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Clinical Trials/DRKS00020224
DRKS00020224
Not Yet Recruiting
N/A

Interaction of temporary and definitive prosthetic materials for implant-suprastructures with the peri-implant soft-tissue (study part1) and longevity of implant-supported, monolithic zirconia crowns (study part 2): prospective, randomized pilot study

niversitätsklinikum Ulm0 sites20 target enrollmentJanuary 21, 2020

Overview

Phase
N/A
Intervention
Not specified
Conditions
K08.1
Sponsor
niversitätsklinikum Ulm
Enrollment
20
Status
Not Yet Recruiting
Last Updated
last year

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
January 21, 2020
End Date
TBD
Last Updated
last year
Study Type
Interventional
Sex
All

Investigators

Sponsor
niversitätsklinikum Ulm

Eligibility Criteria

Inclusion Criteria

  • Tooth space width at least 7 mm, allowing for an implant insertion before the study starts or as the case may be, state after two\-stage augmentation or internal sinus lift or one\-stage minor extent lateral Augmentation;
  • at least 2 mm gingival height;
  • legally competent patient with supply needs

Exclusion Criteria

  • Need for major extent lateral augmentation in a one\-stage procedure (meaning that two\-stage bone block surgery can be included as well as internal sinus lift or minor extent lateral augmentation)
  • Need for application of a soft tissue transplant
  • Implant insertion using a surgical template was impossible before the study starts
  • Tooth space width is smaller than 7 mm (The interdental papilla would be severed during punch biopsy in this case)
  • Less than 2 mm gingival height in the lowest most area
  • Lack of informed consent
  • Chronic diseases
  • Pregnancy
  • Alcohol\- or drug abusus
  • Anamnestic peculiarities, ruling out implant treatment before the study starts

Outcomes

Primary Outcomes

Not specified

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