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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: ClinicalTrials.gov
Last refreshed on: 19 February 2015
Main ID:  NCT00513123
Date of registration: 07/08/2007
Prospective Registration: No
Primary sponsor: M.D. Anderson Cancer Center
Public title: Measurement of Digital Colposcopy for Fluorescence Spectroscopy of Cervical Intraepithelial Neoplasia
Scientific title: A Pilot Study: Measurement of Digital Colposcopy for Fluorescence Spectroscopy of Cervical Intraepithelial Neoplasia
Date of first enrolment: September 2002
Target sample size: 100
Recruitment status: Completed
URL:  http://clinicaltrials.gov/show/NCT00513123
Study type:  Observational
Study design:  Observational Model: Case-Only, Time Perspective: Prospective  
Phase:  N/A
Countries of recruitment
Canada Nigeria United States
Contacts
Name:     Michele Follen, MD, PhD
Address: 
Telephone:
Email:
Affiliation:  M.D. Anderson Cancer Center
Key inclusion & exclusion criteria

Inclusion Criteria:

- Women 18 and older with an abnormal Pap

Exclusion Criteria:

- Pregnant individuals will be excluded from this study



Age minimum: 18 Years
Age maximum: N/A
Gender: Female
Health Condition(s) or Problem(s) studied
Cervical Cancer
Intervention(s)
Procedure: Colposcopy
Primary Outcome(s)
To study whether digital colposcopy for fluorescence (DCF) can perform better than standard methods to detect cancer of the cervix or precancerous lesions. [Time Frame: 7 Years]
Secondary Outcome(s)
Secondary ID(s)
GYN98-258
Source(s) of Monetary Support
Please refer to primary and secondary sponsors
Secondary Sponsor(s)
National Cancer Institute (NCI)
Ethics review
Results
Results available:
Date Posted:
Date Completed:
URL:
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