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A Comparision Between Healing Of Dimentionally Altered Autograft With An Allograft For Treatment Of Gum Recessions

Not yet recruiting
Conditions
ISOLATED GINGIVAL RECESSIONS
Registration Number
CTRI/2020/02/023387
Lead Sponsor
ALLURI SRI NEHA RAJU
Brief Summary

AIM:To evaluate the efficacy of healing and pain perception after usingModified Connective tissue graft and Collagen membrane in isolated Millersclass I and class II Gingival Recessions.

OBJECTIVES OF THE STUDY:1. Evaluating the efficacy of Modified Connective Tissue Graft andCollagen Membrane in treating gingival recession.2. Evaluating the healing and pain perception with Modified ConnectiveTissue Graft and Collagen Membrane in treating Gingival Recession.3. Estimating the difference in clinical parameters i.e. Probing Depth,Clinical Attachment Level, Gingival Thickness, Keratinized TissueHeight between Modified Connective Tissue Graft and CollagenMembrane.

NEED FOR THE STUDY :

So far there is only one randomised control trail analysing the effect ofModified Connective Tissue Graft dimensions on the predictability of rootcoverage. Literature stated that Sub epithelial Connective Tissue Graft is goldstandard procedure although Guided Tissue Regeneration has also shownequal results in predictability of root coverage. This study is the first of its kind to compare and analyse the healing andpredictability of dimensionally altered Modified Connective Tissue Graft(MCTG) with Guided Tissue Regeneration.

Detailed Description

Not available

Recruitment & Eligibility

Status
Not Yet Recruiting
Sex
All
Target Recruitment
12
Inclusion Criteria
  • Patients with mean age group of 20-50yrs.
  • Patients having one Pair of isolated Gingival Recessions.
  • Patients with Millers class I or class II Buccal Gingival Recessions.
  • Patients who had defects in maxillary anteriors and premolars and who have ability to maintain good oral hygiene.
  • Patients willing to comply with all the study-related procedures, and those available for follow-up.
  • The plaque index following periodontal therapy has to be <1.
Exclusion Criteria
  • Patients who had history of prolonged use of antibiotics.
  • Patients who had periodontal therapy in the preceding 6 months.
  • Pregnant and lactating women.
  • Patients who use tobacco in any form.
  • Patients who had history of systemic diseases.
  • Patients Unwilling for treatment.
  • Gingival recession associated with severe cervical abrasion.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Complete Root Coverage With Faster Healing Without Post Operative PainEvery Day In The 1st Week | Once In 6th, 12th And 24th Week
Secondary Outcome Measures
NameTimeMethod
Stablility Of Root CoverageDiffrence In Healing Index And Pain Perception In The First Week

Trial Locations

Locations (1)

LENORA INSTITUTE OF DENTAL SCIENCES

🇮🇳

Godavari, ANDHRA PRADESH, India

LENORA INSTITUTE OF DENTAL SCIENCES
🇮🇳Godavari, ANDHRA PRADESH, India
DrALLURI SRI NEHA RAJU
Principal investigator
8500757898
dr.nehaalluri@gmail.com

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