Peri-implant Papillary Height Comparison in Microsurgically and Macrosurgically Placed Dental Implants
NCT ID: NCT04189328
Last Updated: 2019-12-10
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
20 participants
INTERVENTIONAL
2017-12-10
2019-09-30
Brief Summary
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Detailed Description
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32 participants, 16 in two groups were assigned randomly. Microsurgical approach using microsurgical instruments and magnifying loupes were used for one group participants and similar procedure without magnifying loupes and microsurgical instruments was done in the other group.
comparsion of the microsurgical outcome is done by measuring peri implant papilla gain and radiographic crestal bone loss will be done between the groups.
Conditions
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
DOUBLE
Study Groups
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control group
conventional macrosurgical implant placement
macrosurgical dental implant placement
macrosurgical placement of single dental implants
test group
microsurgical implant placement
dental implant placement using magnifying loupes and microsurgical instruments
microsurgical dental implant placement employin splt finger technique by Misch
Interventions
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dental implant placement using magnifying loupes and microsurgical instruments
microsurgical dental implant placement employin splt finger technique by Misch
macrosurgical dental implant placement
macrosurgical placement of single dental implants
Eligibility Criteria
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Inclusion Criteria
* Non smokers
* Patients who do not report any relevant medically comprimising conditions or had not received any radiation therapy in head and neck region for cancer therapy.
* Subjects with satisfactory residual ridges who demonstrated adequate bucco-lingual and mesio-distal space for implant placement, that facilitates primary stability.
* Patients who demonstrate Plaque Index \<10% and good compliance.
* Full mouth bleeding scores ≤25% before the implant placement.
* Sites with sufficient band of keratinised mucosa.
Exclusion Criteria
* Patients on anticancer therapy and immunosuppressant drugs.
* Implants to be placed in sites with previous periodontal disease
* Bleeding disorder or on anticoagulant therapy
* Systemic diseases that would negatively influence wound healing
18 Years
ALL
Yes
Sponsors
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Krishnadevaraya College of Dental Sciences & Hospital
OTHER
Responsible Party
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Principal Investigators
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Dr.Joann pauline George, MDS
Role: PRINCIPAL_INVESTIGATOR
Krishnadevaraya college of dental sciences
Locations
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Krishnadevaraya college of dental sciences and hospital
Bangalore, Karnataka, India
Countries
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Other Identifiers
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02_D012_82168
Identifier Type: -
Identifier Source: org_study_id