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Clinical Trials/CTRI/2020/03/024075
CTRI/2020/03/024075
Not yet recruiting
未知

Comparative evaluation of clinical and radiological parameters following the use of biphasic alloplastic material with Amniotic membrane / Collagen membrane for the management of periodontal intra-bony defects - A prospective double blind randomized controlled clinical trial.

nivedhav0 sites20 target enrollmentTBD

Overview

Phase
未知
Intervention
Not specified
Conditions
Health Condition 1: K053- Chronic periodontitis
Sponsor
nivedhav
Enrollment
20
Status
Not yet recruiting
Last Updated
4 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
March 13, 2020
Last Updated
4 years ago
Study Type
Interventional

Investigators

Sponsor
nivedhav

Eligibility Criteria

Inclusion Criteria

  • 1 Age 21\-50 years
  • 2 Patients with moderate to severe localized periodontitis with a Probing Depth (PD) \>\=6 mm and an intrabony component of more than 3 mm as detected on Intra oral periapical radiographs (IOPAR) and bone sounding (Sali 2016\).
  • 3 Intrabony defect angle of less than 40 degree (Sali 2016\).
  • 4 Circumferential defect with interdental intrabony defect depth of more than 3mm will be included.
  • 5 Nonsmoker (Never smoker) or former smoker (Does not smoke now and has not smoked at all for a minimum of the last 12 consecutive months)

Exclusion Criteria

  • 1 Current Smokers (smokers who have smoked more than 100 cigarettes in their lifetime and currently smoke)
  • 2 Systemic chronic conditions known to be associated with periodontitis or with changes in systemic inflammation: Diabetes, Cardiovascular diseases, Rheumatoid Arthritis, Rheumatic Fever, SLE, Malignancy, Respiratory diseases, Renal diseases, Other (e.g., autoimmune diseases, fungal infections, immunological deficiencies, etc.)
  • 3 Pregnant / Lactating mothers
  • 4 Previous History of periodontal treatment at the selected site
  • 5 Teeth with intrabony defect component and furcation involvement were also excluded from the study.

Outcomes

Primary Outcomes

Not specified

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