Trial · NCT07894523
Clinical and Radiographic Evaluation of Dia-Root Bio MTA for Indirect Pulp Capping in Young Permanent Molars
NCT07894523, Not applicable, Recruiting, Tanta University
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. Clinical and Radiographic Evaluation of Dia-Root Bio MTA for Indirect Pulp Capping in Young Permanent Molars. Trials, record NCT07894523. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT07894523
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Clinical and Radiographic Evaluation of Dia-Root Bio MTA for Indirect Pulp Capping in Young Permanent Molars
- NCT number
- NCT07894523
- Status
- Recruiting
- Phases
- Not applicable
- Enrollment
- 20 participants, estimated
- Lead sponsor
- Tanta University
- Conditions
- MTA, Pulp Caping, Permanent Molars, Radiographic Evaluation
- Interventions
- Dia-Root Bio MTA Indirect Pulp Capping, MTA Plus Indirect Pulp Capping
- First posted
- 2026-10-26
- Last updated
- 2026-10-26
Source ClinicalTrials.gov
Registered outcomes3
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Cumulative Clinical Success Rate | 3 months, 6 months, and 9 months post-operative. | Binary clinical evaluation (Success/Failure) defined as the complete absence of clinical signs and symptoms of pulpal/periapical pathology: Absence of tenderness to percussion or mastication. Absence of gingival swelling, abscess, or fistulous tract. Absence of pathological tooth mobility. |
| Primary | Radiographic Success Rate and Dentin Bridge Formation | Baseline (immediate post-operative), 3 months, 6 months, and 9 months post-operative. | Radiographic evaluation on standardized digital periapical radiographs to verify: Presence/increase in newly formed tertiary dentin thickness under the capping material. Radiodensity changes of affected dentin at the pulpal floor. Complete absence of internal/external root resorption or periapical radiolucency. |
| Secondary | Early Postoperative Pain Intensity | 6 hours, 12 hours, 24 hours, and 48 hours post-procedure. | Postoperative pain self-reported by the child/parent using a standardized 4-point facial pain intensity rating scale categorized as: 1. No pain 2. Slight pain 3. Moderate pain 4. Severe pain |
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.
Papers2
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/NCT07894523
GET https://conductscience.org/api/trials/v1/NCT07894523/registered