CompletedNot Applicable

A Non-Interventional Study to Document the Use of Straumann BLX Implants in Daily Dental Practice

Germany153 participantsStarted 2018-05-14

Plain-language summary

Prospective, multi-center, non-interventional observation to document the success and survival rates of Straumann BLX Implants used for tooth replacement in cleared indications up to 1 year after implant placement

Who can participate

Age range18 Years

SexALL

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * Patients seeking an implant supported restoration * all patients with conditions that are in accordance with the IFU * Patients must provide their informed consent for study participation and must be willing and able to attend control visits * Patients need to be at least 18 years old Exclusion Criteria: \-

What they're measuring

Implant success rate at one year post implant placement

Timeframe: 12 months follow-up period after implantation

Implant survival rate at one year post implant placement

Timeframe: 12 months follow-up period after implantation

Trial details

NCT IDNCT03613077

SponsorInstitut Straumann AG

Sponsor typeINDUSTRY

Study typeOBSERVATIONAL

Primary completion2020-02-02

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