Trial · NCT07903662
Digital and Conventional Clasp-retained Partial Dentures (DIGICLASP)
NCT07903662, Not yet recruiting, University of Bern
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. Digital and Conventional Clasp-retained Partial Dentures (DIGICLASP). Trials, record NCT07903662. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT07903662
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Digital and Conventional Clasp-retained Partial Dentures (DIGICLASP)
- NCT number
- NCT07903662
- Status
- Not yet recruiting
- Enrollment
- 70 participants, estimated
- Lead sponsor
- University of Bern
- Conditions
- Partial Edentulism
- First posted
- 2026-10-29
- Last updated
- 2026-10-29
Source ClinicalTrials.gov
Registered outcomes12
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Cumulative active prosthesis-related clinical chairside time | From the first prosthesis-related appointment through definitive insertion, an average of 6 weeks per participant. | Cumulative active prosthesis-related clinical chairside time per participant, in minutes, summed across all treatment sessions from the first prosthesis-related appointment to definitive insertion. Includes regular clinical scanning required for fabrication, framework try-in and clinical adjustment, if required. Excludes waiting and interruption time, study-specific scanning procedures and framework planning/drawing. Reported separately for the digital and conventional fabrication workflows. |
| Secondary | Number of clinical appointments | Through completion of prosthetic treatment, an average of 6 weeks. | Number of clinical appointments per participant from the first prosthesis-related appointment to definitive insertion. Reported separately per workflow. |
| Secondary | Active dental laboratory technician time | From receipt of the laboratory order to completion of framework fabrication, approximately 3-4 weeks after treatment initiation. | Active dental laboratory technician working time per participant, in minutes, recorded for predefined fabrication steps; idle time between steps is excluded. Reported separately per workflow. |
| Secondary | Quantitative framework fit | At initial framework try-in, approximately 3-4 weeks after treatment initiation, before clinical adjustment. | Three-dimensional surface distance between supporting tooth/ridge surfaces and the framework fitting surface, in micrometers, in predefined measurement regions, based on superimposition of an intraoral scan without the framework, an intraoral scan with the seated framework and an extraoral scan of the finished framework. Continuous measure; no clinical cut-off. Reported separately per workflow. |
| Secondary | Number of participants whose framework meets all clinical fit and stability criteria before adjustment | At framework try-in, approximately 3-4 weeks after treatment initiation, before clinical adjustment. | Four predefined yes/no criteria: seating of rests; adaptation of clasps and tooth-contacting components; adaptation of the major connector; stability under bilateral finger pressure. Reported separately per workflow. |
| Secondary | Number of participants whose framework requires clinical adjustment | At framework try-in, approximately 3-4 weeks after treatment initiation. | Whether clinical adjustment of the framework is required (yes/no). Reported separately per workflow. |
| Secondary | Active clinical adjustment time | At framework try-in, approximately 3-4 weeks after treatment initiation. | Active clinical adjustment time per participant, in minutes, including participants without adjustment (0 minutes). Reported separately per workflow. |
| Secondary | Number of participants with clinically acceptable final framework fit | At completion of framework try-in, approximately 3-4 weeks after treatment initiation. | Number of participants whose framework demonstrates clinically acceptable final fit (yes/no), assessed after completion of framework try-in and clinical adjustment, if required. Reported separately per workflow. |
| Secondary | Number of participants whose framework requires laboratory rework | Through completion of prosthetic treatment, an average of 6 weeks. | Rework documented with predefined cause categories. Reported separately per workflow. |
| Secondary | Number of participants whose framework requires complete remake | Through completion of prosthetic treatment, an average of 6 weeks. | Remake documented with predefined cause categories. Reported separately per workflow. |
1 to 10 of 12Source ClinicalTrials.gov
See all 12 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.
Papers4
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/NCT07903662
GET https://conductscience.org/api/trials/v1/NCT07903662/registered