Skip to content

Comparasion of Success Rate of Pulpotomy with Biodentine Using PRF Membrane and Collagen scaffold in Permanent Molars

Comparative Evaluation of Success Rate of Pulpotomy with Biodentine Using PRF Membrane and Collagen scaffold in Cariously Exposed Permanent Molars: A Double blinded Randomized Controlled Clinical Trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2023/03/050834
Enrollment
48
Registered
2023-03-20
Start date
Unknown
Completion date
Unknown
Last updated
2024-04-29

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

Conditions

Health Condition 1: K029- Dental caries, unspecified

Interventions

Intervention1: PULPOTOMY USING PRF AND BIODENTIN, PULPOTOMY USING PRF BIODENTIN AND COLLAPLUG: PULPOTOMY WILL BE PERFORMED USING PRF AND BIODENTIN AS PULPTOMY AGENT IN ONE GROUP AND IN OTHER GROUP USI

Sponsors

SGT UNIVERSITY
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Periodontally healthy maxillary and mandibular permanent molars Radiographic carious exposure of pulp Age criteria- patients ranging from 25-45 years of age will be included in the study Positive response to vitality tests • Symptoms of symptomatic irreversible pulpitis

Exclusion criteria

Exclusion criteria: Immunocompromised patients Patients having negative response to vitality tests Tooth previously accessed Neurologic/ Psychiatric patient Association of periapical lesion visible on the radiograph. • Cases in which the bleeding could not be controlled up to 5 minutes • Internal/ external resorption • Abnormal mobility • Immature apex

Design outcomes

Primary

MeasureTime frame
Spontaneous pain and sensitivity following the treatment will also be recorded. Pain and sensitivity occurring after the treatment during the follow up period will also be recorded. Tenderness to percussion will be evaluated. Timepoint: 1 DAY, 2 DAYS AND 7 DAYS

Secondary

MeasureTime frame
Periapical index will be compared with the baseline for radiographic evaluation Timepoint: 3 MONTH, 6 MONTH, 12 MONTH

Countries

India

Contacts

Public ContactDR MAMTA SINGLA

SGT UNIVERSITY

MAMTA.SINGLA@SGTUNIVERSITY.ORG9891381349

Outcome results

None listed

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