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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-IOR-14005556
Date of registration: 2014-11-26
Prospective Registration: Yes
Primary sponsor: Panyu central hospital of Guangzhou
Public title: The clinical research on the evaluation of tubal patency by three-dimensional B-ultrasound-radiography after different hemostasis methods of tubal-pregnancy conservative laparoscopy operation
Scientific title: The clinical research on the evaluation of tubal patency by three-dimensional B-ultrasound-radiography after different hemostasis methods of tubal-pregnancy conservative laparoscopy operation
Date of first enrolment: 2015-01-01
Target sample size: A:50;B:50;C:50;D:50;
Recruitment status: Pending
URL:  http://www.chictr.org.cn/showproj.aspx?proj=9939
Study type:  Interventional study
Study design:  Randomized parallel controlled trial  
Phase:  Other
Countries of recruitment
China
Contacts
Name: SU HUIMING   
Address:  NO.8, Fuyu east road, Shiqiao Street, Panyu District, Guangzhou, Guangdong 511400
Telephone: +86 13922319945
Email: suhuiok@126.com
Affiliation:  Panyu central hospital of Guangzhou
Name: SU HUIMING   
Address:  NO.8, Fuyu east road, Shiqiao Street, Panyu District, Guangzhou, Guangdong 511400
Telephone: +86 13922319945
Email: suhuiok@126.com
Affiliation: 
Key inclusion & exclusion criteria
Inclusion criteria: 1. Age: 20 to 40 years of age, with fertility requirements;
2. No bleeding or bleeding in the abdominal cavity, with stable vital signs;
3. beta-HCG in serum more than 2000 U/L;
4. Liver and kidney function and red blood cells, white blood cell and platelet counts were normal;
5. The preoperative diagnosis of ectopic pregnancy is clear, the function of vital organs is normal, no surgical contraindications;
6. The total condition of the patients is unfit for the research.

Exclusion criteria: 1. Significant internal hemorrhage, vital signs were unstable;
2. beta-HCG in serum less than or equal to 2000 U/L, the diameter of accessory less than at least 4cm, no significant bleeding, the patients who choose onservative therapy;
3. The patients who do not agree to enter clinical trials.


Age minimum: 18
Age maximum: 45
Gender: Female
Health Condition(s) or Problem(s) studied
tubal pregnancy
Intervention(s)
A:mono electrosurgery ;B:bipolar electrosurgery ;C:cut margin suture ;D:fallopian mesentery\uterus artery uplink branch ligature ;
Primary Outcome(s)
operation time;intraoperative blood loss;evaluation of tubal patency bythree-dimensional B-ultrasound-radiography;
Secondary Outcome(s)
Secondary ID(s)
Source(s) of Monetary Support
research fund of Panyu central hospital of Guangzhou
Secondary Sponsor(s)
Ethics review
Results
Results available:
Date Posted:
Date Completed:
URL:
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