Efficacy of connective tissue graft as a membrane and ABBM With and without PRP in treatment of intrabony defects

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

IRCT

Registry ID

IRCT201104116167N1

Enrollment

Registered

2011-10-27

Start date

2010-03-11

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

Alveolar vertical bony defects.

Interventions

Intervention 1: Connective Tissue as a Membrane And ABBM(anorganic bovine bone ) With PRP . Intervention 2: Connective Tissue as a Membrane And ABBM(anorganic bovine bone ) Without PRP .

Treatment - Surgery

Connective Tissue as a Membrane And ABBM(anorganic bovine bone ) With PRP .

Connective Tissue as a Membrane And ABBM(anorganic bovine bone ) Without PRP .

Eligibility

Sex/Gender

All

Age

20 Years to 70 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: No amount of 25% or less plaque before surgery . Teeth with a mobility of less than 3 Miller . Endodontic treatment of teeth or vital teeth. . Patients with moderate to advanced chronic periodontitis and at least one pair of radiographic lesions in non-adjacent teeth, and vertically between the minimum level of attachment to the CEJ from the first phase of treatment is 5 mm. The depth of the defect during surgery is at least 3 mm. The vertical wall is 2 or 3 bone lesions. Exclusion criteria: 1. Systemic diseases 2. Pregnancy and breast feeding 3. The systemic use of antibiotics in the past three months 4. Abnormal platelet count before surgery in a month 5. Furcation involvement and grade 3 or 4 6. Other forms of chronic periodontitis periodontitis to 7. History of periodontal surgery in 6 Months

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

Measure	Time frame
Pocket depth. Timepoint: Before and 6 months after. Method of measurement: Probe and Acrylic stent.;Clinical attachment level. Timepoint: Before and 6 months after. Method of measurement: Probe and Acrylic stent.;Free ginigival margin position. Timepoint: Before and 6 months after. Method of measurement: Probe and Acrylic stent.;Alveolar crest position. Timepoint: During and 6 months after. Method of measurement: Probe and Acrylic stent.;Defect depth to Stent. Timepoint: Before and 6 months after. Method of measurement: Probe and Acrylic stent.	—

Measure

Time frame

Pocket depth. Timepoint: Before and 6 months after. Method of measurement: Probe and Acrylic stent.;Clinical attachment level. Timepoint: Before and 6 months after. Method of measurement: Probe and Acrylic stent.;Free ginigival margin position. Timepoint: Before and 6 months after. Method of measurement: Probe and Acrylic stent.;Alveolar crest position. Timepoint: During and 6 months after. Method of measurement: Probe and Acrylic stent.;Defect depth to Stent. Timepoint: Before and 6 months after. Method of measurement: Probe and Acrylic stent.

—

Countries

Iran (Islamic Republic of)

Contacts

Public ContactOmid Moghaddas

Dental Faculty,Islamic Azad University,Khorasgan ,Isfahan

hmonn555@yahoo.com+98 31 1535 4066

Outcome results

None listed

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