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Main
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Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register. |
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Register:
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ChiCTR |
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Last refreshed on:
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18 April 2017 |
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Main ID: |
ChiCTR-OCC-14004533 |
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Date of registration:
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2014-04-16 |
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Prospective Registration:
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Yes |
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Primary sponsor: |
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Public title:
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The superior anesthetic management scheme during perioperative period for myasthenia gravis patients
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Scientific title:
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The superior anesthetic management scheme during perioperative period for myasthenia gravis patients |
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Date of first enrolment:
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2014-04-30 |
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Target sample size:
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volunteer:30;MG group:30; |
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Recruitment status: |
Completed |
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URL:
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http://www.chictr.org.cn/showproj.aspx?proj=5039 |
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Study type:
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Observational study |
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Study design:
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Case-Control study
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Phase:
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Other
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Countries of recruitment
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China
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Contacts
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Name:
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Cao Yingya
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Address:
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Wannan Medical College, The South Sliverlake Road, Wuhu,Anhui, China
241001
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Telephone:
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+86 15055324662 |
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Email:
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caoyingya1990@126.com |
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Affiliation:
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Wannan Medical College |
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Name:
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Lu Weihua
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Address:
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Yijishan Hospital, Wannan Medical College, The West Zheshan Road, Wuhu, Anhui, China
241001
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Telephone:
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+86 13955370637 |
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Email:
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lwh683@sohu.com |
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Affiliation:
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Wannan Medical College |
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Key inclusion & exclusion criteria
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Inclusion criteria: Experimental groups:
1) clinical and laboratory findings in line with myasthenia gravis diagnosis;
2) elective surgery;
3) older than 6 years old;
4) authorized by the patient or other family members own consent.
Control group:
1) clinical and laboratory findings do not meet the diagnosis of myasthenia gravis, and no nervous system, immune system and muscle disease history;
2) older than 6 years old;
3) the patient or other family members agreed to authorize their own.
Exclusion criteria: Patients who have one of the following should be excluded from the study:
1) patients with underlying reasons such as heart or lung illness or difficult airway anesthesia that lead to anesthesia or intubation impossible;
2) the patient or family members asked to leave;
3) the patient is participating in other clinical trials;
4) The researchers believe that other reasons were not suitable for clinical trials.
Age minimum:
10
Age maximum:
66
Gender:
Both
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Health Condition(s) or Problem(s) studied
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myasthenia gravis
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Intervention(s)
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volunteer:muscle relaxant monitor;MG group:muscle relaxant monitor;
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Primary Outcome(s)
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Muscle relaxant effect;complications;
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Source(s) of Monetary Support
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Anhui province Medical research program from Anhui health board (2010C066)
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Results
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Results available:
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Date Posted:
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Date Completed:
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URL:
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