The Comparison of Free gingival unit graft and free gingival graft for the Treatment of Gingival Recession

Status

Active, not recruiting

Phases

Phase 4

Study type

Interventional

Source

IRCT

Registry ID

IRCT201403061760N33

Enrollment

Registered

2014-04-27

Start date

2014-03-11

Completion date

Unknown

Last updated

2018-02-22

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: Case group (free gingival unit graft): the donor gingival unit graft was dissected from the palatal aspect of the maxillary premolars. Care will be taken to obtain a graft thickness of

Treatment - Surgery

Case group (free gingival unit graft): the donor gingival unit graft was dissected from the palatal aspect of the maxillary premolars. Care will be taken to obtain a graft thickness of 1 mm. The graf

Control group ( conventional free gingival graft): the donor palatal graft was harvested from the palate corresponding to the premolar area but ‡2 mm away from the gingival margin. Care will be taken

Eligibility

Sex/Gender

All

Age

18 Years to No maximum

Inclusion criteria

Inclusion criteria: Inclusion criteria: there is a single two-way analysis of facial tissue depth of 2mm = X CEJ on anterior teeth or premolars; putting all subgroup analyzes of Miller class I / II; selected teeth without root fillings and no bleeding after probing; people over 18 years of age; ability to maintain good oral hygiene (% 20 O'Leary plaque score=); sufficient depth of vestibule. Exclusion criteria: pregnancy; interfere with the healing agents (corticosteroids, anti-cancer) or medicines that may lead to gingival enlargement; smoking; administration has banned any local or systemic disease, periodontal surgery; traumatic brushing techniques, brushing hard or abrasive toothpastes; history of periodontal surgery in the area in the past 2 years; the use of removable prosthodontic or orthodontic appliances in the area; known allergies to materials used in surgery.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

Measure	Time frame
Treatment of Gingival Recession. Timepoint: Six months after surgery. Method of measurement: clinical.	—

Secondary

Measure	Time frame
Healing. Timepoint: One, three and six months after surgery. Method of measurement: Indexed repair Landry.;Pain relief after surgery. Timepoint: One, three and six months after surgery. Method of measurement: pain Index (VAS).;Esthetic. Timepoint: One, three and six months after surgery. Method of measurement: Esthetic index (VAS).;Percentage of root coverage (RC). Timepoint: One, three and six months after surgery. Method of measurement: Clinical.;Clinical Attachment Level ( CAL ). Timepoint: Three and six months after surgery. Method of measurement: Mm.	—

Measure

Time frame

Healing. Timepoint: One, three and six months after surgery. Method of measurement: Indexed repair Landry.;Pain relief after surgery. Timepoint: One, three and six months after surgery. Method of measurement: pain Index (VAS).;Esthetic. Timepoint: One, three and six months after surgery. Method of measurement: Esthetic index (VAS).;Percentage of root coverage (RC). Timepoint: One, three and six months after surgery. Method of measurement: Clinical.;Clinical Attachment Level ( CAL ). Timepoint: Three and six months after surgery. Method of measurement: Mm.

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Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr. Mohadese Yazdan Panah

Dental School, Babol University of Medical Sciences

mohadese.yazdanpanah@yahoo.com+98 11 1229 1408

Outcome results

None listed

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