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Comparison of sticky bone with xenograft for bone regeneration in periodontal defect-A Randomised controlled clinical & radiographic study

Comparative evaluation of efficacy of sticky bone compared to xenograft for the treatment of intrabony defects : A randomized controlled clinical and radiographic study

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2020/03/023751
Enrollment
24
Registered
2020-03-04
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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

Conditions

None listed

Interventions

Intervention1: STICKY BONE: It is a combination of injectable platelet rich fibrin (I-PRF) and bone graft which is used to fill the bone defect. Control Intervention1: XENOGRAFT: It is a bone graft th

Sponsors

NISHANTA BORA
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients with Good physical health and Maintaining good oral hygiene after completion of scaling and root planing will be selected. Patients with attachment loss more than 6 mm at two or more sites will be selected, these sites exhibited the radiographic evidence of defect. Two or three wall intrabony defects will be selected.

Exclusion criteria

Exclusion criteria: Pregnant females and people having allergy to LA & chlorhexidine, antibiotic and analgesic will be excluded.Past or present habit of tobacco chewing or smoking as well as patients having systemic conditions like hypertension and diabetes that will effect the outcome of study will be excluded. patients with Previous history of periodontal surgery and allergy or history of allergy to usage of xenograft will be excluded.

Design outcomes

Primary

MeasureTime frame
The use of sticky bone in the treatment procedure of intrabony defects will help in stabilization of bone graft and therefore will accelerate tissue healing and minimization of bone loss during healing period. This will lead to increase in the relative attachment level, gingival marginal level and % of bone fill in the patient.Timepoint: Patients will be recalled after 7 days post surgery for suture removal. Patients will be recalled every month for six months. At each visit oral hygiene will be reinforced and full mouth supragingival scaling will be done.—

Secondary

MeasureTime frame
Gingival marginal level will be evaluated.Timepoint: Patients will be recalled after 7 days post surgery for suture removal. Patients will be recalled every month for six months. At each visit oral hygiene will be reinforced and full mouth supragingival scaling will be done.—

Countries

India

Contacts

Public ContactNISHANTA BORA

KM SHAH DENTAL COLLEGE AND HOSPITAL

smonali2011@gmail.com9824003228

Outcome results

None listed

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