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Clinical Trials/DRKS00007809
DRKS00007809
Completed
未知

Clinical Trial on Soft-Tissue Management for Conventional Dental Impressions - Part 2 - WGM II

niversitätsklinikum Ulm, Zentrum für Zahn-, Mund- und Kieferheilkunde, Klinik für Zahnärztliche Prothetik0 sites40 target enrollmentFebruary 16, 2015

Overview

Phase
未知
Intervention
Not specified
Conditions
K08.9
Sponsor
niversitätsklinikum Ulm, Zentrum für Zahn-, Mund- und Kieferheilkunde, Klinik für Zahnärztliche Prothetik
Enrollment
40
Status
Completed
Last Updated
last year

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
February 16, 2015
End Date
December 13, 2017
Last Updated
last year
Study Type
Interventional
Sex
All

Investigators

Sponsor
niversitätsklinikum Ulm, Zentrum für Zahn-, Mund- und Kieferheilkunde, Klinik für Zahnärztliche Prothetik

Eligibility Criteria

Inclusion Criteria

  • Eligible participants are between 18 and 80 years of age and do not suffer of any chronic or acute infection or disease. Female participants must not be pregnant. Also, there must be no alcohol or drug abusus.
  • Participants should not have known allergies against the materials used in this trial (astrigens, anesthesia, impression material). The periodontal screening index (PSI) has to be equal to or below 2 (no periodontal disease, at the most little calculus on the inside of the lower front teeth).
  • Both premolars and their neighboring teeth are present in the I. and II. quadrant of the upper jaw.
  • Premolars and their neighboring teeth are either healthy or flawlessly restored with circularly at least 1 mm supragingivally located restoration margins. These teeth must not be restored with crowns.

Exclusion Criteria

  • All participants who do not meet the inclusion criteria. Participants who are not fully legally competent. Participants where \- if necessary \- a short\-term restoration of carious lesions according to the following criteria is not possible.
  • Participants with inlays, onlays, partial crowns on teeth 3 to 6 (canine to first molar) of the upper jaw, if restoration margins are not located at least 1 mm supragingival.
  • Participants with crowns on teeth 3 to 6 of the upper jaw with equi\- or subgingival margins.

Outcomes

Primary Outcomes

Not specified

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