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Feasibility of the Management of Severe Cervical Dysplasia in a Single Visit

Cervical Intraepithelial Neoplasia Clinical Trial

Official title:
Single Visit Cervical Cancer Prevention Program

Clinical Trial Summary

1. Implement a single-visit program (SVP) for cervix cancer prevention in clinics serving a multi-ethnic population of women;

2. Set up an efficient system for interpretation of Pap smears for patients in the SVP that will minimize waiting time;

3. Determine the follow-up rates and compare them between women assigned to the SVP and a usual care program (UCP);

4. Determine satisfaction and compare it between women assigned to the SVP and the UCP;

5. Determine the cost-effectiveness and compare it between the SVP and UCP

Clinical Trial Description

Women were recruited from underserved communities to participate in this single visit cervix cancer project. Large loop electrosurgical excision procedure (LEEP) was performed on SVP subjects with either a diagnosis of HGSIL/AGUS or suspicion of carcinoma. All other subjects with abnormal Papanicolaou smears were referred to our abnormal cytology clinics or received care in the community. ;

Study Design

Allocation: Randomized, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Prevention

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT00237562
Study type Interventional
Source University of California, Irvine
Contact
Status Completed
Phase Phase 3
Start date July 1999
View Details
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