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Treatment Of Gum Disease Using Blood units And Tissue derivatives

Not Applicable
Completed
Conditions
screeing intervention
Registration Number
CTRI/2018/10/016189
Lead Sponsor
Angelin Rejoice
Brief Summary

The study is an randomized clinical trial, aimed to find the efficacy of platelet rich fibrin matrix and collagen membrane on miller’s class I and class II gingival recession. 20 identical bilateral recession defects will be selected and randomly allocated in to Group A ( collagen membrane) and Group B ( PRFM). The procedure will be explained to the patient and  informed consent is obtained. In the presurgical phase, scaling and re-evaluation carried on follwed by coronally advanced flap and placement of membrane or PRFM  according to the desired site,  followed by placement of periodontal dressing. Post-operative instructions are given, along with prescription of antibiotics, analgesics and chlorhexidine mouth wash. The study duration of two years, the clinical parameters will be recorded at baseline, 3 months and 6 months.

Detailed Description

Not available

Recruitment & Eligibility

Status
Completed
Sex
All
Target Recruitment
20
Inclusion Criteria
  • 1 Systemically healthy subjects.
  • 2 Age: 18-50 years.
  • 3 Identical bilateral Miller’s class I and II isolated gingival recession.
  • 4 Patients with more than 1mm of width of keratinized gingiva.
  • •Presence of good oral hygiene maintenance.
Exclusion Criteria
  • 1 History of subjects who underwent previous periodontal surgery for past 6 month.
  • 2 Presence of dehiscence or fenestration.
  • 3 Malposed / rotated teeth/ root caries.
  • 4 Smokers and chewers of tobacco.
  • 5 Pregnant or lactating mother.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
•Recession width at cemento-enamel junction.baseline, 3months, 6 months
•Clinical attachment level.baseline, 3months, 6 months
•Probing depth.baseline, 3months, 6 months
•Recession depthbaseline, 3months, 6 months
•Keratinized gingival width.baseline, 3months, 6 months
Secondary Outcome Measures
NameTimeMethod
Gingival index, Plaque indexBaseline, 3months, 6 months
. Assessment of soft tissue healing. 1 week, 3 months, 6 months

Trial Locations

Locations (1)

The oxford dental college

🇮🇳

Bangalore, KARNATAKA, India

The oxford dental college
🇮🇳Bangalore, KARNATAKA, India
Angelin Rejoice
Principal investigator
9620977991
angelinrejoicejohn@gmail.com

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