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Role of Nanofibrous scaffolds and I-PRF in Vital pulp therapy of permanent teeth

OUTCOMES OF VITAL PULP THERAPY IN PERMANENT TEETH USING NANOFIBROUS SCAFFOLDS AND I-PRF: A RANDOMISED CONTROLLED STUDY - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/09/074173
Enrollment
45
Registered
2024-09-23
Start date
Unknown
Completion date
Unknown
Last updated
2024-10-14

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

Conditions

None listed

Interventions

Intervention1: Nanofibrous scaffolds: Nanofibrous scaffolds will be placed over exposed pulp Control Intervention1: Injectable PRF: Injectable PRFwill be placed over exposed pulp

Sponsors

None listed

Eligibility

Inclusion criteria

Inclusion criteria: Healthy patient with pin-point exposed mature permanent teeth, with caries or accident-induced pulp exposure will be included in the study.

Exclusion criteria

Exclusion criteria: 1.The patient with history of systemic disease that interferes with pulp healing. 2.The tooth which has clinical signs and symptoms of irreversible pulpitis, e.g., spontaneous throbbing pain, tenderness to percussion, abnormal tooth mobility, swelling, or sinus tract. 3.Radiographic evidence of internal or external resorption, inter-radicular bone loss, or periapical pathology. 4.The tooth which is non-restorable.

Design outcomes

Primary

MeasureTime frame
Pulp vitality Dentin Bridge Formation Pain relief and symptom management Timepoint: Baseline, 1 & then 3 month—

Secondary

MeasureTime frame
Signs of regeneration are seenTimepoint: 6 months—

Countries

India

Contacts

Public ContactDrRamesh Bharti

King Georges Medical University

rakeshanita10@yahoo.in9415281156

Outcome results

None listed

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