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

Single Drill Vrs Sequential Drill Dental Implants Placement

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04877145
Enrollment
61
Registered
2021-05-07
Start date
2017-02-12
Completion date
2021-04-20
Last updated
2021-05-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Implant Complication

Keywords

implants

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 .

Interventions

OTHERdrill

single 3.25 mm stainless steel drill

Sponsors

Assiut University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 60 Years
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.

Design outcomes

Primary

MeasureTime frameDescription
osseointegration of the dental implants6 monthshealing and union of the dental implants with the surrounding bone measured by torque wrench exceeds 30 N/CM

Secondary

MeasureTime frameDescription
mobility6 monthsthe fixation of the implants checked by perio test M (-8- 0) INDICATES nonmobile
bone loss6 months , 1 ,2 and 3 years after functionby periapical xray the bone loss measured from the platform of the implant if present unit of measurement : mm

Countries

Egypt

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026