Ignite Creation Date:
2024-05-05 @ 12:04 PM
Last Modification Date:
2024-10-26 @ 9:20 AM
Study NCT ID:
NCT00237562
Status:
COMPLETED
Last Update Posted:
2006-05-05
First Post:
2005-10-10
Brief Title:
Feasibility of the Management of Severe Cervical Dysplasia in a Single Visit
Sponsor:
University of California Irvine
Organization:
University of California Irvine
Study Overview
Official Title:
Single Visit Cervical Cancer Prevention Program
Status:
COMPLETED
Status Verified Date:
2005-10
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief 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
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
Detailed 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 HGSILAGUS 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 Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
None
Is a FDA Regulated Device?:
None
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None