Trial · NCT07882745
This Feasibility Study Will Evaluate the Study Protocols for Treatment and Follow-up Controls of Primary Molars With Caries in Children Treated With Stainless Steel Crowns or Conventional Fillings. Treatment Success and Potential Failures Will be Followed at 3, 6 and 12 Months Post Treatment.
NCT07882745, Not applicable, Not yet recruiting, Marie Norman
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. This Feasibility Study Will Evaluate the Study Protocols for Treatment and Follow-up Controls of Primary Molars With Caries in Children Treated With Stainless Steel Crowns or Conventional Fillings. Treatment Success and Potential Failures Will be Followed at 3, 6 and 12 Months Post Treatment. Trials, record NCT07882745. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT07882745
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
This Feasibility Study Will Evaluate the Study Protocols for Treatment and Follow-up Controls of Primary Molars With Caries in Children Treated With Stainless Steel Crowns or Conventional Fillings. Treatment Success and Potential Failures Will be Followed at 3, 6 and 12 Months Post Treatment.
- NCT number
- NCT07882745
- Status
- Not yet recruiting
- Phases
- Not applicable
- Enrollment
- 100 participants, estimated
- Lead sponsor
- Marie Norman
- Conditions
- Dental Caries, Early Childhood Caries (ECC)
- Interventions
- Stainless steel crowns, Conventional fillings
- First posted
- 2026-10-20
- Last updated
- 2026-10-20
Source ClinicalTrials.gov
Registered outcomes6
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Parents and dentists' acceptance of study protocols assessed qualitatively in semi-structured interviews. | Interviews will start after the 12 month follow-up controls and will take approximately 3 months to complete and analyze. | All participating dentists and 5 parents from each treatment arm will be invited to take part in semi-structured interviews where acceptance of study protocols will be investigated qualitatively through semi-structured interviews. |
| Primary | Time for recruitment of participants to the study | Time for recruitment will be assessed as soon as 100 participants are enrolled in the study, estimated 1 year after the recruitment of participants starts. | The time it takes to recruit 100 participants from recruitment of participant nr 1 to participant nr 100. |
| Primary | Drop-out rate | From enrollment to the 12 months post treatment follow-up control | Number of participants who drop out of the study before the 12 months follow-up control. |
| Secondary | Tooth survival after 12 months | from start of treatment to end of last follow-up control 12 months post treatment | Incidence of tooth loss/extraction due to pain (pulpitis) or infection (apical periodontitis) at the 12 month follow-up control. |
| Secondary | Incidence of treated teeth in the study diagnosed with pain (pulpitis) or infection (apical periodontitis). | from start of treatment to end of last follow-up control 12 months post treatment | Incidence of treated teeth in the study diagnosed with pain (pulpitis) or infection (apical periodontitis) in treated tooth at folllow-up control visits or emergency visitis. Pain can be diagnosed clinically and infection can be diagnosed clinically or on radiographs. |
| Secondary | Incidence of loss of stainless steel crown or filling | From start of treatment to end of last follow-up control 12 months post treatment | Number of participants with loss of stainless steel crown or filling diagnosed clinically at follow-up visits or at emergency visits. |
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.
Papers5
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/NCT07882745
GET https://conductscience.org/api/trials/v1/NCT07882745/registered