Development of socket Fit material preventing blood flow during Dental procedures.

DEVELOPMENT OF BIOACTIVE SOCKET FIT HEMOSTAT CUM GRAFT FOR DENTAL APPLICATIONS

Status

Active, not recruiting

Phases

Phase 2

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2021/11/038175

Enrollment

Registered

2021-11-22

Start date

Unknown

Completion date

Unknown

Last updated

2022-02-21

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

Conditions

Health Condition 1: K041- Necrosis of pulp

Interventions

Intervention1: Hemostat made up of gelatine and strontium bioglass: Placement of socket fit hemostat containing gelatine and strontium bioglass in the extraction socket for 1,2,3months Control Interv

Eligibility

Inclusion criteria

Inclusion criteria: Patients undergoing extraction for pulp and periapical diseases.

Exclusion criteria

Exclusion criteria: Patients with any systemic illness will be excluded.

Design outcomes

Primary

Measure	Time frame
Hemostat is expected to exhibit improved hemostasis, antimicrobial efficacy and bone regenerating capability.Timepoint: 1,2,3 months	—

Secondary

Measure	Time frame
Hemostat is expected to exhibit better bone regenerating capability.Timepoint: 1,2,3 months	—

Countries

India

Contacts

Public ContactDr Ramya Ramadoss

SRM DENTAL COLLEGE

ramyaresearch26@gmail.com8825876700

Outcome results

None listed

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