Guided Bone Regeneration of Peri-implant Defects Comparing Submerged Versus Non-submerged Healing

Ana Molina Villar36 enrolled

Overview

Objective: the objective of the present randomized clinical trial is to compare changes in radiographic peri-implant bone defect fill after regeneration of peri-implant intrabony defects with a submerged versus a non-submerged protocol. Material and Methods: this project is a randomized controlled clinical trial, double blind, with a parallel groups design. Thirty-six patients presenting with peri-implantitis subsidiary of regenerative treatment will be recruited. After subjects have been given informed consent, they will be randomized to test or control group. All patients will undergo a session of non-surgical peri-implantitis therapy consisting on prostheses removal and implant debridement with ultrasounds, curettes and air-abrasive under local anaesthesia. Patients in test group will have their prostheses removed and the mucosa surrounding the affected implants will be let heal covering the implants, while patients in control group will have their prostheses installed again after the non-surgical therapy. Six to eight weeks later, all subjects will undergo regenerative treatment with the use of a bone substitute, a collagen membrane and fixation pins, and in control group tissues will heal following the non-submerged protocol, meanwhile subjects in test group will undergo submerged healing. Six months later, subjects in test group will have their prostheses reconnected to the regenerated implants. All patients will undergo periodontal and peri-implant maintenance therapy every three months during follow-up. Radiographic assessment of vertical bone level changes (primary outcome), clinical status of peri-implant tissues, changes in soft tissues margin, patient related outcomes and adverse events will be assessed at 3, 6 and 12 months after peri-implantitis regenerative surgery.

Study Type

INTERVENTIONAL

Allocation

RANDOMIZED

Purpose

TREATMENT

Masking

DOUBLE

Enrollment

Eligibility

Sex: ALLMin age: 18 YearsHealthy volunteers:

Medical Language ↔ Plain English

Inclusion Criteria: * Patients diagnosed of peri-implantitis requiring surgical therapy * The periapical radiographic study demonstrates an intra-bony component greater than 3 mm at the affected implant * There is at least 2 mm of keratinized mucosa around the affected implant * Intrasurgically, peri-implant defects must be type Ia, Ib, Ic and Ie (according to Schwarz et al. 2007) * Affected implants must be two-piece implants to allow for the submerged protocol * Affected implant supported restorations must be screw-retained or cemented, and should allow for prostheses removal Exclusion Criteria: * Patients with untreated periodontitis * Medical conditions requiring prolonged use of steroids and/or medications that can interfere with bone metabolism * Metabolic disorders such as osteoporosis * History of uncontrolled endocrine disorders * History of leukocyte dysfunction and deficiencies * History of immunodeficiency syndromes * History of neoplastic disease requiring the use of radiation of chemotherapy * History of renal failure * Physical handicaps that would interfere with the ability to perform adequate oral hygiene * Alcoholism or drug abuse * Smokers of more than 10 cigarettes per day, cigar equivalents or tobacco chewers * Any other condition or circumstance that, in the opinion of the investigator, would prevent completion of study participation or interfere with the analysis of the study results, such as history of non-compliance or unreliability

Outcomes

Primary Outcomes

Changes in radiographic bone fill

Changes in radiographic bone fill measured from the implant shoulder to the first bone to implant contact with ImageJ software, in parallelized periapical x-rays with individual silicone bite blocks

Time frame: Baseline, 3 months, 6 months and 12 months post-surgery

Secondary Outcomes

Changes in pocket probing depth

Depth of the peri-implant sulcus/pocket measured in millimeters with a 15-UNC (University of North Carolina) periodontal probe, at six sites per implant without the crown

Time frame: At baseline, after non-surgical therapy, 6 months and 12 months post-surgery

Changes in bone probing depth

Distance from the mucosal margin to the peri-implant bone measured in millimeters with a 15-UNC (University of North Carolina) periodontal probe under local anesthesia, at six sites per implant without the crown

Time frame: At baseline, after non-surgical therapy and 12 months post-surgery

Changes in modified plaque index

Presence or absence of plaque assessed at six sites per tooth/implant in the whole mouth, excluding third molars

Time frame: At baseline, after non-surgical therapy, 6 months and 12 months post-surgery

Changes in full mouth bleeding scores

Presence or absence of bleeding after probing with a 15-UNC (University of North Carolina) periodontal probe, assessed at six sites per tooth/implant in the whole mouth, excluding third molars. The presence of bleeding in each site will be scored 1, and the absence of bleeding will be scored 0. Full mouth bleeding score will be expressed in percentage and calculated as follows: number of sites bleeding / number of sites explored \^ 100

Time frame: At baseline, after non-surgical therapy, 6 months and 12 months post-surgery

Soft tissue healing scores

Extent of soft tissue healing after surgery following Landry et al. Healing Index (1988): * Healing index 1 - Very Poor * Healing index 2 - Poor * Healing index 3 - Good * Healing index 4 - Very good * Healing index 5 - Excellent

Time frame: 1 week, 2 weeks and 4 weeks post-surgery

Pain assessment

Participants´ subjective pain assessed using a Visual Analogue Scale (VAS) with ratings from 0-10, whereof 0 = no pain and 10 = very intense.

Time frame: 1 week, 2 weeks and 4 weeks post-surgery

Oral Health Impact Profile (OHIP-14)

Self-reported dysfunction, discomfort and disability attributed to the participants´ oral condition

Time frame: Baseline, 3 months, 6 months and 12 months post-surgery

Adverse events´ occurrence

Occurrence of any untoward, undesired or unplanned event in the form of signs, symptoms, disease, or laboratory or physiologic observations occurring in a subject participant in the clinical investigation. The event does not nee to be casually related to the cliinical investigation

Time frame: Up to 12 months post-surgery

Guided Bone Regeneration of Peri-implant Defects Comparing Submerged Versus Non-submerged Healing

Overview

Conditions

Interventions

Eligibility

Locations (1)

Outcomes

Primary Outcomes

Secondary Outcomes

Central Contacts