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Development, Field Testing and Evaluation of the Efficacy of a Hand-held, Portable and Affordable Thermo-coagulator to Prevent Cervical Cancer in Low- and Middle-income Countries (DELTA)

Primary Purpose

Cervical Precancer

Status
Active
Phase
Not Applicable
Locations
Zambia
Study Type
Interventional
Intervention
Thermocoagulation (device)
Cryotherapy (device)
LEEP (device)
Sponsored by
International Agency for Research on Cancer
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Cervical Precancer focused on measuring cervical precancer, screening, treatment, thermo-coagulation, thermal ablation, Reducing overtreatment

Eligibility Criteria

25 Years - 49 Years (Adult)FemaleDoes not accept healthy volunteers

Inclusion Criteria:

  • Positive on VIA test for cervical cancer screening
  • Eligible for ablative treatment

Exclusion Criteria:

  • Pregnancy
  • Not voluntarily willing to participate

Sites / Locations

  • UNC Global Project Zambia

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Experimental

Active Comparator

Active Comparator

Arm Label

Thermocoagulation (device)

Cryotherapy (device)

LEEP (device)

Arm Description

VIA Positive women will be treated by the new device for thermocoagulation

VIA positive women will be treated by cryotherapy

VIA Positive women not suitable for thermo-coagulation or cryotherapy will be treated by LEEP

Outcomes

Primary Outcome Measures

Difference in proportions with no lesions at 12 months follow-up between the thermocoagulation and cryotherapy arms among VIA positive women treated at baseline
The VIA positive women will be followed up after 12 months to see if the lesions have disappeared. HPV test will be used as the test of cure

Secondary Outcome Measures

Over-treatment defined as the number of VIA positive women found with no CIN lesions in the post-operative LEEP specimens
The LEEP specimens will be subjected to histopathology to check for presence of cervical intraepithelial neoplasias

Full Information

First Posted
September 6, 2016
Last Updated
March 2, 2023
Sponsor
International Agency for Research on Cancer
Collaborators
University of North Carolina Global Project Zambia, Liger Medical Llc
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1. Study Identification

Unique Protocol Identification Number
NCT02956239
Brief Title
Development, Field Testing and Evaluation of the Efficacy of a Hand-held, Portable and Affordable Thermo-coagulator to Prevent Cervical Cancer in Low- and Middle-income Countries
Acronym
DELTA
Official Title
Development, Field Testing and Evaluation of the Efficacy of a Hand-held, Portable and Affordable Thermo-coagulator to Prevent Cervical Cancer in Low- and Middle-income Countries
Study Type
Interventional

2. Study Status

Record Verification Date
March 2023
Overall Recruitment Status
Active, not recruiting
Study Start Date
August 1, 2017 (Actual)
Primary Completion Date
August 31, 2023 (Anticipated)
Study Completion Date
September 30, 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
International Agency for Research on Cancer
Collaborators
University of North Carolina Global Project Zambia, Liger Medical Llc

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
This project develops, tests and produces a lightweight, cordless, battery driven and rechargeable hand-held device for treating cervical precancer (Liger Thermal Coagulator). The study evaluates its effectiveness compared to the current standard treatment (cryocautery) when used as part of a screen and treat programme using Visual Inspection with Acetic acid (VIA) in Sub Saharan Africa.
Detailed Description
This project aims to improve screen and treat programmes for cervical cancers by discovering the best method of treatment. The specific aims are To develop, test and produce 20 novel lightweight hand-held cordless, portable battery driven and rechargeable Thermal Coagulators (Liger Medical, Utah). To evaluate the success / failure rate of Thermal Coagulation in a randomised controlled trial comparing thermal coagulation to the existing current standard cryocautery and to Large Loop Excision of the Transformation Zone (LLETZ aka LEEP) as part of a screen and treat programme in Zambia. To evaluate the user satisfaction scores of the Liger Thermal Coagulator cryocautery as part of a screen and treat programme in Zambia. To determine the rate of over treatment of VIA positive women as revealed by histopathological examination of the randomly assigned excised treatment cases. To determine the value of Z scan to predict normality and abnormality in VIA positive women randomly assigned to excisional therapy In collaboration with a medical devices company in Utah, the engineering performance of the Liger Thermal Coagulator has been developed and tested in vitro and in vivo. 200+ Liger units have been produced and a randomised controlled trial of the device has been undertaken, compared to cryocautery and LLETZ using efficacy and user friendliness as endpoints. The inclusion of a study arm of excisional therapy allows to quantify the rate of overtreatment in VIA programmes and using the Z scan may allow for a non invasive method of accurately predicting normality and abnormality in VIA positive women.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Cervical Precancer
Keywords
cervical precancer, screening, treatment, thermo-coagulation, thermal ablation, Reducing overtreatment

