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Trial · NCT04699383

Documentation of Patient Outcomes for SSG/Allopurinol Combination Treatment in Ethiopia

NCT04699383, Completed, Institute of Tropical Medicine, Belgium

3 sourcestrials-2026-11-12-0.4.0

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ConductScience Library. Documentation of Patient Outcomes for SSG/Allopurinol Combination Treatment in Ethiopia. Trials, record NCT04699383. Release trials-2026-11-12-0.4.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT04699383

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Trial

As registered on ClinicalTrials.gov, in the graph's capture of the registry.

Title
Documentation of Patient Outcomes for SSG/Allopurinol Combination Treatment in Ethiopia
NCT number
NCT04699383
Status
Completed
Enrollment
105 participants, actual
Lead sponsor
Institute of Tropical Medicine, Belgium
Conditions
Cutaneous Leishmaniasis
Interventions
Sodium Stibogluconate with allopurinol
First posted
2021-01-07
Last updated
2024-03-18

Source ClinicalTrials.gov

Registered outcomes6

Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.

ListOutcomeTime frameDescription
PrimaryTreatment outcome at day 180 (proportion with cure, good response, poor response, no response and relapse)day 180
cure defined as 100% flattening and/or reepithelization, good response 50-99% flattening and/or reepithelization, poor response 1-49% flattening and/or reepithelization, no response 0% flattening and/or reepithelization and relapse as worsening of existing lesion or appearance of new lesions
SecondaryPatient reported outcomes using the dermatology life quality index (DLQI)day 0 - day 180Mean difference in Dermatology life quality index (min 0, max 30) before treatment and at day 180
SecondarySide-effectsday 0 - day 180Proportion of patients with side-effects and proportion of side-effects according to CTCAE severity grades
SecondaryCycles to cureday 0 - day 180Number of cycles needed to reach cure
SecondaryFactors associated with cureday 30, day 180To determine covariate-adjusted risk ratios for baseline and follow-up factors associated with cure after one cycle of treatment and at the end of cycle 5
SecondaryTreatment outcome at day 30 (proportion with cure, good response, poor response, and no response )day 30
cure defined as 100% flattening and/or reepithelization, good response 50-99% flattening and/or reepithelization, poor response 1-49% flattening and/or reepithelization, no response 0% flattening and/or reepithelization

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.

Papers1

The papers the trial lists on ClinicalTrials.gov.

PMIDListed as
37624352RESULT

Source PubMed

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.

Source

Release
trials-2026-11-12-0.4.0
Release manifest SHA-256
0f4a8d8c48aee2a7573ae0fa94ecbeab70c1adbe449bbc95c424bc7d3e97b9d4
Registry capture
2026-11-12
Results copy, AACT
2026-03-23
NIH clinical studies file
2026-11-13

Source ClinicalTrials.gov

Sources 3

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNone 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/NCT04699383

GET https://conductscience.org/api/trials/v1/NCT04699383/registered