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Clinical and radiographic evaluation of bone powder with membrane and bone powder with connective tissue in the treatment of bone loss of bifurcation molars

Clinical and radiographic evaluation of Bio-Gen with Biocollagen and Bio-Gen with connective tissue in treatment of class II Furcation defects

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT201102195861N1
Enrollment
24
Registered
2011-05-25
Start date
2009-12-17
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

furcation grade II IN modrate chronic periodontitis patient. Chronic periodontitis

Interventions

Intervention 1: Test group: Bio-Gen, connective tissue Surgical Procedures: sulcular incision, reflection of the flap, granulation tissue debridment, thorogh scaling & rootplanning, normal salin irrig
Treatment - Surgery
Test group: Bio-Gen, connective tissue Surgical Procedures: sulcular incision, reflection of the flap, granulation tissue debridment, thorogh scaling & rootplanning, normal salin irrigation. Each furc
Control group: Biogen/Biocollagen Surgical Procedures: sulcular incision, reflection of the flap, granulation tissue debridment, thorogh scaling & rootplanning, normal salin irrigation. Each furcation

Sponsors

Babol University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 139 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: =18 years of age and in good general health; good oral hygiene after initial periodontal therapy; mandibular molar with a buccal or lingual degree II furcation defect with =3 mm of horizontal probing depth (HPD); vital teeth or non-vital teeth treated endodontically with clinical or radiographic evidence of periapical pathology; and tooth mobility not to exceed Miller Class II. Exclusion criteria: drugs interfere with periodontal healing; contraindications to periodontal surgery; smokers; caries or restoration of furcation; vital teeth or non-vital teeth treated endodontically with clinical or radiographic evidence of periapical pathology; more than miller class II mobility; cervical enamel projection or another teeth anatomical anomaly

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Furcation to base defect. Timepoint: first surgery/6 month later. Method of measurement: periodontal probe.;Furcation to alveolar crest. Timepoint: first surgery/6 mounth later. Method of measurement: periodontal probe.;Furcation vertical component. Timepoint: first surgery/6 mounth later. Method of measurement: periodontal probe.;Furcation horizontal component. Timepoint: first surgery/6 mounth later. Method of measurement: periodontal probe.

Secondary

MeasureTime frame
Probing depht. Timepoint: just before first surgery/ just before 6 month later. Method of measurement: periodontal probe.;Vertical attachment level. Timepoint: just before first surgery/just before second surgery. Method of measurement: periodontal probe.;Horizontal probing depth. Timepoint: just before first surgery/just before second surgery. Method of measurement: periodontal probe.;Gingival recission. Timepoint: just before first surgery/just before second surgery. Method of measurement: periodontal probe.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr. Avideh Maboudi

Sari dentistry faculty

avideh48188@yahoo.com+98 15 1324 4894

Outcome results

None listed

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