Cryotherapy vs. LEEP to Treat CIN2/3 Among HIV-positive Women (PHE-LEEP)
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Purpose
The purpose of this study is to compare the rate of recurrence of cervical intraepithelial neoplasia among HIV-positive women receiving cryotherapy versus LEEP over 2 years of follow-up and to compare the shedding of HIV-1 from the cervix between HIV-positive women receiving cryotherapy versus LEEP over 6 weeks of follow-up.
| Condition | Intervention |
|---|---|
|
Cervical Intraepithelial Neoplasia |
Procedure: Loop Electrosurgical Excision Procedure (LEEP) Procedure: Cryotherapy |
| Study Type: | Interventional |
| Study Design: | Allocation: Randomized Endpoint Classification: Efficacy Study Intervention Model: Parallel Assignment Masking: Open Label Primary Purpose: Treatment |
| Official Title: | Impact of Cryotherapy Versus Loop Electrosurgical Excision Procedure (LEEP) on Recurrence of Cervical Intraepithelial Neoplasia and HIV-1 Cervical Shedding Among HIV-positive Women |
- recurrence of cervical intraepithelial neoplasia among HIV-positive women [ Time Frame: 2 years ] [ Designated as safety issue: No ]Rate of recurrence of cervical intraepithelial neoplasia among HIV-positive women receiving cryotherapy versus LEEP over 2 years of follow-up
- Shedding of HIV-1 from the cervix between HIV-positive women [ Time Frame: 6 weeks ] [ Designated as safety issue: No ]Shedding of HIV-1 from the cervix between HIV-positive women receiving cryotherapy versus LEEP over 6 weeks of follow-up
| Estimated Enrollment: | 400 |
| Study Start Date: | April 2011 |
| Estimated Study Completion Date: | April 2014 |
| Estimated Primary Completion Date: | April 2014 (Final data collection date for primary outcome measure) |
| Arms | Assigned Interventions |
|---|---|
|
Experimental: Cryotherapy
Cryotherapy procedure which will freeze and remove the diseased part of the cervix
|
Procedure: Cryotherapy
Cryotherapy procedure which will freeze and remove the diseased part of the cervix
|
|
Experimental: Loop Electrosurgical Excision Procedure (LEEP)
LEEP procedure uses a heated wire to scoop out disease from the cervix
|
Procedure: Loop Electrosurgical Excision Procedure (LEEP)
LEEP procedure uses a heated wire to scoop out disease from the cervix
Other Name: LEEP
|
Detailed Description:
The recent scale-up of antiretroviral treatment programs in resource-limited settings provides an unprecedented opportunity to implement a comprehensive cervical cancer screening and treatment program for women who, by virtue of having HIV, are at significant risk for cervical disease. Unfortunately, even if screening is offered free of charge to millions of women living with HIV, it is unclear which treatment modality for pre-cancerous cervical lesions will be most effective since HIV appears to affect outcomes of treatment by increasing the recurrence and severity of cervical disease. Cervical treatment may also increase shedding of HIV from the cervix which may put discordant couples at risk and possibly spread HIV more widely. This study proposes to randomize HIV-positive women with cervical intraepithelial neoplasia grade 2 and 3 (CIN 2 and 3) to cryotherapy vs. loop electrosurgical excision procedure (LEEP) and measure the recurrence of cervical disease in each group over 2-years of follow-up as well as HIV shedding from the cervix for 6 weeks after treatment.
Our hypothesis is that compared to cryotherapy, LEEP is significantly more likely to prevent recurrence of cervical lesions over 2 years of follow-up and less likely to cause shedding of HIV-1 from the cervix over 2 months of follow-up.
Eligibility| Ages Eligible for Study: | 18 Years and older |
| Genders Eligible for Study: | Female |
| Accepts Healthy Volunteers: | No |
Inclusion Criteria:
- HIV positive receiving care at the Coptic Hope Center
- Not pregnant by clinical examination or history
- Have an intact cervix
- Have not received prior cervical treatment
- Do not have a history of a bleeding disorder
- Are above 18 years of age
Exclusion Criteria:
- HIV-negative
- Male
- Below 18 years of age
- Pregnant by clinical examination or history
- Post-hysterectomy
- Post-cervical cancer treatment.
Contacts and Locations| Kenya | |
| Coptic Hospital | Recruiting |
| Nairobi, Kenya, 21570-00505 | |
| Contact: Dr. Nelly Yatich yatich@u.washington.edu | |
| Principal Investigator: | Michael Chung, MD | University of Washington |
More Information
No publications provided
| Responsible Party: | Michael Chung, Assistant Professor, University of Washington |
| ClinicalTrials.gov Identifier: | NCT01298596 History of Changes |
| Other Study ID Numbers: | 35995-A, KE.09.0238 |
| Study First Received: | February 16, 2011 |
| Last Updated: | November 28, 2012 |
| Health Authority: | Kenya: Ethical Review Committee United States: Institutional Review Board |
Additional relevant MeSH terms:
|
Neoplasms HIV Seropositivity Cervical Intraepithelial Neoplasia Carcinoma in Situ HIV Infections Lentivirus Infections Retroviridae Infections RNA Virus Infections |
Virus Diseases Sexually Transmitted Diseases, Viral Sexually Transmitted Diseases Immunologic Deficiency Syndromes Immune System Diseases Carcinoma Neoplasms, Glandular and Epithelial Neoplasms by Histologic Type |
ClinicalTrials.gov processed this record on May 22, 2013