A comparative evaluation of De-epithelialized Gingival Graft versus Sub-epithelial Connective Tissue Graft in Treatment Of Single Gingival Recession Using The Coronally Advanced Flap Technique

Status

Recruiting

Phases

Unknown

Study type

Interventional

Source

IRCT

Registry ID

IRCT20101006004877N30

Enrollment

Registered

2022-05-20

Start date

2022-04-20

Completion date

Unknown

Last updated

2022-05-30

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

Conditions

Gingival recession. Gingival recession

Interventions

Intervention 1: Intervention group: Treatment of single gingival recession by using coronally advanced flap with palatal cannective tissue harvested with de epithelialized free gingival graft method.

Eligibility

Sex/Gender

All

Age

18 Years to 60 Years

Inclusion criteria

Inclusion criteria: Age between 18 to 60 years Non-smoker and systemically healthy, No active periodontal disease Presence of at least two single-rooted teeth with Miller class I and/or II (RT1) buccal gingival recession defects =2 mm in depth Full-mouthplaque and bleeding score of 3 mm, Absence of non-carious cervical lesions (NCCLs) and non-detectable cemento-enamel junction (CEJ) at the defect sites No history of previous periodontal plastic surgery at the affected sites Minimum 2.5mm thickness of palatal mucosa

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

Measure	Time frame
Gingival margin level to cej (recession depth). Timepoint: Baseline , 3 and 6 month after surgery. Method of measurement: Periodontal probe.	—

Secondary

Measure	Time frame
Recession width. Timepoint: Baseline , 3 and 6 month after surgery. Method of measurement: Periodontal probe.;Keratinized tissue width. Timepoint: Baseline , 3 and 6 month after surgery. Method of measurement: Periodontal probe.;Clinical attachment level. Timepoint: Baseline , 3 and 6 month after surgery. Method of measurement: Periodontal probe.;Gingival thickness. Timepoint: Baseline , 3 and 6 month after surgery. Method of measurement: Digital caliper and endodontic file.;Probing depth. Timepoint: Baseline , 3 and 6 month after surgery. Method of measurement: Periodontal probe.;Patient satisfaction. Timepoint: 6 Month after surgery. Method of measurement: Visual Analogue Scale.;Pain and discomfort. Timepoint: 1, 2, 3, 7, 14 Days after treatment. Method of measurement: Visual Analogue Scale.;Root Coverage Esthetic Score ( RES ). Timepoint: 6 Month after treatment. Method of measurement: Score of index.;Post operation bleeding. Timepoint: 1, 2, 3, 7, 14 Days after treatment. Method of measurement: Patient two-part response.	—

Measure

Time frame

Recession width. Timepoint: Baseline , 3 and 6 month after surgery. Method of measurement: Periodontal probe.;Keratinized tissue width. Timepoint: Baseline , 3 and 6 month after surgery. Method of measurement: Periodontal probe.;Clinical attachment level. Timepoint: Baseline , 3 and 6 month after surgery. Method of measurement: Periodontal probe.;Gingival thickness. Timepoint: Baseline , 3 and 6 month after surgery. Method of measurement: Digital caliper and endodontic file.;Probing depth. Timepoint: Baseline , 3 and 6 month after surgery. Method of measurement: Periodontal probe.;Patient satisfaction. Timepoint: 6 Month after surgery. Method of measurement: Visual Analogue Scale.;Pain and discomfort. Timepoint: 1, 2, 3, 7, 14 Days after treatment. Method of measurement: Visual Analogue Scale.;Root Coverage Esthetic Score ( RES ). Timepoint: 6 Month after treatment. Method of measurement: Score of index.;Post operation bleeding. Timepoint: 1, 2, 3, 7, 14 Days after treatment. Method of measurement: Patient two-part response.

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Countries

Iran (Islamic Republic of)

Contacts

Public ContactJaber Yaghini

Esfahan University of Medical Sciences

J_yaghini@dnt.mui.ac.ir+98 31 3792 5542

Outcome results

None listed

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