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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.
Register: ChiCTR
Last refreshed on: 18 April 2017
Main ID:  ChiCTR-OCC-14004533
Date of registration: 2014-04-16
Prospective Registration: Yes
Primary sponsor: Yijishan Hospital, Wannan Medical College, Wuhu 241001, China
Public title: The superior anesthetic management scheme during perioperative period for myasthenia gravis patients
Scientific title: The superior anesthetic management scheme during perioperative period for myasthenia gravis patients
Date of first enrolment: 2014-04-30
Target sample size: volunteer:30;MG group:30;
Recruitment status: Completed
URL:  http://www.chictr.org.cn/showproj.aspx?proj=5039
Study type:  Observational study
Study design:  Case-Control study  
Phase:  Other
Countries of recruitment
China
Contacts
Name: Cao Yingya   
Address:  Wannan Medical College, The South Sliverlake Road, Wuhu,Anhui, China 241001
Telephone: +86 15055324662
Email: caoyingya1990@126.com
Affiliation:  Wannan Medical College
Name: Lu Weihua   
Address:  Yijishan Hospital, Wannan Medical College, The West Zheshan Road, Wuhu, Anhui, China 241001
Telephone: +86 13955370637
Email: lwh683@sohu.com
Affiliation:  Wannan Medical College
Key inclusion & exclusion criteria
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
Health Condition(s) or Problem(s) studied
myasthenia gravis
Intervention(s)
volunteer:muscle relaxant monitor;MG group:muscle relaxant monitor;
Primary Outcome(s)
Muscle relaxant effect;complications;
Secondary Outcome(s)
Secondary ID(s)
Source(s) of Monetary Support
Anhui province Medical research program from Anhui health board (2010C066)
Secondary Sponsor(s)
Ethics review
Results
Results available:
Date Posted:
Date Completed:
URL:
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