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

Completed · Phase 3

Conditions studied: Cervical Intraepithelial Neoplasia

In brief

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

Key facts

Study ID

NCT00237562

Run by

University of California, Irvine

Starts

1999-07-01

Last updated by the study team

2006-05-05

Who can join

Age: 18 and older. Sex: female. Healthy volunteers: accepted.

You may qualify if…

• Older than 18 years
• No history of invasive cervical cancer
• Not pregnant

You may not qualify if…

• Absence of a cervix
• Abnormal vaginal bleeding
• Cervical cancer screening within the previous 12 months
• A known bleeding disorder
• Reluctance to be randomized
• Unwillingness to follow the study protocol

Where it is running

• University of California, Irvine — Orange, California, United States

Full record on ClinicalTrials.gov

Trial information comes from ClinicalTrials.gov and is refreshed daily. TrialsForMe does not provide medical care and does not run the studies it lists.