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Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT01551485
Other study ID # H-3-2011-022
Secondary ID
Status Active, not recruiting
Phase N/A
First received February 6, 2012
Last updated August 7, 2012
Start date February 2012
Est. completion date October 2012

Study information

Verified date August 2012
Source Rigshospitalet, Denmark
Contact n/a
Is FDA regulated No
Health authority Denmark: The Regional Committee on Biomedical Research Ethics
Study type Interventional

Clinical Trial Summary

Sleep after surgery has been found to be very distrubed immediately after major surgery. This is also seen after fast-track hip and knee replacement with length of stay of less than 3 days. Disturbed sleep has many adverse effects i.e. fatigue, possible hyperalgesia and decline in cognitive abilities.


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 20
Est. completion date October 2012
Est. primary completion date August 2012
Accepts healthy volunteers No
Gender Both
Age group 60 Years and older
Eligibility Inclusion Criteria:

- Total hip or knee replacement in fast-track setup

- Age 60 years or above

- ASA class 1-3

Exclusion Criteria:

- Anesthesia within the pas 30 days

- Daily use of alcohol > 21 units / week

- Use of anxiolytics or hypnotics within the past 30 days

- Inability to read and understand Danish

- Marked reduction of sight or hearing

- Parkinson's disease or other neurological disaese causing function deficits

- Inability to cooperate to sleep monitoring

- allergy to the drug tested

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Investigator)


Related Conditions & MeSH terms


Intervention

Drug:
Zolpidem
The effect of Zolpidem 10 mg for the first night after surgery is asssessed using PSG
Placebo
Pacebo tablet, blinded given on the first night after surgery

Locations

Country Name City State
Denmark Gentofte Hospital Gentofte

Sponsors (1)

Lead Sponsor Collaborator
Rigshospitalet, Denmark

Country where clinical trial is conducted

Denmark, 

Outcome

Type Measure Description Time frame Safety issue
Primary Change in sleep time on the first postoperative night compared to preoperatively. The primary endpoint is an evaluation of sleep stages on the first night postoperatively compared to preoperative measures for the same individual first night postoperatively - 24 hours No