Trial · NCT06575647
Vivax Elimination With Tafenoquine (VET) Study
NCT06575647, Phase 4, Completed, Shoklo Malaria Research Unit
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. Vivax Elimination With Tafenoquine (VET) Study. Trials, record NCT06575647. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT06575647
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Vivax Elimination With Tafenoquine (VET) Study
- NCT number
- NCT06575647
- Status
- Completed
- Phases
- Phase 4
- Enrollment
- 1,242 participants, actual
- Lead sponsor
- Shoklo Malaria Research Unit
- Conditions
- Malaria, Malaria, Vivax, Plasmodium Vivax, Plasmodium Vivax Malaria
- Interventions
- Tafenoquine
- First posted
- 2024-08-28
- Last updated
- 2026-01-06
Source ClinicalTrials.gov
Registered outcomes4
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Incidence of Serious Adverse Events (SAEs) to assess safety and tolerability of Tafenoquine MDA | Baseline survey to end of Month-1 survey | Number of (serious) adverse events reported |
| Secondary | To compare the incidence by Rapid Diagnostic Test (RDT) of P. vivax before and 1-3-6 months after providing the single round of MDA with Tafenoquine radical cure treatment | Month 1, 3 and 6 | Malaria Incidence by RDT reported from malaria post at month 1, 3 and 6 |
| Secondary | To evaluate the adherence of healthcare workers to the SOP for implementing MDA of Tafenoquine. | Baseline survey and Month-1 survey | Proportion of village health workers adhere to the SOP for G6PD testing \& documentation, tafenoquine administration and adverse event recording \& reporting. |
| Secondary | To compare the prevalence by PCR of P. vivax before and a month after providing the single round of MDA. | Baseline survey and Month-1 survey | Difference in proportion positive to PCR positive before and a month after providing the single round of MDA. |
Source ClinicalTrials.gov
Outcomes0
Each outcome the trial posted results for, in ClinicalTrials.gov's words.
None in this release.
Results by group0
Each measurement the trial posted, group by group, in the words and numbers it posted.
None in this release.
Participant flow0
How many started, completed or left each group, period by period.
None in this release.
Adverse events0
Each adverse event the trial posted, group by group: the participants affected out of those at risk.
None in this release.
Adverse event totals0
The totals the trial posted for each group.
None in this release.
Papers4
The papers the trial lists on ClinicalTrials.gov.
Grants0
The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.
None in this release.
Trial comparisons0
Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.
None in this release.
Tests0
The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.
None in this release.
Data dates
The day each source was copied for this release.
Sources 3
- ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
- ClinicalTrials.govNo license stated
- NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
- ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
- ClinicalTrials.govnone stated
- NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)
ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
For software
Read this trial from software.
The record and each of its lists are JSON, twenty rows a page. No key.
GET https://conductscience.org/api/trials/v1/NCT06575647
GET https://conductscience.org/api/trials/v1/NCT06575647/registered