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Influence of Z Shaped and Conventional Sulcular Incisions on Healing and Interproximal Bone Loss in Implant Surgery

K

Krishnadevaraya College of Dental Sciences & Hospital

Status

Unknown

Conditions

Healing Surgical Wounds
Bone Loss

Treatments

Procedure: Z shaped incision
Procedure: H shaped incision

Study type

Interventional

Funder types

Other

Identifiers

NCT04195841
02_D012_91553

Details and patient eligibility

About

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.

Full 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.

Enrollment

20 patients

Sex

Volunteers

Accepts Healthy Volunteers

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.

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

20 participants in 2 patient groups

Test group
Experimental group
Description:
Two horizontal incisions placed 1-2 mm away from the papilla of the teeth adjacent to the edentulous space following the mesial and distal contour of the teeth. These two horizontal incisions are then connected by an oblique incision from the disto-buccal to mesio lingual point angles.
Treatment:
Procedure: Z shaped incision
Control group
Experimental group
Description:
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 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
Treatment:
Procedure: H shaped incision

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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