Study of Anal Cytologies in Patients With High Grade Cervical Intraepithelial Neoplasia (CIN II and III)

Sponsor
Universidade do Vale do Sapucai (Other)
Overall Status
Unknown status
CT.gov ID
NCT03241680
Collaborator
(none)
80
1
4
9.9
8.1

Study Details

Study Description

Brief Summary

Cervical cancer is the third most frequent neoplasm in Brazilian women (estimated risk of 15.33 cases / 100,000 women by 2014), behind breast and colorectal cancer.

This high incidence is explained by the pre-neoplastic lesions of the cervix being probably related to the practice of unsafe sex and to a poor local immune response against HPV.

Human papillomavirus (HPV) infection affects people of any age, although it is more common in young people, probably due to increased sexual activity in that period.

The association between high-risk HPV and anus neoplasm in men and women with immunodeficiency or immunosuppression has been confirmed and measures related to surveillance are standardized.

In patients without immunodeficiencies, this association is still unclear, which may contribute to the lack of adequate standards to diagnose HPV and prevent cancer of the anus.

The frequency of the cancer of anus previously considered low, is currently in considerable elevation, mainly squamous cell carcinoma (SCC).

The causal relationship between this virus and cancer of the cervix and the anus is established. These facts have motivated the inclusion of this disease as STD, which justifies the necessity of adopting surveillance measures in the clinics of sexual, gynecological and urological diseases.

Cancer of the anus, when diagnosed in the early stage, makes healing possible with less aggressive treatments, but in the advanced stage, abdominoperineal amputation is necessary.

Concerned about possible anal cancer, some gynecologists have referred patients with genital HPV to search for anal infection.

Condition or Disease Intervention/Treatment Phase
  • Diagnostic Test: Search of anal citology alterations
N/A

Study Design

Study Type:
Interventional
Anticipated Enrollment :
80 participants
Allocation:
Non-Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Prevention
Official Title:
Study of Anal Cytologies in Patients With High Grade Cervical Intraepithelial Neoplasia (CIN II and III)
Actual Study Start Date :
Aug 2, 2017
Anticipated Primary Completion Date :
Apr 30, 2018
Anticipated Study Completion Date :
May 31, 2018

Arms and Interventions

Arm Intervention/Treatment
No Intervention: Control Group with conventional citology

Patients who do not have high grade cervical intraepithelial neoplasia and will have anal cytology performed by conventional method

No Intervention: Control Group with liquid based citology

Patients who do not have cervical intraepithelial neoplasia of high grade and will have anal cytology performed by liquid based method

No Intervention: CIN 2-3/Conventional Citology

Patients with high grade cervical intraepithelial neoplasia and will have anal citology performed by conventional method

Active Comparator: CIN 2-3/Liquid Based

Patients with high grade cervical intraepithelial neoplasia and will have anal citology performed by liquid based method

Diagnostic Test: Search of anal citology alterations
All patients with a pathological diagnosis of CIN II and III, and in the general gynecological surgery outpatient clinic, will be selected at the outpatient clinic of Oncology Gynecology of the HCSL for a period of six months. Patients who meet the eligibility criteria will be clarified about the study, and only those who agree to participate will be included, by signing the informed consent form (TCLE).

Outcome Measures

Primary Outcome Measures

  1. Study of Anal Cytologies in Patients With High Grade Cervical Intraepithelial Neoplasia (CIN II and III) [Six months]

    Search for alterations in the anal cytology of patients with CIN 2-3 in conventional and liquid based anal citology

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 65 Years
Sexes Eligible for Study:
Female
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:

Female patients aged 18-65 years with an anatomic pathology compatible with CIN II / CIN III, without restriction regarding skin color, race, ethnicity, religion; Patients of the Oncology Gynecology Service of the HCSL, registered in the hospital management system, in outpatient consultations; Those who agree to participate in the study and sign the ICF. Patients attended at the general gynecological surgery outpatient clinic (control group) with no evidence of colpocitological alteration.

-

Exclusion Criteria:

Patients who withdraw the consent term. History of previous anal cancer / anal intraepithelial neoplasia. Immunosuppressed: HIV, SLE, users of immunosuppressive and transplanted drugs.

-

Contacts and Locations

Locations

Site City State Country Postal Code
1 Lyliana C R Barbosa Pouso Alegre MG Brazil 37550000

Sponsors and Collaborators

  • Universidade do Vale do Sapucai

Investigators

  • Study Chair: Daniela F Veiga, Vale do Sapucai University

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Lyliana Coutinho Resende Barbosa, MD Phd, Universidade do Vale do Sapucai
ClinicalTrials.gov Identifier:
NCT03241680
Other Study ID Numbers:
  • Citologia anal
First Posted:
Aug 7, 2017
Last Update Posted:
Aug 7, 2017
Last Verified:
Aug 1, 2017
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Aug 7, 2017