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Treatment of loss of gums using material obtained from animals or material obtained from patients own blood

Recruiting
Conditions
Gingival recession,
Registration Number
CTRI/2023/12/060865
Lead Sponsor
Polimera Sanathana
Brief Summary

Gingival recession is defined as the apical displacement of gingival margin to the cementoenamel junction exposing the root surfaces which may lead to dentinal hypersensitivity, root caries and aesthetic concerns to patients. Connective tissue graft along with coronally advanced flap is considered as the gold standard treatment protocol in the management of gingival recession. However , due to drawbacks of connective tissue grafts like palatal morbidity as a result of secondary surgical site and patient’s fear of pain the proposed study aims to compare the clinical efficacy of volume stable xenogenic collagen matrix incorporated with injectable platelet rich fibrin versus platelet rich fibrin obtained by horizontal spin protocol in the treatment of gingival recession defects. If both the groups shows similar significant results, in future we may recommend the groups protocol as a choice of treatment in the management of gingival recession defects.

Detailed Description

Not available

Recruitment & Eligibility

Status
Open to Recruitment
Sex
All
Target Recruitment
52
Inclusion Criteria
  • 1.Cairo’s RT1 & RT2 class of recession defects in maxillary anteriors and premolars.
  • 2.Sites with minimum depth of recession greater then or equal to 2mm.
  • 3.Isolated or multiple adjoining recession involving less than or equal to 3 teeth.
Exclusion Criteria
  • 1.Sites with probing pocket depth greater than 4mm.
  • 2.Teeth with mobility and/or associated with trauma from occlusion.
  • 3.Sites with dental caries and prosthetic restorations.
  • 4.Patients who exhibit unacceptable oral hygiene compliance during/or after phase one periodontal therapy.
  • 6.Pregnant and lactating women.
  • 8.Patients with known platelet disorders or using any medication that are known to interfere with platelet function.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
2.To assess and compare the percentage of Complete root coverage achieved at 6months between the treatment groups.Baseline and 6months
1.To assess & compare the changes in the recession height from baseline to 6 months, within & between the treatment groups.Baseline and 6months
Secondary Outcome Measures
NameTimeMethod
1.To assess & compare the changes in the Gingival thickness from baseline to 6 months, within & between the treatment groups.Baseline and 6months

Trial Locations

Locations (1)

SRM Dental college and Hospital

🇮🇳

Chennai, TAMIL NADU, India

SRM Dental college and Hospital
🇮🇳Chennai, TAMIL NADU, India
DrAnupama Tadepalli
Principal investigator
9677065517
anupamamds@gmail.com

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