Trial · NCT02547727
Immune Responses After a Four-site Intradermal Rabies Booster Vaccination in HIV-infected Adults
NCT02547727, Not applicable, Unknown, Queen Saovabha Memorial Institute
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. Immune Responses After a Four-site Intradermal Rabies Booster Vaccination in HIV-infected Adults. Trials, record NCT02547727. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT02547727
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Immune Responses After a Four-site Intradermal Rabies Booster Vaccination in HIV-infected Adults
- NCT number
- NCT02547727
- Status
- Unknown
- Phases
- Not applicable
- Enrollment
- 40 participants, estimated
- Lead sponsor
- Queen Saovabha Memorial Institute
- Conditions
- Rabies
- Interventions
- rabies vaccine
- First posted
- 2015-09-11
- Last updated
- 2022-04-29
Source ClinicalTrials.gov
Registered outcomes3
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Rabies neutralizing antibody titers | Change from baseline of geometric mean titres of rabies neutralizing antibody titres at 2 weeks | Rabies neutralizing antibody titers would be represented and compared by geometric mean titers (GMTs) |
| Secondary | Specific T cell response | Change from baseline of percentages of rabies-antigen specific CD4+ T cells at 2 weeks | Specific T cell response is measured by OX-40 assay |
| Secondary | Cytokines assessment | Change from baseline of cytokines levels at 1 week | A few cytokines levels are measured by multiplex bead array assay |
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/NCT02547727
GET https://conductscience.org/api/trials/v1/NCT02547727/registered