Use of a new biomaterial in oral surgery procedure to reduce pain and improve healing

Comparative evaluation of the efficacy of a novel biomaterial in wound healing and postoperative pain management in alveoloplasty. - NIL

Status

Active, not recruiting

Phases

Phase 2

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2025/04/084935

Enrollment

Registered

2025-04-16

Start date

Unknown

Completion date

Unknown

Last updated

2025-04-28

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

Conditions

None listed

Interventions

Intervention1: Novel Biomaterial: Novel Biomaterial is an intermeshing of chitosan acting as a scaffold impregnated with AgNP and 2% lidocaine that will serve the purpose of wound healing and antibact

Eligibility

Inclusion criteria

Inclusion criteria: Patients requiring bilateral alveoloplasty procedure

Exclusion criteria

Exclusion criteria: 1. Patients with any systemic diseases 2. Patients with known psychological disorder 3. Patients with history of allergy to lignocaine.

Design outcomes

Primary

Measure	Time frame
1. Wound Healing 2. PainTimepoint: 1. Wound Healing -1 week 2. Pain - 1 week	—

Secondary

Measure	Time frame
1. Rescue medications requirementTimepoint: 1 week	—

Countries

India

Contacts

Public ContactManoj Bafna

DR D Y Patil Dental College And Hospital

kalyani.bhate@dpu.edu.in9822099311

Outcome results