A Comparison of Immediate Treatment of CIN1 With Cryotherapy and 12 Month Cytology Follow up in HIV Seropositive Women

U

University of Witwatersrand

Status

Unknown

Conditions

Cervical Dysplasia

Treatments

Procedure: cryotherapy

Study type

Interventional

Funder types

Other

Identifiers

NCT02250716
CIN1

Details and patient eligibility

About

Based on the high incidence of cervical cancer and high grade dysplasia and increased progression and incomplete treatment of CIN2 and 3 in South Africa, we propose to study the effect of cryotherapy among HIV-positive women diagnosed with CIN 1 versus regular 12 month cytology follow-up. This study will be a dual-arm, open-label, randomized clinical trial for HIV-infected women diagnosed with CIN 1 and receiving care at the Themba Lethu Clinic, Helen Joseph Hospital, Johannesburg, South Africa. CIN 1 will be identified from patients who have had a colposcopic biopsy for persistent LSIL as per standard of care.

Full description

Women with HIV have a higher risk of cervical cancer. Screening and treatment formaly of the disease is limited die to poor access of screening programs and multiple visits. Women with HIV also have high progressions rates of disease amd my need to be treated earliers. Cryotherapy is a low option and very easy to implement especially in low resource provinces. It is cheaper and easier to administer than Large Loop electrosurgical excision procedure (LLETZ) No histology or transportation costs of specimens Less invasive than LLETZ It is nurse driven and easily learned It decreases loss to follow-up of patients due to reduced waiting time, transportation costs, time off work and HIV stigma

Enrollment

480 estimated patients

Sex

Female

Ages

18 to 65 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • HIV -infected women whose biopsy proves CIN1 and who consent to study participants and procedures
  • CIN1 with no visible lesion
  • The entire ectocervical lesion should cover less than 75% of the cervix and not more than 2 - 3mm into the endocervical canal

Exclusion criteria

  • Pregnant women
  • Known and previous treatment for HSIL by any method (Cryotherapy, LEEP or cone biopsy)
  • Women who are menstruating or who have active pelvic inflammatory disease will be deferred from the study until the infection is cleared or the menstrual cycle has ended; the patient may then participate in the study.
  • Unsatisfactory colposcopic examination defined as inability to see the extent of the lesion in the endocervical canal and lesions deemed ineligible for cryotherapy by an OB/GYN specialist.
  • Previous hysterectomy with removal of the cervix

Trial design

480 participants in 2 patient groups

Arm 1
Experimental group
Description:
Immediate treatment with Cryotherapy and 12 month cytology and histology follow-up
Treatment:
Procedure: cryotherapy
Arm 2
No Intervention group
Description:
12 month cytology and histology follow-up

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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