Trial · NCT06251739
Repurposing Ivermectin for PKDL Treatment
NCT06251739, Early phase 1, Completed, International Centre for Diarrhoeal Disease Research, Bangladesh
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. Repurposing Ivermectin for PKDL Treatment. Trials, record NCT06251739. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT06251739
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Repurposing Ivermectin for PKDL Treatment
- NCT number
- NCT06251739
- Status
- Completed
- Phases
- Early phase 1
- Enrollment
- 30 participants, actual
- Lead sponsor
- International Centre for Diarrhoeal Disease Research, Bangladesh
- Conditions
- Post-kala-azar Dermal Leishmaniasis
- Interventions
- Ivermectin 6 Mg Oral Tablet, Miltefosine Oral Capsule
- First posted
- 2024-02-09
- Last updated
- 2025-09-10
Source ClinicalTrials.gov
Registered outcomes4
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Parasitological clearance | Within 12 months after treatment completion | PCR in Skin samples will be negative for LD-bodies in all the Ivermectin-treated patients |
| Primary | Lesion Reduction | Within 12 months after treatment completion | 90 % change of PKDL lesions in patients treated with Ivermectin |
| Secondary | No Severe Adverse Events | Within 3 months following enrollment | No Severe Adverse Events recorded in any of the patients treated with Ivermectin |
| Other | Side effects of Ivermectin | Within 3 months following enrollment | Determine the side effects of Ivermectin when administered in multiple doses |
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.
Papers0
The papers the trial lists on ClinicalTrials.gov.
None in this release.
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/NCT06251739
GET https://conductscience.org/api/trials/v1/NCT06251739/registered