Trial · NCT07903662
Registered outcomes12
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
1 to 12 of 12
Download this page as JSON| 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. |
| Secondary | Total invoiced treatment cost | Through completion of prosthetic treatment, an average of 6 weeks. | Total invoiced treatment cost per participant, in Swiss francs (CHF): invoiced prosthesis-related clinical services plus dental laboratory costs from treatment initiation to definitive insertion; unrelated dental services excluded. Restricted to participants treated in the specialist (non-student-course) setting. Reported separately per workflow. |
| Secondary | Estimated personnel-related process cost | Through completion of prosthetic treatment, an average of 6 weeks. | Estimated personnel-related process cost per participant, in Swiss francs (CHF): prospectively recorded active clinical and dental laboratory working times multiplied by predefined personnel cost rates (separate rates for clinical and dental laboratory time). Restricted to participants treated in the specialist (non-student-course) setting. Reported separately per workflow. |
Source ClinicalTrials.govtrials-2026-11-12-0.5.0
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 list from software.
Twenty rows a page, as JSON. No key.
GET https://conductscience.org/api/trials/v1/NCT07903662/registered