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Comparative evaluation of Amniotic membrane/Collagen membrane for the management of periodontal intra-bony defects

Comparative evaluation of clinical and radiological parameters following the use of biphasic alloplastic material with Amniotic membrane / Collagen membrane for the management of periodontal intra-bony defects - A prospective double blind randomized controlled clinical trial.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2020/03/024075
Enrollment
40
Registered
2020-03-19
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

Health Condition 1: K053- Chronic periodontitis

Interventions

Intervention1: amniotic membrane: use of amniotic membrane with biphasic calcium phosphate in the management of intrabony defects Control Intervention1: collagen membrane: use of collagen membrane wit

Sponsors

nivedhav
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1 Age 21-50 years 2 Patients with moderate to severe localized periodontitis with a Probing Depth (PD) >=6 mm and an intrabony component of more than 3 mm as detected on Intra oral periapical radiographs (IOPAR) and bone sounding (Sali 2016). 3 Intrabony defect angle of less than 40 degree (Sali 2016). 4 Circumferential defect with interdental intrabony defect depth of more than 3mm will be included. 5 Nonsmoker (Never smoker) or former smoker (Does not smoke now and has not smoked at all for a minimum of the last 12 consecutive months)

Exclusion criteria

Exclusion criteria: 1 Current Smokers (smokers who have smoked more than 100 cigarettes in their lifetime and currently smoke) 2 Systemic chronic conditions known to be associated with periodontitis or with changes in systemic inflammation: Diabetes, Cardiovascular diseases, Rheumatoid Arthritis, Rheumatic Fever, SLE, Malignancy, Respiratory diseases, Renal diseases, Other (e.g., autoimmune diseases, fungal infections, immunological deficiencies, etc.) 3 Pregnant / Lactating mothers 4 Previous History of periodontal treatment at the selected site 5 Teeth with intrabony defect component and furcation involvement were also excluded from the study.

Design outcomes

Primary

MeasureTime frame
Change in Probing Pocket Depth or Clinical Attachment Level and Radiographic bone gainTimepoint: baseline, 1 month, 3 month and 6 month

Secondary

MeasureTime frame
Wound Healing index, Visual Analogue ScaleTimepoint: at 3, 10 days

Countries

India

Contacts

Public ContactNivedhaV

Sri Ramachandra institute of higher education and research

venarun7@gmail.com9445513282

Outcome results

None listed

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