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. |
Register:
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ChiCTR |
Last refreshed on:
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18 April 2017 |
Main ID: |
ChiCTR-OOB-15006039 |
Date of registration:
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2015-03-04 |
Prospective Registration:
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Yes |
Primary sponsor: |
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Public title:
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Prospective study on association between vaginal microbiota and the histocompatibility of transvaginal pelvic polypropylene mesh
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Scientific title:
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Association between vaginal microbiota and the histocompatibility of transvaginal pelvic polypropylene mesh |
Date of first enrolment:
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2015-03-05 |
Target sample size:
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preoperative group:30;postoperative group:30; |
Recruitment status: |
Recruiting |
URL:
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http://www.chictr.org.cn/showproj.aspx?proj=10504 |
Study type:
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Observational study |
Study design:
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historical control
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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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Zhibo Zhang
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Address:
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No.1, Shuaifuyuan, Dongcheng Destrict, Beijing
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Telephone:
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+86 13693317164 |
Email:
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zzbspace@126.com |
Affiliation:
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Peking Union Medical College Hospital |
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Name:
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Lan Zhu
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Address:
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No.1, Shuaifuyuan, Dongcheng Destrict, Beijing
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Telephone:
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+86 13911714696 |
Email:
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zhu_julie@vip.sina.com |
Affiliation:
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Key inclusion & exclusion criteria
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Inclusion criteria: Menopausal POP patients who have already accepted trans-vaginally placed mesh treatment.
Exclusion criteria: 1. Patients with Diabetes and the blood glucose is not controlled under the target level;
2. Patients with immunological diseases and have been taking glucocorticoid hormone or anti-immunolgical drugs regularly;
3. Patients who had taken antibiotics or antifungal disease in latest 30 days;
4. Patients who had sexual life, trans-vaginally placed drug or vaginal lavage in the past 48 hours;
5. Patients who had bacterial vaginosis or sexually transmitted disease.at the current visit;
6. Patients who had intrauterine device.
Age minimum:
Age maximum:
Gender:
Female
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Health Condition(s) or Problem(s) studied
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Pelvic organ prolapse
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Intervention(s)
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preoperative group:transvaginal polypropylene mesh surgery;postoperative group:transvaginal polypropylene mesh surgery;
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Primary Outcome(s)
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the structure and abundance of vaginal microbiota;
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Source(s) of Monetary Support
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Self-collected
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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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