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Clinical Trials/NCT04877145
NCT04877145CompletedNot Applicable

Single Drill Vrs Sequential Drill Dental Implants Placement

Assiut University2 sites in 1 country61 target enrollmentStarted: February 12, 2017Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
61
Locations
2
Primary Endpoint
osseointegration of the dental implants

Study Overview

Brief Summary

dental implants are usually placed by sequential set of drills which could increase the time of the surgery and could raise the temperature of the osteotomy preparation so a new drill was designed to place the implants fast and easy way

Detailed Description

Dental implant success is evident nowadays with the predictable functional and aesthetic results obtained . Simplified techniques and approaches are preferred for the convenience of both the patients and operators . Current research is focusing on decreasing the number of instruments used, shortening of the operation time and performing flapless approaches for implant placement whenever possible. This is done to reduce the postoperative complaints, such as pain, swelling and bleeding; thus decreasing the need for analgesics and minimising the occurrence of morbidity .

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

Eligibility Criteria

Ages
18 Years to 60 Years (Adult)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • The inclusion criteria :
  • implant recipient sites free from any pathological conditions.
  • Patients who were cooperative, motivated and hygiene conscious were selected.
  • non smoker patients
  • exclusion criteria :
  • Patients unable to undergo minor oral surgical procedures
  • patients with a history of drug abuse or catabolic drugs were not included.
  • Patients with a history of psychiatric disorder and those with unrealistic expectations about the aesthetic outcome of implant therapy were also excluded.
  • Patients with insufficient vertical inter-arch space, on centric occlusion, to accommodate the available restorative components .
  • Uncontrolled diabetic patients
  • Patient who had any systemic condition that may contraindicate implant therapy (impaired wound healing - bleeding disorders
  • patients who had any habits that might jeopardise the osseointegration process, such as heavy smoking and alcoholism.
  • Patients with para-functional habits that produce overload on the implant, such as bruxism and clenching were excluded.

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

osseointegration of the dental implants

Time Frame: 6 months

healing and union of the dental implants with the surrounding bone measured by torque wrench exceeds 30 N/CM

Secondary Outcomes

  • bone loss(6 months , 1 ,2 and 3 years after function)
  • mobility(6 months)

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Ahmed Mortada

lecturer of periodontology and oral implantology - faculty of dentistry , Assiut University - Egypt

Cairo University

Study Sites (2)

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