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Guided Bone Regeneration With Particulate Versus Block Graft

T

TC Erciyes University

Status

Completed

Conditions

Surgery

Study type

Observational

Funder types

Other

Identifiers

Details and patient eligibility

About

The aim of present study was to compare two bone augmentation techniques (Guided Bone Regeneration, GBR, with autogenous block graft and GBR with particulate autograft plus xenograft) in terms of efficacy, complications, operational parameters (cost of the materials used, time for patient preparation, time for surgery, fatigue of the physician caused by surgery) tolerability by the patient and patient comfort.

Full description

The aim of present study was to compare two bone augmentation techniques (Guided Bone Regeneration, GBR, with autogenous block graft and GBR with particulate autograft plus xenograft) in terms of efficacy, complications, operational parameters (cost of the materials used, time for patient preparation, time for surgery, fatigue of the physician caused by surgery) tolerability by the patient and patient comfort. 30 systemically healthy individuals with inadequate alveolar bone crest width who requested implant placement (15 Female and 15 Male) participated in this study. After an initial examination, 15 patients were assigned to GBR with block graft (GBR-BG) and 15 were assigned to GBR particulate autograft plus xenograft (GBR-AX). Bone thickness was recorded before surgery and at a post-operative 6th month. Complications as Bleeding, Hematoma, Flap dehiscence, Infection, Numbness were evaluated. Patients were requested to record pain and swelling via visual analog scale (VAS) at 3rd, 7th and 14th days after surgery. The swelling was also recorded by an experienced clinician at 3rd, 7th and 14th days after surgery. Cost, time for patient preparation, time for surgery, fatigue of the physician caused by surgery were also determined.

Enrollment

30 patients

Sex

All

Ages

30 to 62 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • 30 to 62 years of age
  • systemically health
  • no smoking
  • no use of medications for previous 6 months
  • no pregnancy and lactation
  • no contraindications for periodontal surgery.

Exclusion criteria

  • <30 and >62 years of age
  • patients with systemic disease
  • smoking habit ( current or past)
  • any medication
  • acute illness
  • pregnancy or lactation

Trial design

30 participants in 2 patient groups

Guided Bone Regeneration with Particulate graft
Description:
patients who had inadequate alveolar crest (crest width <4mm) and requested of dental implant placement, treated with guided bone regeration with particulate graft
Guided Bone Regeneration with block graft
Description:
patients who had inadequate alveolar crest (crest width <4mm) and requested of dental implant placement, treated with guided bone regeration with block graft

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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