RESEARCH
QUESTION-
Which amongst the
Densah bur and Osteotome for maxillary sinus lift with simultaneous Implant
placement is more effective in implant stability and operation time ?
RESEARCH
HYPOTHESIS-
Null hypothesis- :
There is no significant difference between using the Densah burs or the
osteotome for transcrestal maxillary sinus lifting with simultaneous implant
placement regarding implant stability
and operation time.
Alternative hypothesis-
There will be difference between surgical outcomes of using the Densah burs or
the osteotome for transcrestal maxillary sinus lifting with simultaneous
implant placememnt regarding implant
stability and operation time.
AIM OF THE
STUDY:
To compare the treatment
outcomes of Densah Burs and
Osteotomes for maxillary sinus lift with simultaneous Implant
placement in Posterior Maxilla.
OBJECTIVES
1. To Evaluate the Primary and Secondary Stability
of Dental implant after placement by Densah
Bur and Osteotome.
2. To Evaluate the crestal bone loss of Dental
Implant by Densah bur and Osteotome.
3. To Evaluate the Time taken for implant
placement by Densah Bur and Osteotome.
4. To Evaluate the post operative pain by
Densah Bur and Osteotome.
5. To Evaluate the post operative complication
by Densah Bur and Osteotome.
MATERIALS AND
METHODS:
The present study will
be conducted in the Department Of Periodontology, Rural Dental Hospital, Loni. A total
of 15 patients, sample size 30 with missing maxillary premolars or molars and with limited
vertical bone height below the maxillary sinus floor (6mm or more) received
implants either with osteotome or with osseodensification densah bur transcrestal sinus
lifting.
STUDY DESIGN:
Study Type :
Experimental (Phase 3)
Study Design :
Randomized controlled clinical trial
Period of Study : 2
years
Study Start Date :
March 2025 (after the IEC approval)
Setting : Department of
Periodontology, Rural Dental Hospital, Loni.
INCLUSION
CRITERIA
· All the patients giving informed consent will
be included in the study.
· Patient with Age group 18-60 years of either
sex.
· Posterior missing teeth and tooth .(Kennedys
classification 1,2,3,6)
· Patient with no history of sinus surgery.
· Patient with minimal height of 6mm in
edentulous area.
· All types of bone density (D1-D4) based on
CBCT.
· Patients who accepted to come for follow up .
EXCLUSION
CRITERIA
· Patients undergoing and with history of radiotheraphy.
· Medically compromised patients.
· Patient on long term steroid therapy
· Heavy smokers(more than 20 cigarettes )
· Restricted mouth opening .
METHODOLOGY:
All patients satisfying
the above inclusion and exclusion criteria will be given a unique code and subjected to a
well-defined random allocation method.
Randomization
technique: Each eligible patient indicated to undergo the trial will be subjected to random
lottery method.
A box will be made containing
15 slips with equal number of right and left sides. Each patient will be asked
to pick up a lottery slip from the box. The side picked up by the patient will
be taken as Test group-1. This will be done to support randomization.
1. Test group Densah
bur Technique
2. Control group OsteotomeTechnique
After selecting the
slip, dental implant will be placed accordingly.
STUDY CONDUCT
All the patients
satisfying the above inclusion and exclusion criteria will be grouped into :
Group A: The patients
being treated by Densah bur technique with simultaneous implant placement.
Group B: The patients
being treated by Osteotome technique with simultaneous implant placement.
