Success of Implant Restorations After Immediate or Delayed Implant Placement With/Without Ridge P… (NCT05988281) | Clinical Trial Compass
Not Yet RecruitingNot Applicable
Success of Implant Restorations After Immediate or Delayed Implant Placement With/Without Ridge Preservation
75 participantsStarted 2023-09
Plain-language summary
The study aims to compare clinical, radiographic, patient-reported outcomes (PROMs) and cost analysis outcomes in type I, II and socket preserved sites (III/IV) implant placement at 1-year post-loading in all groups.
Who can participate
Age range23 Years
SexALL
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Inclusion Criteria:
i) Patient must have willingness to read and sign a copy of the Informed Consent Form Males and females, ≥23 years old.
ii) Patient in need of a single permanent tooth extraction with clinical and/or radiographic evidence of unrestorable maxillary premolars, canines, or incisors with at least one adjacent tooth present, and with periodontal attachment preserved at least for two thirds of the root not associated with acute periapical pathology.
iii) Post-extraction alveolar bone defect with ≤50 % buccal bone loss. This will be confirmed at Visit 2 after extraction. In case of \>50% buccal bone loss, the participant will be withdrawn from the study.
iv) Patient in good general health as documented by self-assessment. v) Full mouth bleeding and plaque scores (FMBS \<10% and FMPS \<30%) recorded within the previous 8 weeks.
Exclusion Criteria:
i) Uncontrolled or untreated periodontal disease. ii) History of local (head and neck) radiation therapy. iii) Presence of oral lesions in the area of the extraction (such as ulceration, malignancy).
iv) Severe bruxing or clenching habits. v) Acute endodontic lesion in the test tooth or in the neighbouring areas to the extraction procedure (sites with presence of an asymptomatic chronic lesion are eligible).
vi) Medical history that includes uncontrolled diabetes or hepatic or renal disease, or other serious medical conditions that can impact on bone metabolism (e.g. rheumatoid arthritis, osteoporosis) or transmi…
What they're measuring
1
Combined success rate criteria.
Timeframe: 12 months after delivery of implant restoration.
Trial details
NCT IDNCT05988281
SponsorHospital General Universitario Morales Meseguer