Clinical Trials Directory

Trials / Withdrawn

WithdrawnNCT01313104

Colposcopy and High Resolution Anoscopy in Screening For Anal Dysplasia in Patients With Cervical, Vaginal, or Vulvar Dysplasia or Cancer

Pilot Project for Anal Dysplasia Screening in Women With Cervical or Vulvar Dysplasia

Status
Withdrawn
Phase
N/A
Study type
Interventional
Enrollment
0 (actual)
Sponsor
Northwestern University · Academic / Other
Sex
Female
Age
18 Years
Healthy volunteers
Not accepted

Summary

This clinical trial studies colposcopy and high resolution anoscopy in screening for anal dysplasia in patients with cervical, vaginal, or vulvar dysplasia or cancer. Screening may help doctors find cancer cells early and plan better treatment for cancer

Detailed description

OBJECTIVES: I. To evaluate the risk of anal dysplasia in women with cervical or vulvar dysplasia. OUTLINE: Patients undergo colposcopy and cervical Papanicolaou test with Human papillomavirus (HPV) test followed by anal Papanicolaou test and high resolution anoscopy. Patients with dysplastic anal lesions undergo repeat anoscopy at 3, 9, 15, and 24 months. Patients with normal anoscopy are followed up at 1 and 2 years.

Conditions

Interventions

TypeNameDescription
PROCEDUREcolposcopyUndergo colposcopy
OTHERcervical Papanicolaou testUndergo cervical Pap smear
PROCEDUREscreening methodUndergo anal Pap smear
PROCEDUREscreening methodUndergo high resolution anoscopy

Timeline

First posted
2011-03-11
Last updated
2012-06-11

Source: ClinicalTrials.gov record NCT01313104. Inclusion in this directory is not an endorsement.