Trial · NCT06265870
Specific Versus Empirical Anthelminthic Treatment in Eosinophilia
NCT06265870, Not applicable, Unknown, Prince of Songkla University
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. Specific Versus Empirical Anthelminthic Treatment in Eosinophilia. Trials, record NCT06265870. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT06265870
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Specific Versus Empirical Anthelminthic Treatment in Eosinophilia
- NCT number
- NCT06265870
- Status
- Unknown
- Phases
- Not applicable
- Enrollment
- 700 participants, estimated
- Lead sponsor
- Prince of Songkla University
- Conditions
- Eosinophilia
- Interventions
- Albendazole, Ivermectin or albendazole
- First posted
- 2024-02-20
- Last updated
- 2024-09-24
Source ClinicalTrials.gov
Registered outcomes2
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Eosinophilia recovery | From receive anthelminthic treatment to the end of treatment at 4 weeks | Recovery from eosinophilia was defined as an absolute eosinophil count of less than 500 cells per microliter, as measured from the complete blood count (CBC) four weeks after receiving anthelminthic treatment. |
| Secondary | Change in AEC | From receive anthelminthic treatment to the end of treatment at 4 weeks | Comparing the change in AEC from baseline between the \"specific treatment group\" and the \"empirical treatment group\" using either a paired t-test or the Wilcoxon signed-rank test. |
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.
Papers18
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/NCT06265870
GET https://conductscience.org/api/trials/v1/NCT06265870/registered