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Treatment Time Comparing Digital & Conventional Workflows

Not Applicable
Completed
Conditions
Dental Implant
Interventions
Procedure: Treatment of implant single crown
Registration Number
NCT05165563
Lead Sponsor
Mahidol University
Brief Summary

This randomized controlled trial (RCT) analyzed monolithic single-unit implant restorations out of lithium disilicate (LS2) or polymer-infiltrated ceramic networks (PICN) in a chairside digital workflow (Test) and a conventional protocol (Control). The primary outcome was to investigate the treatment time of the overall operation. The null hypothesis of this RCT was that both workflows had comparable results with respect to the defined outcomes.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
40
Inclusion Criteria
  • The participants having a transmucosal implant system (Straumann TL RN/WN, Institut Straumann, AG, Basel, Switzerland) were placed in a single-tooth gap in the area of premolar or molar regions in the maxilla and mandible with existing interproximal and antagonist contacts.
  • general medical health is healthy or has a well-controlled systemic disease.
  • general oral health has shown no sign of infection or unsuccessfully treated diseases such as chronic periodontitis.
Exclusion Criteria
  • smoking more than 10 cigarettes per day.
  • pregnancy.
  • psychiatric disorder
  • history of radiation therapy at the head and neck area.
  • history of chemotherapy.
  • history of bony pathologies such as osseous dysplasia, odontogenic cyst or tumor, etc.

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
WorkflowsTreatment of implant single crownDigital and conventional workflows for treatment of implant single crowns
MaterialsTreatment of implant single crownMaterials for treatment of implant single crowns (polymer-infiltrated ceramic networks, PICNs and lithium disilicate, LS2).
Primary Outcome Measures
NameTimeMethod
Treatment timeFirst visit to prosthesis delivery visit, through study completion, an average of 1 month

Treatment time in every steps were recorded.

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Faculty of dentistry, Mahidol University

🇹🇭

Bangkok, Thailand

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