Effectiveness of Regenerative material in procedures correcting recessed Gums

Efficacy of Tissue Engineered Scaffold in Recession Coverage: A Randomized Clinical Trial - NIL

Status

Active, not recruiting

Phases

Phase 2Phase 3

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2024/09/073701

Enrollment

Registered

2024-09-10

Start date

Unknown

Completion date

Unknown

Last updated

2024-09-16

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: K060- Gingival recession

Interventions

Intervention1: Tissue engineered scaffold: Tissue-engineered scaffold containing gelatin methacrylate with fibroblast growth factor-2 is used in gingival recession coverage. Control Intervention1: Sub

Eligibility

Inclusion criteria

Inclusion criteria: Class I/II Millers Recession defects were included. Full mouth plaque and bleeding scores are less than 20 percent. Vital or Root canal-treated tooth with no associated endodontic pathology.

Exclusion criteria

Exclusion criteria: Systemically unstable patients or immunocompromised individuals. patients with a history of pregnancy or lactation and a history of periodontal surgery within the last year of enrollment.

Design outcomes

Primary

Measure	Time frame
1. Clinical evaluation of Plaque scores 2. Evaluation of Clinical attachment level 3. Early wound healing index(Marini et al) 4. Wound healing index(Huang et al 2005) 5. Percentage of root coverage obtained postoperativelyTimepoint: Baseline, 1 week, 3rd week,1 month and 3rd month	—

Secondary

Measure	Time frame
NilTimepoint: Nil	—

Countries

India

Contacts

Public ContactPriyadarshini M

King George Medical University

rameshwarisinghal@kgmcindia.edu9837400562

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026