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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT02063152
Other study ID # 201305072RINC
Secondary ID
Status Recruiting
Phase N/A
First received February 10, 2014
Last updated August 14, 2017
Start date January 1995

Study information

Verified date August 2017
Source National Taiwan University Hospital
Contact Hui-Chi Chen, PhD
Phone +886 2 23910409
Email d90842001@ntu.edu.tw
Is FDA regulated No
Health authority
Study type Observational [Patient Registry]

Clinical Trial Summary

This study aimed to evaluate the subsequent cancer risks, including gynecological cancers and malignancies at other sites, after the detection of screening positives and the diagnosis for primary cervical cancer.


Recruitment information / eligibility

Status Recruiting
Enrollment 300000
Est. completion date
Est. primary completion date December 2020
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 20 Years to 130 Years
Eligibility Inclusion Criteria:

- Citizens in Taiwan

- Women who attended screening, or who were diagnosed as cervical cancer

- Women who did not attend screening for at least 6 years

Exclusion Criteria:

- Women died before the follow-up initiation

- Women who had received hysterectomy before the follow-up initiation

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
Taiwan Taiwan Cervical Cancer Prevention Monitoring Center Taipei

Sponsors (1)

Lead Sponsor Collaborator
National Taiwan University Hospital

Country where clinical trial is conducted

Taiwan, 

Outcome

Type Measure Description Time frame Safety issue
Primary Time to the cancer diagnosis or the recurrence, the death, or the last date of follow-up, whichever came first up to 25 years
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