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Clinical Trial Details — Status: Enrolling by invitation

Administrative data

NCT number NCT04195841
Other study ID # 02_D012_91553
Secondary ID
Status Enrolling by invitation
Phase N/A
First received
Last updated
Start date November 20, 2018
Est. completion date January 1, 2021

Study information

Verified date January 2021
Source Krishnadevaraya College of Dental Sciences & Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The present study is a human, prospective, parallel, randomised controlled clinical trial conducted to check the interproximal bone loss of Z shaped incision over conventional sulcular H shaped incision.The trial is in accordance with the Consolidated Standards of Reporting Trials (CONSORT) criteria, 2010.


Description:

Twenty healthy individuals satisfying the inclusion and exclusion criteria were recruited for the study. A detailed, thorough medical and dental history was obtained and each patient was subjected to comprehensive clinical and radiological examination. All patients were informed about the nature of the study, the surgical procedure involved, potential benefits and risks associated with the surgical procedure and written informed consent were obtained from all patients. In the test group patients Z shaped incision was done to place implants and H shaped sulcular incision was placed in control group. The clinical and radiographic parameters were recorded at baseline,24 hours,7days, three months and six months postoperatively.


Recruitment information / eligibility

Status Enrolling by invitation
Enrollment 20
Est. completion date January 1, 2021
Est. primary completion date December 31, 2020
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group N/A and older
Eligibility Inclusion Criteria: 1. Patients with single or multiple edentulous spaces in the maxillary and mandibular arches having Siebert's Class 1 and 2 ridge defects. 2. Patients willing to participate in the study. 3. Patients above 18 years of age. 4. Patients exhibiting keratinized tissue width more than or equal to 2 mm. 5. Systemically healthy patients. 6. Patients who demonstrate full mouth plaque control and bleeding scores<25% and showing good compliance. Exclusion Criteria: 1. Patients who do not give consent. 2. Untreated periodontal disease, caries. 3. Insufficient oral hygiene. 4. Smokers. 5. Previous radiation therapy. 6. Patients with known systemic diseases and conditions 7. Pregnant and lactating women.

Study Design


Intervention

Procedure:
Z shaped incision
After local anaesthesia, a mucoperiosteal flap will be elevated at the edentulous ridge with two horizontal incisions placed with a no MB 69 blade, 1-2 mm away from the papilla of the teeth adjacent to the edentulous space following the mesial and distal contour of the teeth. The extend of the incisions should be up to the proximal line angles of the adjacent teeth. These two horizontal incisions are then connected by an oblique incision from the disto-buccal to mesio lingual point angles. A periosteal elevator is used to elevate a full thickness mucoperiosteal flap buccally and lingually to the level of the mucogingival junction, exposing the alveolar ridge of the implant surgical sites. Endosseous implant placement is done followed by simple interrupted resorbable sutures
H shaped incision
After local anaesthesia, a mucoperiosteal flap is elelevated by placing sulcular incisions placed in the proximal sides of the adjacent tooth facing the edentulous space in a bucco lingual direction extending between the proximal line angles using a MB 69 blade. Mid crestal incision performed in the attached mucosa of the edentulous area connecting the sulcular incisions of the adjacent teeth from the distal to mesial tooth. A full thickness mucoperiosteal flap will be elevated buccally and lingually to the level of the mucogingival junction to expose the alveolar ridge of the implant surgical sites using a periosteal elevator. Endosseous implant will be placed, followed by simple interrupted resorbable sutures.

Locations

Country Name City State
India Krishnadevaraya college of dental sciences Bangalore Karnataka

Sponsors (1)

Lead Sponsor Collaborator
Krishnadevaraya College of Dental Sciences & Hospital

Country where clinical trial is conducted

India, 

Outcome

Type Measure Description Time frame Safety issue
Primary Inter proximal bone level Mesial and distal peri-implant radiographic bone level will be recorded in millimetres on the digital radiographs with grid at baseline and follow up 6 months
Primary Healing Early wound healing index is assessed. values 1-5 is present. Increase in score depicts worse healing. 7 days
Secondary Visual Analouge Score a questionnaire will be given to the patients in which their responses for Visual Analog Score that ranges from 1-10 values and highest values indicate the worst outcome, variation in feeding habits, analgesics dosage is recorded. 7 days
Secondary Clinical attachment level The amount of attached gingiva was measured by subtracting the probing depth from the amount of keratinised mucosa 3 months
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