Peri-implant Papillary Height Comparison in Microsurgically and Macrosurgically Placed Dental Implants

Overview

This study compares the peri-implant soft tissue and crestal bone loss around single implants when placed macrosurgically and microsurgically.

Full Title of Study: “Clinical and Radiological Comparison of Peri Implant Soft Tissue Parameters and Crestal Bone Loss Around Microsurgically and Macrosurgically Placed Implants: A Randomised Controlled Clinical Trail”

Study Type

  • Study Type: Interventional
  • Study Design
    • Allocation: Randomized
    • Intervention Model: Parallel Assignment
    • Primary Purpose: Treatment
    • Masking: Double (Investigator, Outcomes Assessor)
  • Study Primary Completion Date: September 30, 2019

Detailed Description

Black triangles in dentition especially in the anterior teeth would pose an esthetic concern. Interdental papilla height is crucial for eliminating this black triangle.

32 participants, 16 in two groups were assigned randomly. Microsurgical approach using microsurgical instruments and magnifying loupes were used for one group participants and similar procedure without magnifying loupes and microsurgical instruments was done in the other group.

comparsion of the microsurgical outcome is done by measuring peri implant papilla gain and radiographic crestal bone loss will be done between the groups.

Interventions

  • Procedure: dental implant placement using magnifying loupes and microsurgical instruments
    • microsurgical dental implant placement employin splt finger technique by Misch
  • Procedure: macrosurgical dental implant placement
    • macrosurgical placement of single dental implants

Arms, Groups and Cohorts

  • Active Comparator: control group
    • conventional macrosurgical implant placement
  • Experimental: test group
    • microsurgical implant placement

Clinical Trial Outcome Measures

Primary Measures

  • peri-implant papilla height
    • Time Frame: 1 year
    • mesial and distal peri implant papilla height is measured in millimeter
  • marginal gingiva
    • Time Frame: 1 year
    • buccal marginal gingival height is measured
  • jemt papilla index
    • Time Frame: 1 year
    • papillary height gained around implant is scored using jemt papilla index 0 = no papilla and no indication of a curvature of the soft tissue adjacent to the implant crown are present; = less than one-half of the papilla height is present, and a convex curvature of the soft tissue adjacent to the implant crown and adjacent tooth can be observed; = at least one-half of the papilla height is present but not to the contact point between the teeth, the papilla is not completely harmonious with the adjacent papillae between the permanent teeth, and soft tissue is harmonious with adjacent teeth; = the papilla fills the entire proximal space and is harmonious with the adjacent papillae, and soft-tissue contour is optimal; = the papillae are hyperplastic and cover too much of the implant or the adjacent tooth, and the soft-tissue contour is irregular
  • crestal bone loss
    • Time Frame: 1 year
    • radiographic crestal bone level around the implants measured from 1st thread of the implant to the coronal or apical most bone level in millimeters.
  • pink esthetic score
    • Time Frame: 1 year
    • scoring assigned to 7 soft tissue criteria by an examiner as 0,1,2,3 and the average of the total score is considered the final score. a maximum score of 14 can be alloted

Secondary Measures

  • surgical time taken
    • Time Frame: 1 day
    • the time taken right from the incision to the implant placement is watched and recorded.
  • visual analogue scale score
    • Time Frame: 1 year
    • aesthetic score by the outcome investigator using VAS score sheet of 10 points. 1 being most painful and 10 being painless
  • probing depth
    • Time Frame: 1 year
    • peri implant probing depth at each follow up was recorded
  • plaque index
    • Time Frame: 1 year
    • plaque scores were recorded at each follow up 0.-0.9 good 1.0-1.9-fair 2-3-poor
  • gingival index
    • Time Frame: 1 year
    • gingival index scores were recorded at each followup 0.1-1-mild gingivitis 1.1-2- moderate gingivitis 2.1-3 severe gingivitis

Participating in This Clinical Trial

Inclusion Criteria

  • Patients desiring implant placement for replacement of missing tooth and willing to participate in the study
  • Non smokers
  • Patients who do not report any relevant medically comprimising conditions or had not received any radiation therapy in head and neck region for cancer therapy.
  • Subjects with satisfactory residual ridges who demonstrated adequate bucco-lingual and mesio-distal space for implant placement, that facilitates primary stability.
  • Patients who demonstrate Plaque Index <10% and good compliance.
  • Full mouth bleeding scores ≤25% before the implant placement.
  • Sites with sufficient band of keratinised mucosa.

Exclusion Criteria

  • • Pregnant and lactating females
  • Patients on anticancer therapy and immunosuppressant drugs.
  • Implants to be placed in sites with previous periodontal disease
  • Bleeding disorder or on anticoagulant therapy
  • Systemic diseases that would negatively influence wound healing

Gender Eligibility: All

Minimum Age: 18 Years

Maximum Age: N/A

Are Healthy Volunteers Accepted: Accepts Healthy Volunteers

Investigator Details

  • Lead Sponsor
    • Krishnadevaraya College of Dental Sciences & Hospital
  • Provider of Information About this Clinical Study
    • Sponsor
  • Overall Official(s)
    • Dr.Joann pauline George, MDS, Principal Investigator, Krishnadevaraya college of dental sciences

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