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
450 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Thermocoagulation (device)
Arm Type
Experimental
Arm Description
VIA Positive women will be treated by the new device for thermocoagulation
Arm Title
Cryotherapy (device)
Arm Type
Active Comparator
Arm Description
VIA positive women will be treated by cryotherapy
Arm Title
LEEP (device)
Arm Type
Active Comparator
Arm Description
VIA Positive women not suitable for thermo-coagulation or cryotherapy will be treated by LEEP
Intervention Type
Procedure
Intervention Name(s)
Thermocoagulation (device)
Intervention Description
Thermocoagulation uses heat injury to destroy the abnormal dysplastic cells of the cervix
Intervention Type
Procedure
Intervention Name(s)
Cryotherapy (device)
Intervention Description
Cryotherapy uses cold injury to destroy the abnormal dysplastic cells of the cervix
Intervention Type
Procedure
Intervention Name(s)
LEEP (device)
Intervention Description
The abnormal area of the cervix is excised with a thin metallic loop driven by electrosurgical unit
Primary Outcome Measure Information:
Title
Difference in proportions with no lesions at 12 months follow-up between the thermocoagulation and cryotherapy arms among VIA positive women treated at baseline
Description
The VIA positive women will be followed up after 12 months to see if the lesions have disappeared. HPV test will be used as the test of cure
Time Frame
12 months
Secondary Outcome Measure Information:
Title
Over-treatment defined as the number of VIA positive women found with no CIN lesions in the post-operative LEEP specimens
Description
The LEEP specimens will be subjected to histopathology to check for presence of cervical intraepithelial neoplasias
Time Frame
12 months

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
25 Years
Maximum Age & Unit of Time
49 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Positive on VIA test for cervical cancer screening Eligible for ablative treatment Exclusion Criteria: Pregnancy Not voluntarily willing to participate
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Partha Basu, Dr
Organizational Affiliation
IARC
Official's Role
Principal Investigator
Facility Information:
Facility Name
UNC Global Project Zambia
City
Lusaka
Country
Zambia

12. IPD Sharing Statement

Plan to Share IPD
Yes
Citations:
PubMed Identifier
31734069
Citation
Pinder LF, Parham GP, Basu P, Muwonge R, Lucas E, Nyambe N, Sauvaget C, Mwanahamuntu MH, Sankaranarayanan R, Prendiville W. Thermal ablation versus cryotherapy or loop excision to treat women positive for cervical precancer on visual inspection with acetic acid test: pilot phase of a randomised controlled trial. Lancet Oncol. 2020 Jan;21(1):175-184. doi: 10.1016/S1470-2045(19)30635-7. Epub 2019 Nov 14.
Results Reference
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PubMed Identifier
34197624
Citation
Mwanahamuntu M, Kapambwe S, Pinder LF, Matambo J, Chirwa S, Chisele S, Basu P, Prendiville W, Sankaranarayanan R, Parham GP. The use of thermal ablation in diverse cervical cancer "screen-and-treat" service platforms in Zambia. Int J Gynaecol Obstet. 2022 Apr;157(1):85-89. doi: 10.1002/ijgo.13808. Epub 2021 Jul 31.
Results Reference
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Development, Field Testing and Evaluation of the Efficacy of a Hand-held, Portable and Affordable Thermo-coagulator to Prevent Cervical Cancer in Low- and Middle-income Countries

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