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Implant Placement Using a Newly Designed Single Drill Versus Conventional Sequential Drills

A

Assiut University

Status

Completed

Conditions

Implant Complication

Treatments

Other: drill

Study type

Interventional

Funder types

Other

Identifiers

NCT04877145
17300587

Details and patient eligibility

About

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

Full 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 .

Enrollment

61 patients

Sex

All

Ages

18 to 60 years old

Volunteers

Accepts Healthy Volunteers

Inclusion and exclusion criteria

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.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Quadruple Blind

61 participants in 2 patient groups

single drill
Experimental group
Description:
one drill to place the implants 3.25mm diameter stainless steel drill was used.
Treatment:
Other: drill
sequential drills
Active Comparator group
Description:
For the control group, four drills (2.2mm, 2.75mm, 3.25mm and 4mm diameter),
Treatment:
Other: drill

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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