Trial · NCT04819867
Comparison Of The Effect Of Propolis And Gluma Desensitizer On The Management Of Dentin Hypersensitivity
NCT04819867, Phase 2, Phase 3, Completed, Dow University of Health Sciences
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. Comparison Of The Effect Of Propolis And Gluma Desensitizer On The Management Of Dentin Hypersensitivity. Trials, record NCT04819867. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT04819867
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Comparison Of The Effect Of Propolis And Gluma Desensitizer On The Management Of Dentin Hypersensitivity
- NCT number
- NCT04819867
- Status
- Completed
- Phases
- Phase 2, Phase 3
- Enrollment
- 40 participants, actual
- Lead sponsor
- Dow University of Health Sciences
- Conditions
- Dentin Hypersensitivity
- Interventions
- Propolis, Gluma Desensitizer
- First posted
- 2021-03-29
- Last updated
- 2021-03-29
Source ClinicalTrials.gov
Registered outcomes16
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | treatment of dentin hypersensitivity | baseline reading will be taken on VAS At day 0 then propolis will be applied. | management of dentin hypersensitivity |
| Primary | treatment of dentin hypersensitivity | reading on VAS will be taken immediately after application of Propolis on day 0 | management of dentin hypersensitivity |
| Primary | treatment of dentin hypersensitivity | reading on VAS will be taken after 1 week of application Propolis | management of dentin hypersensitivity |
| Primary | treatment of dentin hypersensitivity | reading on VAS will be taken after 1 month of application of Propolis | management of dentin hypersensitivity |
| Primary | treatment of dentin hypersensitivity | baseline reading will be recorded on Schiff sensitivity score on day 0, then Propolis will be applied | management of dentin hypersensitivity |
| Primary | treatment of dentin hypersensitivity | reading will be recorded on Schiff sensitivity score on day 0, immediately after application of Propolis | management of dentin hypersensitivity |
| Primary | treatment of dentin hypersensitivity | reading will be recorded on Schiff sensitivity score 1 week after application of Propolis | management of dentin hypersensitivity |
| Primary | treatment of dentin hypersensitivity | reading will be recorded on Schiff sensitivity score 1 month after application of Propolis | management of dentin hypersensitivity |
| Primary | treatment of dentin hypersensitivity | baseline reading will be taken on VAS at day 0, before application of Gluma desensitizer | management of dentin hypersensitivity |
| Primary | treatment of dentin hypersensitivity | reading will be taken on VAS at day 0, immediately after application of Gluma desensitizer | management of dentin hypersensitivity |
1 to 10 of 16Source ClinicalTrials.gov
See all 16 registered outcomesOutcomes0
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.
| PMID | Listed as |
|---|---|
| 38783427 | DERIVED |
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.
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/NCT04819867
GET https://conductscience.org/api/trials/v1/NCT04819867/registered