Skip to content

a clinical trial to compare the results obtained between two surgical procedures used for regenerating lost gum

comparative evaluation of coronally advanced flap with platelet rich fibrin versus sub-epithelial connective tissue graft in the treatment of gingival recession with Quasi experimental design

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2011/10/002071
Enrollment
10
Registered
2011-10-17
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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

Conditions

Health Condition 1: null- need a dental surgery to regenerate lost gums

Interventions

Intervention1: Coronally advanced flap with Platelet rich fibrin: With two vertical incisions, delineate the flap. These incisions should go beyond the mucogingival junction. Make an internal bevel in

Sponsors

Dr Anoop s
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Bilateral isolated Miller Class I and II recession defects recession depths ≥2 mm systemic health age 18 years to 45 years those consenting to participate in the study

Exclusion criteria

Exclusion criteria: previous surgical attempt to correct gingival recession smokers poor Oral hygiene index Psychiatric disorders pregnancy molar or premolar teeth with furcation involvement. Pathologic mobility of teeth Uncooperative patients.

Design outcomes

Primary

MeasureTime frame
Clinical attachment level clinical probing depth width of keratinized tissue vertical gingival recession depth gingival/mucosal thickness WOUND HEALING INDEX (WHI) MEASUREMENT OF POST-OPERATIVE DISCOMFORT Timepoint: Clinical attachment level baseline ,4 & 9 months clinical probing depth baseline ,4 & 9 months width of keratinized tissue baseline ,4 & 9 months vertical gingival recession depth baseline, 1 & 2 weeks,1,4 & 9 month gingival/mucosal thickness baseline ,4 & 9 months WOUND HEALING INDEX (WHI)1& 2 week MEASUREMENT OF POST-OPERATIVE DISCOMFORT 1 & 2 week, 1 month

Secondary

MeasureTime frame
ESTHETIC OUTCOME MEASUEMENTTimepoint: after 9 months

Countries

India

Contacts

Public ContactDr Anoop S
sebapazhoor@pazhoor.com04712439631

Outcome results

None listed

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