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MOVIDA 1 Ter - Evaluation of the Cobas® Plasma Separation Card in the Field in Vietnam (MOVIDA1-Ter)

Primary Purpose

HIV Infections

Status
Recruiting
Phase
Not Applicable
Locations
Vietnam
Study Type
Interventional
Intervention
Blood sampling
Sponsored by
Institut Pasteur
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional diagnostic trial for HIV Infections focused on measuring Viral Load Monitoring, Dried Blood Spot

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • ≥18 years of age
  • HIV-1 infected adults
  • Willing to participate to the study by giving his/her consent

Exclusion Criteria:

  • None

Sites / Locations

  • Dong Da
  • Nam Tu LiemRecruiting

Arms of the Study

Arm 1

Arm Type

Other

Arm Label

Blood Sampling

Arm Description

blood samples from venepuncture (10mL)

Outcomes

Primary Outcome Measures

Quantification of HIV RNA on DBS compared to plasma as gold standard
sensitivity and specificity of the Cobas® PSC against plasma (as gold standard) at to identify virological failure (HIV VL ≥1000 copies/mL)

Secondary Outcome Measures

Correlation between HIV RNA VL measured on DBS and on plasma
Comparison of quantitative HIV VL results obtained on plasma and when using the cobas® PSC

Full Information

First Posted
March 9, 2021
Last Updated
October 27, 2022
Sponsor
Institut Pasteur
Collaborators
National Institute of Hygiene and Epidemiology - Vietnam (NIHE)
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1. Study Identification

Unique Protocol Identification Number
NCT04794725
Brief Title
MOVIDA 1 Ter - Evaluation of the Cobas® Plasma Separation Card in the Field in Vietnam
Acronym
MOVIDA1-Ter
Official Title
Monitoring Of Viral Load In Decentralised Area 1 Ter - Evaluation of the Cobas® Plasma Separation Card in the Field in Vietnam
Study Type
Interventional

2. Study Status

Record Verification Date
October 2022
Overall Recruitment Status
Recruiting
Study Start Date
October 5, 2022 (Actual)
Primary Completion Date
October 2023 (Anticipated)
Study Completion Date
October 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Institut Pasteur
Collaborators
National Institute of Hygiene and Epidemiology - Vietnam (NIHE)

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
In low- and middle-income countries, viral load (VL) monitoring of patients living with HIV and followed on antiretroviral therapy (ART) in remote settings is still scarce. Barriers to VL monitoring are essentially the limited access to a laboratory able to perform this measurement, its cost, as well as the lack of human and material resources. Blood sampling using dried blood spots (DBS), which has been validated and is immediately available, could overcome these barriers. With DBS, transfer and conservation of samples are simplified enabling access to VL monitoring to patients seeking care in sites far from laboratory facilities. Use of DBS also offers the advantage not to require extensive investments. To guide decision makers in the implementation of strategies to scale-up HIV VL monitoring in remote settings, field evaluations of DBS in routine conditions are needed. It is in this context that we propose this field evaluation of the Cobas® plasma separation card in Vietnam
Detailed Description
In Vietnam, in 2018, HIV prevalence was estimated at 0.3% among adults and the estimated proportion of PLHIV on ART was 65%, however the HIV epidemic is essentially concentrated in people who inject drugs, men who have sex with men and sex workers. As of today, routine HIV VL monitoring is not yet available in remote settings in Vietnam. Despite an initiative we conducted and that documented the feasibility of DBS use in remote settings, and although no genuine roll-out of POC machines is yet observed in the field, the Ministry of Health of Vietnam has not yet decided to scale-up HIV VL monitoring using DBS. More field evaluations are needed to convince the Ministry of Health that DBS can effectively be used to scale-up HIV VL monitoring. The aim of the present study is to evaluate the sensitivity and specificity of HIV VL measurement using the cobas® plasma separation card (PSC) against plasma at the threshold of 1000 copies/mL (threshold currently used to define failure in Vietnam, following the WHO guidelines).

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
HIV Infections
Keywords
Viral Load Monitoring, Dried Blood Spot

7. Study Design

Primary Purpose
Diagnostic
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
250 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Blood Sampling
Arm Type
Other
Arm Description
blood samples from venepuncture (10mL)
Intervention Type
Procedure
Intervention Name(s)
Blood sampling
Intervention Description
blood samples from venepuncture (10mL)
Primary Outcome Measure Information:
Title
Quantification of HIV RNA on DBS compared to plasma as gold standard
Description
sensitivity and specificity of the Cobas® PSC against plasma (as gold standard) at to identify virological failure (HIV VL ≥1000 copies/mL)
Time Frame
up to 4 weeks
Secondary Outcome Measure Information:
Title
Correlation between HIV RNA VL measured on DBS and on plasma
Description
Comparison of quantitative HIV VL results obtained on plasma and when using the cobas® PSC
Time Frame
up to 4 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: ≥18 years of age HIV-1 infected adults Willing to participate to the study by giving his/her consent Exclusion Criteria: None
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Yoann MADEC, PhD
Phone
+33140613828
Email
yoann.madec@pasteur.fr
First Name & Middle Initial & Last Name or Official Title & Degree
Mohand AIT AHMED
Email
mohand.ait-ahmed@pasteur.fr
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Yoann MADEC, PhD
Organizational Affiliation
Institut Pasteur
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Tuan Anh NGUYEN, MD, PhD
Organizational Affiliation
National Institute of Hygiene and Epidemiology, Vietnam
Official's Role
Principal Investigator
Facility Information:
Facility Name
Dong Da
City
Hanoi
Country
Vietnam
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Tuan Anh NGUYEN, MD,PhD
Facility Name
Nam Tu Liem
City
Hanoi
Country
Vietnam
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Tuan Anh NGUYEN, MD, PhD

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
32271796
Citation
Nguyen TA, Tran TH, Nguyen BT, Pham TTP, Hong Le NT, Ta DV, Phan HTT, Nguyen LH, Ait-Ahmed M, Ho HT, Taieb F, Madec Y; MOVIDA 2 study group. Feasibility of dried blood spots for HIV viral load monitoring in decentralized area in North Vietnam in a test-and-treat era, the MOVIDA project. PLoS One. 2020 Apr 9;15(4):e0230968. doi: 10.1371/journal.pone.0230968. eCollection 2020.
Results Reference
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PubMed Identifier
29425216
Citation
Taieb F, Tran Hong T, Ho HT, Nguyen Thanh B, Pham Phuong T, Viet Ta D, Le Thi Hong N, Ba Pham H, Nguyen LTH, Nguyen HT, Nguyen TT, Tuaillon E, Delaporte E, Le Thi H, Tran Thi Bich H, Nguyen TA, Madec Y. First field evaluation of the optimized CE marked Abbott protocol for HIV RNA testing on dried blood spot in a routine clinical setting in Vietnam. PLoS One. 2018 Feb 9;13(2):e0191920. doi: 10.1371/journal.pone.0191920. eCollection 2018.
Results Reference
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MOVIDA 1 Ter - Evaluation of the Cobas® Plasma Separation Card in the Field in Vietnam

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