Trial · NCT01072201
To Access the Effects of Mucositis in Adults With Dental Implants
NCT01072201, Phase 3, Completed, Colgate Palmolive; results first posted 2010-02-19
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. To Access the Effects of Mucositis in Adults With Dental Implants. Trials, record NCT01072201. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT01072201
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- To Access the Effects of Mucositis in Adults With Dental Implants
- NCT number
- NCT01072201
- Status
- Completed
- Phases
- Phase 3
- Enrollment
- 60 participants, actual
- Lead sponsor
- Colgate Palmolive
- Conditions
- Mucositis
- Interventions
- Triclosan and Fluoride, Fluoride
- First posted
- 2010-02-19
- Last updated
- 2010-10-05
- Results first posted
- 2010-02-19
Source ClinicalTrials.gov
Registered outcomes3
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Bleeding on Probing | 6 months | Percentage of Bleeding Scale: The bleeding sites are identified by either a 0 or 1. (0=no bleeding \& 1= bleeding) The number of spots between teeth that bleed are divided by number of spots between teeth that are scored. |
| Primary | Mean Pocket Depth | 6 Months | Measurement scale: 0 millimeter measurement= no pocket depth. 3, 4, 5, \& 6 millimeter are indications of deeper Pocket depth. |
| Primary | Mean Percentage of Plaque Scores | 6 Months | Mean Percentage (%) of dental plaque on all tooth surfaces, including implants and natural teeth. Plaque Scale is 0=no plaque and 1= dental plaque present. Percentage is derived from sum of all plaque scores divided by the number of tooth surfaces scored. |
Source ClinicalTrials.gov
Outcomes3
Each outcome the trial posted results for, in ClinicalTrials.gov's words.
| Type | Outcome | Time frame | Population | Units | Measured as |
|---|---|---|---|---|---|
| PRIMARY | Bleeding on Probing | 6 months | Percentage of bleeding sites | MEAN | |
| PRIMARY | Mean Pocket Depth | 6 Months | Millimeters | MEAN | |
| PRIMARY | Mean Percentage of Plaque Scores | 6 Months | percentage of dental plaque | MEAN |
Source ClinicalTrials.gov
Results by group6
Each measurement the trial posted, group by group, in the words and numbers it posted.
| Outcome | Group | Category | Value | Spread | Units |
|---|---|---|---|---|---|
| Bleeding on Probing | Total Toothpaste | 53.8 | Standard Deviation 17.6 | Percentage of bleeding sites | |
| Bleeding on Probing | Ultrabrite Toothpaste | 52.3 | Standard Deviation 24.6 | Percentage of bleeding sites | |
| Mean Pocket Depth | Total Toothpaste | 4.4 | Standard Deviation 0.6 | Millimeters | |
| Mean Pocket Depth | Ultrabrite Toothpaste | 4.5 | Standard Deviation 0.5 | Millimeters | |
| Mean Percentage of Plaque Scores | Total Toothpaste | 13.2 | Standard Deviation 15.6 | percentage of dental plaque | |
| Mean Percentage of Plaque Scores | Ultrabrite Toothpaste | 16.0 | Standard Deviation 17.8 | percentage of dental plaque |
Source ClinicalTrials.gov
Participant flow6
How many started, completed or left each group, period by period.
| Period | Milestone | Group | Participants | Units counted |
|---|---|---|---|---|
| Overall Study | STARTED | Total Toothpaste | 30 | |
| Overall Study | STARTED | Ultrabrite Toothpaste | 30 | |
| Overall Study | COMPLETED | Total Toothpaste | 30 | |
| Overall Study | COMPLETED | Ultrabrite Toothpaste | 29 | |
| Overall Study | NOT COMPLETED | Total Toothpaste | 0 | |
| Overall Study | NOT COMPLETED | Ultrabrite Toothpaste | 1 |
Source ClinicalTrials.gov
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 totals6
The totals the trial posted for each group.
| Total | Group | Affected | At risk |
|---|---|---|---|
| Total, all-cause mortality | Total Toothpaste | ||
| Total, all-cause mortality | Ultrabrite Toothpaste | ||
| Total, other adverse events | Total Toothpaste | 0 | 30 |
| Total, other adverse events | Ultrabrite Toothpaste | 0 | 29 |
| Total, serious adverse events | Total Toothpaste | 0 | 30 |
| Total, serious adverse events | Ultrabrite Toothpaste | 0 | 29 |
Source ClinicalTrials.gov
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 comparisons1
Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.
| Comparison |
|---|
| Total Toothpaste vs Ultrabrite Toothpaste: serious adverse events |
Source Trial comparisons
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/NCT01072201
GET https://conductscience.org/api/trials/v1/NCT01072201/registered