A randomised controlled trial of cytological surveillance versus patient choice between surveillance and colposcopy in managing mildly abnormal cervical smears

Not Applicable

Completed

• Conditions: Cancer (neoplasms): Cervix; Cancer; Malignant neoplasm of cervix uteri

• Registration Number: ISRCTN14634238
• Lead Sponsor: Record Provided by the NHS R&D 'Time-Limited' National Programme Register - Department of Health (UK)

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2004-01-23
• Last Update Posted: 17 October 2016

Recruitment & Eligibility

• Status: Completed
• Sex: Female
• Target Recruitment: 476

Inclusion Criteria

Women with mildly abnormal cervical smears

Exclusion Criteria

Pregnancy or abnormal vaginal bleeding.

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
ot provided at time of registration

Secondary Outcome Measures

Name	Time	Method
ot provided at time of registration