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Clinical Trials in India / NCT07576439
Recruiting Not applicable

Influence of Keratinized Tissue Width and Attached Gingiva Width on Root Coverage in Patients With Recession Defects: A Prospective Clinical Study

NCT07576439 · tracked via the Priya Life Science India tracker
Sponsor
Postgraduate Institute of Dental Sciences Rohtak
Phase
Not applicable
Started
2026-07-01
Last updated
2026-09-18

Condition(s) studied

Gingival Recessions

Investigational drug(s) / intervention(s)

Vestibular incision subperiosteal tunnel access with connective tissue graft in treating RT 1 gingival recession defects

Vestibular incision subperiosteal tunnel access with connective tissue graft in treating RT 1 gingival recession defects: the aim of this prospective clinical study is to determine if anatomical factors such as keratinized tissue width and attached gingiva width influence recession defects coverage of RT1 recession treated with minimally invasive surgical technique along with connective tissue graft. Keratinized tissue width and attached gingiva width are considered important for maintaining gingival health and long-term stability after root coverage. However, there is limited and unclear evidence on how much keratinized or attached gingiva is actually needed for successful root coverage. Most previous studies have focused on soft tissue thickness rather than these parameters.

Study summary

To evaluate the association between the width of keratinized tissue and attached gingiva with root coverage outcomes in RT1 gingival recession defects of maxillary and mandibular anterior teeth treated with subepithelial connective tissue graft (CTG) using a minimally invasive technique : modified vestibular incision subperiosteal tunnel access(m-VISTA).

OBJECTIVES

1. PRIMARY OBJECTIVES

1. To analyze relation and association at 3 and 6 months outcomes in terms of CRC, mRC and gingival margin position with baseline parameters including width of keratinized tissue and width of attached gingiva, after providing mucogingival plastic surgery in the form of m-VISTA+CTG for the treatment of RT1recession defects.
2. To evaluate 3 and 6 months outcomes (percentage of root coverage, width of keratinized tissue and width of attached gingiva), after providing mucogingival plastic surgery in the form of m-VISTA+CTG for the treatment of RT1recession defects.
3. To access the long-term stability of gingival margin achieved from 3 months to 6 months.
2. SECONDARY OBJECTIVES

1. To access recession depth (RD), recession width (RW), probing pocket depth (PPD), mid buccal clinical attachment loss (bCAL), change in gingival thickness (GT) at baseline, at 3 months and 6 months.
2. To access patient related outcomes measures (PROM) in pain and hypersensitivity in teeth with gingival recession undergoing recession coverage.

Eligibility

Sex
ALL
Min age
18 Years
Max age
60 Years
Healthy volunteers
No
Inclusion Criteria: 1. Patients with Millers class Ⅰ and II / RT1 isolated recession defects in labial maxillary and mandibular anterior teeth region. 2. Recession depth ≥2mm 3. Systemically healthy individuals. 4. Age \>18 years old. 5. Full mouth bleeding and plaque score ≤20% 6. Patients who agreed to participate in the study and signed an informed consent form. Exclusion Criteria: 1. Patients having systemic disease such as hypertension, diabetes, hyperthyroidism or on medication that influence the outcome of periodontal therapy. 2. Patient with active periodontal disease 3. Smokers and tobacco users 4. Mal-aligned tooth with recession. 5. Patients who had already undergone root coverage procedure on the selected site. 6. Pregnant and lactating females 7. Involved tooth with trauma from occlusion. 8. Involved tooth with prosthesis. 9. Endodontically involved/ RCT treated tooth 10. Tooth with cervical abrasion / undetectable CEJ/ carious

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Post Graduate Institute of Dental Sciences Rohtak Haryana Recruiting

More Postgraduate Institute of Dental Sciences Rohtak trials in India

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07576439 on ClinicalTrials.gov ↗ ← All trials in India