Usage of palatal connective tissue graft in treatment of vertical alveolar bone defects

The effect of palatal connective tissue graft usage with and without periosteum as a membrane along with Bio-Oss in treatment of vertical alveolar bone defects

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

IRCT

Registry ID

IRCT2012101611133N1

Enrollment

Registered

2013-01-31

Start date

2012-04-03

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

Chronic Periodontitis. Chronic periodontitis

Interventions

Intervention 1: Palatal connective Tissue graft with periosteum as a membrane. Intervention 2: Palatal connective Tissue graft without periosteum as a membrane.

Treatment - Surgery

Palatal connective Tissue graft with periosteum as a membrane

Palatal connective Tissue graft without periosteum as a membrane

Eligibility

Sex/Gender

All

Age

20 Years to 70 Years

Inclusion criteria

Inclusion criteria: Inclusion Criteria: Plaque Index 25% or less before surgery; teeth with mobility of Miller grade III or less; Vital teeth or nonvital teeth with proper enbdodntic treatment; patients with moderate to severe chronic periodontitis; radiologic approval of a pair of interdental vertical bone defects in two non-adjacent teeth; Clinical attachment loss more than 5millimeteres; defect depth must be at least 3millimeters; intrabony two or three walls defects. Exclusion Criteria: Patients with any systemic disorders; pregnant and breast feeder patients; Systemic antibiotic usage in the last three months; abnormal platelet count in the last month before surgery; Grade III of Furcation involvement; History of periodontal surgery in the last six months.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

Measure	Time frame
Probing Pocket depth. Timepoint: 0 and 6 months. Method of measurement: per millimiters by means of a UNC-15 Periodnotal Probe.;Clinical Attachment Level. Timepoint: 0 and 6 months. Method of measurement: per millimiters by means of a UNC-15 Periodnotal Probe.;Gingival margin status. Timepoint: 0 and 6 months. Method of measurement: per millimiters by means of a UNC-15 Periodnotal Probe.;Defect Bone Fill. Timepoint: 0 and 6 months. Method of measurement: per millimiters by means of a UNC-15 Periodnotal Probe.;Crestal Bone Status. Timepoint: 0 and 6 months. Method of measurement: per millimiters by means of a UNC-15 Periodnotal Probe.;Amount of defect resolve. Timepoint: 0 and 6 months. Method of measurement: per millimiters by means of a UNC-15 Periodnotal Probe.	—

Measure

Time frame

Probing Pocket depth. Timepoint: 0 and 6 months. Method of measurement: per millimiters by means of a UNC-15 Periodnotal Probe.;Clinical Attachment Level. Timepoint: 0 and 6 months. Method of measurement: per millimiters by means of a UNC-15 Periodnotal Probe.;Gingival margin status. Timepoint: 0 and 6 months. Method of measurement: per millimiters by means of a UNC-15 Periodnotal Probe.;Defect Bone Fill. Timepoint: 0 and 6 months. Method of measurement: per millimiters by means of a UNC-15 Periodnotal Probe.;Crestal Bone Status. Timepoint: 0 and 6 months. Method of measurement: per millimiters by means of a UNC-15 Periodnotal Probe.;Amount of defect resolve. Timepoint: 0 and 6 months. Method of measurement: per millimiters by means of a UNC-15 Periodnotal Probe.

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Countries

Iran (Islamic Republic of)

Contacts

Public ContactMohamadreza Ghafari

Islamic Azad Dental School Khorasgan Branch, (Isfahan), Iran

shahabgh1982@gmail.com+98 31 1535 4001

Outcome results

None listed

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