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Clinical Trials/CTRI/2013/01/003286
CTRI/2013/01/003286
Completed
未知

CLINICAL AND RADIOGRAPHIC ASSESSMENT OF BONE REGENERATION USING ALENDRONATE SODIUM GEL AS ANADJUNCT TO SURGICAL THERAPY FOR THE TREATMENT OF OSSEOUS DEFECTS IN CHRONIC PERIODONTITIS- A COMPARATIVE STUDY

PRINCIPAL INVESTIGATOR0 sites30 target enrollmentTBD

Overview

Phase
未知
Intervention
Not specified
Conditions
Not specified
Sponsor
PRINCIPAL INVESTIGATOR
Enrollment
30
Status
Completed
Last Updated
4 years ago

Overview

Brief Summary

No summary available.

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

Investigators

Eligibility Criteria

Inclusion Criteria

  • a)Patient of either sex within the age group of 35\-50 years.
  • b)Systemically healthy patients.
  • c)Clinical diagnosis of moderate generalized chronic periodontitis.
  • d)Patients with probing depth \>\=5 mm or clinical attachment loss \> 4 to 6 mm bilaterally as evidenced by clinical examination.
  • e)Patients with vertical bone loss \> 5mm as evidenced on IOPA radiograph.
  • f)Patients with acceptable oral hygiene following Phase\-I therapy.

Exclusion Criteria

  • a)Patients with presence of systemic conditions or disease affecting bone density e.g. Osteoporosis, Pagetâ??s disease.
  • b)Patients with known or suspected allergy to Alendronate/ bisphosphonates group.
  • c)Patients with Aggressive Periodontitis.
  • d)Patients with horizontal bone loss.
  • e)Patients without any contradictions for periodontal surgery.
  • f)Patients with a history of drug intake that can affect bone metabolism in the past 6 months. E.g. NSAIDs.
  • g)Patients who are current smokers, or ex smokers for less than five years.
  • h)Pregnant or lactating females.
  • i)Patients who are alcoholics.
  • j)Immunocompromised patients.

Outcomes

Primary Outcomes

Not specified

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