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Clinical Trials/NL-OMON23463
NL-OMON23463
Completed
Not Applicable

Short implants in the posterior region; an evaluation after 10 years

niversity Medical Centre Groningen (Netherlands)0 sites70 target enrollmentTBD
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Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Not specified
Sponsor
niversity Medical Centre Groningen (Netherlands)
Enrollment
70
Status
Completed
Last Updated
2 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

Guljé FL, Raghoebar GM, Vissink A, Meijer HJA. Single crowns in the resorbed posterior maxilla supported by either 6-mm implants or by 11-mm implants combined with sinus floor elevation surgery: a 1-year randomized controlled trial. Eur J Oral Implantol 2014;7:247-255. Guljé FL, Raghoebar GM, Vissink A, Meijer HJA. Single crowns in the resorbed posterior maxilla supported by either 11-mm long implants combined with sinus floor elevation or by 6-mm long implants: a 5-year randomised controlled trial. Int J Oral Implantol 2019; 12: 315-326.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
2 years ago
Study Type
Interventional

Investigators

Sponsor
niversity Medical Centre Groningen (Netherlands)

Eligibility Criteria

Inclusion Criteria

  • •Patients referred to the department of Oral and Maxillofacial Surgery 10 years ago and treated with a short dental implant and an implant\-supported restoration because of having a missing tooth in the posterior region. At the time of treatment:
  • •The patient was 18 years or older;
  • •The missing tooth was a premolar or molar in maxilla or mandible;
  • •Sufficient healthy and vital bone to insert a dental implant with a minimum length of 6 mm and at least 4\.0 mm in diameter with initial stability \> 45 Ncm
  • •The implant site was free from infection;
  • •Adequate oral hygiene (modified plaque index and modified sulcus bleeding index \= 1\);
  • •Sufficient mesio\-distal, bucco\-lingual, and interocclusal space for placement of an anatomic restoration;
  • •The patient was capable of understanding and giving informed consent.

Exclusion Criteria

  • •Exclusion criteria at the time of treatment:
  • •Medical and general contraindications for the surgical procedures;
  • •Presence of an active and uncontrolled periodontal disease;
  • •A history of local radiotherapy to the head and neck region.

Outcomes

Primary Outcomes

Not specified

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