Evaluation of changes in extraction socket of tooth after filling with tooth powder mixed with blood derived product

Phase 4

Completed

• Conditions: Health Condition 1: R69- Illness, unspecified

• Registration Number: CTRI/2019/10/021714
• Lead Sponsor: All India Institute of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Completion: 2023-12-08
• Last Update Posted: 4 March 2024

Recruitment & Eligibility

• Status: Completed
• Sex: Not specified
• Target Recruitment: 46

Inclusion Criteria

b)Patients who have a clinically determined need for extraction of single rooted non-molar tooth (root or crown fractures, non-restorable caries and residual roots). followed by an implant supported restoration

c)Patients who will be available for further follow up.

d)Adequate restorative space for implant-supported restoration

e)Presence of at least one tooth on each side to the tooth to be extracted.

f) = 10-mm distance of alveolar bone crest from the base of the socket.

g)Root location and angulation that would be consistent with the subsequent implant placement.

Exclusion Criteria

a)Inability or anticipated failure to maintain adequate oral hygiene

b)Pregnant or lactating moth¬ers

c) Patients with other systemic conditions (uncontrolled diabetes, unstable bleeding disorders, active infectious diseases; hepatitis, tuberculosis, HIV etc.) that could affect the healing ability of wound.

d)Mental disabilities that may hinder participation.

e)Active immunosuppressive therapy, cancer therapy and/or radiation to the oral cavity within the past 6 months

f)Patients with acute dental infection of bone and ankylosed teeth.

g)Conditions/medications contraindicated for bone regeneration (e.g. methotraxate, cyclosporine A, steroids, bisphosphonates).

h)Multirooted teeth because of the potential for presence of interradicular bone that might be harvested as part of the core biopsy procedure.

i)Loss of more than 50% of buccal plate at the time of extraction

Study & Design

• Study Type: Interventional
• Study Design: Not specified