ClinicalTrials.gg
RecruitingNCT06395129Updated Oct 9, 2026

Low Dead-space Injecting Equipment Distribution Program for People Who Inject Drugs in Low- and Middle-income Countries

An observational study in Drug Use, Hepatitis and Hiv, sponsored by Médecins du Monde. Recruiting at 9 sites in 3 countries. Open to participants aged 18 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-10-09.

Sponsored by Médecins du Monde · Observational

From the registry’s dates

  • Started Sep 2024; still recruiting 2 years 1 month later.
Updated Oct 9, 2026Primary completion movedStudy completion movedGo to Updates ↓
Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
2,400
Ages
18 Years and older
Sex
All
01

Study summary

Implementation and evaluation of a distribution program for low dead-space syringes/needles (LDSS/N) in Armenia, Georgia, and Tanzania, Egypt, Nigeria, Vietnam, India, Ukraine, and South Africa. This study aims to generate evidence on best practice LDSS/N distribution programs which will enhance acceptability and sustain high levels of LDSS/N uptake.

People who inject drugs and access needle and syringe programs will be invited to attend up to three focus group discussion rounds (with 25 participants in each focus group round) to inform and provide feedback on a concurrent distribution program of LDSS/N.

Throughout distribution, a cohort study will be run alongside distribution with 240 participants enrolled per country (with the exception of Nigeria, where 480 participants will be recruited) who will undergo HIV and HCV testing and answer surveys on their sociodemographic and behavioral status. Key informant interviews will also be held with participating staff and stakeholders to evaluate the feasibility and acceptability of this program.

Primary outcomes assessed through this study include 1) community values and preferences for LDSS/N, 2) barriers and facilitators to accessing LDSS/N, 3) feasibility and effectiveness of the distribution program on increasing LDSS/N uptake, 4) model the potential public health impact and cost effectiveness of LDSS/N distribution in this setting.

Read the detailed description

This study will recruit people who inject drugs to inform and evaluate the selection and distribution of low dead-space needles and syringes (LDSS/N) at their existing NSP services.

The interventions include: low- dead-space needles and syringes; and knowledge mobilisation through Focus Group Discussions (FGDs) and peer education.

Specifically, in Phase 1, people who inject drugs will be recruited at each study site to participate in FGDs, in which they will be presented with a selection of new LDSS/N products, provided information about their advantages regarding blood borne virus (BBV) transmission risk, and invited to discuss their values and preferences regarding needle- and syringe choice to inform the selection of LDSS/N to be piloted for scaled up distribution at their study sites.

Following the FGDs, during Phase 2 people who inject drugs who are registered clients at participating NSP services can enroll in a 6-week pilot period during which they will have access to a small selection of new LDSS/N products alongside the usual services they access at the study site or needle and syringe program (NSP). When the 6 week pilot phase concludes, participants will be invited to participate in a second round of FGDs, where they will be asked reflect on their experiences using the new LDSS/N products and share their opinions on which products to select for scaled up distribution to all clients accessing the study sites.

In Phase 3, a small selection LDSS/N (2-5) will be made available alongside the usual needles- and syringes and other existing harm reduction services at the study site/NSPs. During this period, two forms of data will be collected, 1) routine programmatic data, and 2) data from a concurrent cohort study.

The routine programmatic data collected will include information already routinely collected by the sites when individuals attend (site specific client ID, type and quantity of needles/syringes (N/S) collected) along with two additional questions 'Did you use a LDSS/N the last time you injected?" and "Thinking about the last week, for how many of your injections did you use a LDSS/N?'. No identifiable data will be recorded as part of routine programmatic data collection, therefore individuals included in this process are not considered 'participants' and will not undergo informed consent. This data will be used for the purposes of monitoring and evaluating LDSS/N uptake.

Alongside this distribution period, 240 people per country who inject drugs accessing participating study sites will be recruited into an observational cohort study. Participants will be asked to undergo HIV and HCV antibody testing and to answer surveys on demographic and behavioral activities at four timepoints (baseline, 6-months, 12-months, 18-months).

At the conclusion of the distribution period, a third round of FGDs will be run to assess the acceptability and impact of the LDSS/N distribution program. Key informant interviews with study staff and key stakeholders will also be completed to explore the feasibility and effectiveness of the LDSS/N program.

Following all data collection, mathematical modelling will estimate the impact and cost-effectiveness of scaling up LDSS/N for people who inject drugs at a country-level, including modelling the impact on BBV transmission.

02

Conditions studied

  • Drug Use
  • Hepatitis
  • Hiv

Keywords

  • Low dead-space needles and syringes
  • Qualitative interviews
  • LDSS/N
  • High dead space needles/syringes (HDSS/N)
  • Rapid diagnostic test (RDT)
  • Feasibility
  • Acceptability
  • Cost effectiveness
  • Modelling
  • Focus group discussions
  • Harm Reduction
  • Values and preferences
  • Needle and syringe exchange program
  • Blood borne virus
03

In context

Hepatitis

343 studies on the registry are indexed under Hepatitis; 51 are open to participants now.

This study's planned enrollment of 2,400 is above the median of 358 across 90 observational studies indexed under Hepatitis.

Browse Hepatitis studies →

Lead sponsor

Médecins du Monde is the lead sponsor of 3 studies on the registry; 2 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
Yes
Sampling method
Non-probability sample

Study population

People aged 18+ who report injecting drug use

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Aged ≥18 years (note that country-specific protocols may include participants aged ≥16 where appropriate and relevant);
  • Reporting a history of recent (past month) injection drug use;
  • Accessing the NSP to receive injecting equipment at either a facility, mobile service or through outreach and have an accompanying assigned program unique ID;
  • Able to understand and communicate in the local language(s);
  • If self-reporting / negative status, interested in and agreeing to undergo HCV and HIV testing; and
  • Willing and able to provide to take part in the study.