VARIABLES
|
Sr
No
|
Measurement
of Variable
|
Measurement
scale
|
Method
of Measurement
|
|
1
|
Age
|
Ratio
scale
|
Interview/
Records
|
|
2
|
Gender
|
Nominal
scale
|
Observations
|
|
3
|
Primary
Stability of Dental Implant
|
Oridinal
scale
|
Periotest
|
|
4
|
Secondary
Stability of Dental Implant
|
Ordinal
Scale
|
Periotest
|
|
5
|
Crestal
Bone Loss
|
Ratio
Scale
|
CBCT
|
|
6
|
Time
taken for Implant placement
|
Ratio
Scale
|
Interview
|
|
7
|
Post
operative Pain
|
Ordinal
Scale
|
VAS
|
|
8
|
Post
operative Complications
|
Ordinal
Scale
|
Clinical evaluation and
radiographic diagnosis
|
|
Sr
No
|
Measurement
Variable
|
Assessment
|
|
1
|
Stability
of Dental Implant
|
Periotest
-8 to 0 =good
osteointegration
+1 to +9 = Needs
clincal examination
+10 to +50 = Osteointegration
insufficient
|
|
2
|
Crestal
Bone Loss
|
CBCT
pre operatively
CBCT
after 3 months
|
|
3
|
Time
taken for Implant placement
|
Stopwatch
From
first drill to placement of dental implant
|
|
4
|
Post
operative Pain
|
Visual
Analogue Scale (VAS)
|
INITIAL THERAPY:
The information about
the need of study will be clarified and a signed informed consent will be taken from
patients. Study protocol will be approved by the Institutional Ethical Committee of PIMS (DU)
Loni.
In the first visit,
full mouth scaling will be undertaken followed by root planing . Plaque control measures will
be given to the patient.
TREATMENT
PROCEDURE:
·
The implant placement was done by using surgical motor. Before the Implant
Osteotomy Procedure started, local anaesthesia containing lignocaine with
adrenaline (1:80,000) was injected.The incision was carried out with 15 no
blade and mucoperiosteal flap was reflected by giving crestal incision.
·
The process of implant osteotomy was started with the pilot drill to accurately
reproduce the angulation. A series of drills were used to prepare the osteotomy
site precisely and incrementally for an implant. A surgical guide or stent is
inserted, checked for proper positioning, and used throughout the procedure to
direct the proper implant placement.
·
This was followed by using Implant Osteotome and sequential ostetome was done
as per required size with the help of mallet and ostetome instrument ,insertion
was done .It is important to create a recipient site that is very accurate in
size an angulation. It was screwed in and tightened using the implant ratchet
provided in the surgical kit. It was made sure that a minimum torque was
obtained while screwing in the implant, implant stability was achieved.
· Osseodensification
surgical drilling protocol, implant beds will be prepared using specially
designed drills (Densah™ burs) that helps to densify bone, as they prepare an
osteotomy. Densah burs are specially designed burs that has many lands with a
large negative rake angle which works as non-cutting edges to create a layer of
compact, dense bone surrounding the wall of the osteotomy. They are marked with
laser markings from 8-20 mm depth. Densah burs are designed to have a cutting
chisel edge and a tapered shank so as they enter deeper in to the osteotomy,
they have a progressively increasing diameter that controls the expansion
process. Densah Burs can be used in both Cutting(Clockwise) and Densifying
(Anticlockwise) modes within the same procedure. Densah burs are externally
irrigated and designed to be used at drill speeds of 800-1500 rpm.
· OD does not excavate bone
but simultaneously compacts and autografts the particulate bone thereby
preserving vital bone tissue. This is achieved using specialized densifying
burs. When these specialized drills are used at high speed in an anticlockwise
direction (Densifying mode) with steady external irrigation, the dense compact
bone tissue is created along the osteotomy walls. The pumping motion (in and
out movement) creates a rate dependent stress to produce a rate dependent
strain and allows saline solution to gently pressurize the bone walls.
· Once the implants were inserted, primary
implant stability were evaluated by Periotest and the cover screws secured, the
surgical sites were thoroughly irrigated with sterile saline to remove debris
and clean the wound.
· The time for implant
placement was started from the 1st drill (pilot) to implant placement using
Digital stop-watch .
· Proper closure of the
flap over the implants is essential. Post-surgical intraoral OPG was taken to
assess the implant position.
· Standard Post-surgical
instructions were delivered and instructions regarding home care and
medications were given.
STUDY PERIOD:
24 months starting from
the time of approval of the study.
ETHICAL
APPROVAL:
It will be made clear
with the potential subjects that participation will be voluntary and written informed
consent will be obtained from those who agree to participate.
STATISTICAL
ANALYSIS:
All the data will be
analyzed by applying appropriate tests of significance.
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