Skip to main content
MedPathMedPath Home
Clinical Trials/DRKS00028965
DRKS00028965
Recruiting
未知

Randomized controlled trial to compare the clinical performance of two self-adhesive resin cements when used with a fiber post and core build-up in endodontically treated teeth - SARC-Fiber post

3M Deutschland GmbH0 sites72 target enrollmentMarch 2, 2023
Share to TwitterShare to FacebookShare to LinkedInShare to Reddit

Overview

Phase
未知
Intervention
Not specified
Conditions
Not specified
Sponsor
3M Deutschland GmbH
Enrollment
72
Status
Recruiting
Last Updated
last year
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
March 2, 2023
End Date
TBD
Last Updated
last year
Study Type
Interventional
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • •1 Subject is at least 18 or older at time of consent.
  • •2 Subject is able to provide their own informed consent.
  • •3 Subject is willing to return for follow\-up examination for at least 5 years
  • •4 Subject needs an indirect crown or 3\-unit bridge restoration
  • •5 Subject has a tooth with one or less cavity walls of the anatomical crown remaining
  • •6 Subject’s tooth has a residual root canal thickness at the orifice of more than 1 mm
  • •7 Subject’s tooth is symptom free with a root canal filling without a radiologically visible periapical lesion.
  • •8 Subject’s tooth has the possibility to prep a 2 mm ferrule
  • •9 Subject’s tooth has a minimum of 8 mm post length within the root canal, with a minimum of 4 mm apical root canal filling
  • •10 Subject’s tooth has no or treated periodontitis with maximum probing depth of 4 mm and no bleeding on probing

Exclusion Criteria

  • •1 Subject has a known allergies to acrylate\-based materials or hydroperoxide
  • •2 Subject is enrolled in another clinical trial at the time of screening that would interfere with this study
  • •3 Subject’s tooth is aimed to serve as telescopic crown abutment.
  • •4 Subjects is in the opinion of the Investigator unsuitable for enrollment in this study for reasons not specified in the exclusion criteria
  • •5 Subject does not sign the informed consent form

Outcomes

Primary Outcomes

Not specified

Similar Trials

Not yet recruiting
Not Applicable
Comparison of ciprofloxacin ear drops and boric acid ear drops in active mucosal chronic otitis mediaHealth Condition 1: H661- Chronic tubotympanic suppurative otitis media
CTRI/2021/03/031647oknayak hospital
Completed
Not Applicable
A clinical trial to study to compare the outcomes of Calcaneal Fractures operated with Minimally Invasive Surgery(MIS) technique with conventional techniques of ORIF using Extensile lateral approach.Health Condition 1: null- calcaneal fractureHealth Condition 2: S920- Fracture of calcaneus
CTRI/2015/04/005704PGIMER21
Recruiting
Not Applicable
Randomized controlled clinical trial of comparison between block-type collagenated bone substitute versus particle type bone substitute in guided bone regeneration on horizontal ridge defect around dental implants
KCT0005348Yonsei University Health System, Dental Hospital70
Not yet recruiting
Phase 3
A study to compare clinical performance of new filling material with standard filling material in milk teeth with decayHealth Condition 1: K029- Dental caries, unspecified
CTRI/2020/11/028944Manipal College of Dental Sciences Manipal
Not yet recruiting
Phase 2
A clinical study to evaluate the effect of local ayurvedic application in umbilical cord care.
CTRI/2022/12/048635Tilak Ayurved Mahavidyalaya ,Pune