- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01231776
Acupuncture Improves Sleep in Patients Undergoing Cardiopulmonary Bypass
Study of Acupuncture of Traditional Chinese Medicine
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
60 patients are divided into three groups. control group: no any intervention; experiment group 1: acupuncture are used in patients before cardiac operation; experiment group 2: acupuncture are used through all the course in hospital.
before operation, before discharge, one month after operation, two month after operation, the quality of sleep are evaluated. and comparisons will be made in three groups.
Study Type
Enrollment (Anticipated)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Shaanxi
-
Xi'an, Shaanxi, China, 710032
- Enrolling by invitation
- Zhang Jinzhou
-
Xi'an, Shaanxi, China, 710032
- Recruiting
- Zhang Jinzhou
-
Contact:
- zhang jinzhou, MD
- Phone Number: 86-29-84771022
- Email: jinzhouzhang2006@yahoo.com
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- aging:18yr--65yr
- cardiopulmonary bypass
- NYHA ≤II and EF≥50%
- not illiterate person
Exclusion Criteria:
- neurological disease,mentality disorder
- abuse of alcohol
- long history of smoking
- sleep disorder before admitting to hospital
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Prevention
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
No Intervention: control group
|
applying a stimula on neiguang and shenmen through electronic acupuncture
|
Active Comparator: acupuncture preoperative
acupuncture before operation for one week
|
applying a stimula on neiguang and shenmen through electronic acupuncture
|
Active Comparator: acupuncture in hospital
acupuncture all the time in hospital
|
applying a stimula on neiguang and shenmen through electronic acupuncture
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
multiple monitoring for sleeping
Time Frame: 24 hours
|
24 hours
|
Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start
Primary Completion (Anticipated)
Study Completion (Anticipated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Estimate)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 20100926
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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