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Clinical Trials/CTRI/2025/02/080500
CTRI/2025/02/080500Not yet recruitingPhase 4

Comparison Between Use of Platelet-Rich Fibrin Membrane and Collagen Membrane Using Guided Tissue Regeneration Technique for Management of Infrabony Defects: A Clinical and Radiographic Study.

Dr Arti Odedara1 site in 1 country20 target enrollmentStarted: March 1, 2025Last updated:
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Trial Snapshot

Phase
Phase 4
Status
Not yet recruiting
Sponsor
Enrollment
20
Locations
1
Primary Endpoint
To gain vertical bone fill
Study OverviewStudy DesignEligibility CriteriaOutcomesInvestigatorsSitesRecords & IdentifiersSimilar Trials

Study Overview

Brief Summary

The
data will be collected from the patients will be selected visiting the OPD of the
Department of Periodontology, Government Dental College and Hospital,
Jamnagar, Gujarat. After informing the patient about the study and completing
the formalities in the consent form, the patients will be enrolled and data
collection in the proforma will be done.
Written informed consent
will be obtained from all study participants before starting of the study.

The participants will be  randomly allocated with envelope method into the following groups:

Group A : Open flap debridement with placement of  platelet rich fibrin membrane

Group B : Open flap debridement with placement of collagen membrane

Study Design

Study Type
Interventional
Allocation
Coin toss, Lottery, toss of dice, shuffling cards etc
Masking
None

Eligibility Criteria

Ages
18.00 Year(s) to 60.00 Year(s) (—)
Sex
All

Inclusion Criteria

  • •a) Probing pocket depth was more than 5mm following initial therapy.
  • •b) Age 18- 60 years c) Interproximal angular infrabony defects more than 3mm.
  • •d) Acceptable oral hygiene before access flap surgery.

Exclusion Criteria

  • •a) Any systemic disease which would alter the clinical outcome.
  • •b) Habit of tobacco in any form.
  • •c) Have no history of a previous periodontal surgery on a specified site for the last 6 months.

Outcomes

Primary Outcomes

To gain vertical bone fill

Time Frame: Baseline, 4 weeks, 12 weeks

Secondary Outcomes

  • Better wound healing(Baseline, 4 weeks, 12 weeks, 24 weeks)

Investigators

Sponsor
Dr Arti Odedara
Sponsor Class
Government medical college
Responsible Party
Principal Investigator
Principal Investigator

Dr. Arti Odedara

Department of Periodontology and Implantology

Study Sites (1)

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