep disorder (eg. sleep apnea)
- daily beta blocker treatment
- daily dopamine treatment
This protocol only concentrates on the healthy controls for the patient described in H-2-2010-011.
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
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patients
patient characteristics are specified in H-2-2010-011
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controls
age matched to patients described in protocol H-2-2010-011
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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heart rate variability
Time Frame: 24 hours
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heart rate variability measured 5 beats before arousel and 15 beats after arousel in different sleep stages.
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24 hours
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Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
July 1, 2011
Primary Completion (Actual)
December 1, 2011
Study Completion (Actual)
December 1, 2011
Study Registration Dates
First Submitted
July 11, 2011
First Submitted That Met QC Criteria
July 12, 2011
First Posted (Estimate)
July 13, 2011
Study Record Updates
Last Update Posted (Estimate)
December 14, 2011
Last Update Submitted That Met QC Criteria
December 13, 2011
Last Verified
December 1, 2011
More Information
Terms related to this study
Other Study ID Numbers
- H-2-2010-011a
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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