Exclusion criteria

Exclusion Criteria:

  • N/A
Terms in these criteria, in plain language(3)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

Hepatitis C tests

Hepatitis C is a virus that infects the liver. An HCV antibody test can stay positive after an infection has cleared (and is occasionally positive without one); an HCV RNA test shows whether the virus is there now.

After treatment, hepatitis C counts as cured when HCV RNA is still undetectable 12 weeks or more after the treatment ended. Studies often accept people cured this way.

HIV

The human immunodeficiency virus, which weakens the immune system.

Many studies now accept people whose HIV is controlled on treatment, judged by the viral load and the CD4 count. Check the limits this study sets.

Informed consent

Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.

You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.

05

Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
2,400 participants (estimated)
Patient registry
No

Groups and cohorts

  • Cohort study

    All participants in the cohort study will undergo surveys, HIV, and HCV testing at four possible timepoints (baseline, 6-months, 12-months, and if time permits 18-months). They will also have access to the study sites usual services, and the introduced LDSS/N.

    Device: Low dead-space syringes/needles · Device: Hepatitis C Antibody Rapid Diagnostic Test · Device: HIV rapid Diagnostic Test

Interventions

  • DeviceLow dead-space syringes/needles

    LDSS/N are a type of syringe/needle which retains less residual blood following an injecting event when compared to HDSS/N.

    Also known as: LDSS/N

  • DeviceHepatitis C Antibody Rapid Diagnostic Test

    Administered up to 4 times, at baseline, 6-months, 12-months, and 18-months

    Also known as: HCV RDT

  • DeviceHIV rapid Diagnostic Test

    Administered up to 4 times, at baseline, 6-months, 12-months, and 18-months

    Also known as: HIV RDT

06

What researchers measure

Primary outcomes

  1. Effectiveness of a community values and preferences informed LDSS/N distribution program on increasing LDSS uptake among people who inject drugs

    Defined as reported exclusive use of LDSS/N vs not exclusive use of LDSS/N

    Time frame: 18 months

Secondary outcomes

  1. Understanding community values and preferences for LDSS/N in the context of other harm reduction supplies available to people who inject drugs

    Identified through focus group discussions

    Time frame: 18 months

  2. Barriers and facilitators to access and uptake of LDSS/N among people who inject drugs

    Assessed through surveys and focus group discussions

    Time frame: 18 months

  3. Differences in blood borne virus (HIV/HCV) incidence between those who exclusively use LDSS/N and those who do not

    Time frame: 18 months

  4. Model the potential public health impact (HCV and HIV infections averted) and cost-effectiveness of LDSS/N distribution for people who inject drugs within harm reduction settings

    Time frame: 18 months

  5. Identifying the enablers and challenges affecting the supply chain for LDSS/N

    Time frame: 18 months

  6. Document the legal, social, and regularity enablers and challenges affecting the successful introduction and maintenance of LDSS/N distribution

    Time frame: 18 months

  7. Evaluate LDSS/N demand creation approaches

    Time frame: 18 months

07

Study locations

9 of 9 sites recruiting
  • Real World Real People
    Yerevan, Armenia
    Recruiting
  • Step to Future
    Gori, Georgia
    Recruiting
  • New Vector
    Rustavi, Georgia
    Recruiting
  • Hepa+
    Tbilisi, Georgia
    Recruiting
  • Mukikute
    Dar es Salaam, Tanzania
    Recruiting
  • Peer 2 Peer
    Dar es Salaam, Tanzania
    Recruiting
  • Yovaribe
    Ilala, Tanzania
    Recruiting
  • Mefada
    Kinondoni, Tanzania
    Recruiting
  • STEPS Tanzania
    Ubungo, Tanzania
    Recruiting
08

References and documents

Individual participant data

Plan to share: Undecided

No publications or documents are linked to this record.

09

Updates

1 registry update since Sep 25, 2026
Primary completion
Dec 2026→Nov 2027
Oct 9, 2026
Study completion
Dec 2026→Dec 2027
Oct 9, 2026
Show all 1 update
  1. Oct 9, 2026
    Primary completion Dec 2026→Nov 2027
    Study completion Dec 2026→Dec 2027
    + 1 other change: verification date

From the registry record's own update history. This site started tracking changes on Sep 25, 2026; for anything earlier, see the record history on ClinicalTrials.gov ↗

10

Registry details

Key details

Study ID
NCT06395129
Lead sponsor
Médecins du Monde
Collaborators
UNITAID, Burnet Institute, International Network of People who Use Drugs, University of Bristol, Frontline AIDS, Caritas, Drug-free and preventitve healthcare organisation Nigeria, National Viral Hepatitis and STI Control Program Nigeria, PATH, Population Services International, London School of Hygiene and Tropical Medicine
Responsible party
Sponsor
First posted
May 1, 2024
Start date
Sep 13, 2024
Primary completion
Nov 2027 (estimated)
Completion
Dec 2027 (estimated)
Last update
Oct 9, 2026

Study contacts

Bridget Draper
Contact
bridget.draper@burnet.edu.au
+61 413 272 698
Mark Stoové
Contact
mark.stoove@burnet.edu.au
Mark Stoové
principal investigator · Burnet

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
Yes
View the source record on ClinicalTrials.gov ↗

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