clinical trial to study two materials propolis and MTA as DEEP FILLING MATERIAL ON TOOTH

COMPARATIVE HISTOLOGIC ASSESSMENT OF HUMAN PULP RESPONSE TO CAPPING WITH PROPOLIS AND MINERAL TRIOXIDE AGGREGATE A RANDOMIZED CONTROLLED CLINICAL TRIAL

Status

Recruiting

Phases

Phase 1Phase 2

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2011/05/001718

Enrollment

Registered

2011-05-09

Start date

Unknown

Completion date

Unknown

Last updated

2021-11-24

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

Conditions

Health Condition 1: null- -age : 18-25yrs -systemically healthy without caries and periodontitis

Interventions

Intervention1: Propolis: resin 55% essential oil and wax 30% salivary secretion of bees and pollen 5% amino acids and minerals 10% Control Intervention1: Mineral trioxide aggregate: Calcium oxide-50-7

Eligibility

Inclusion criteria

Inclusion criteria: teeth without caries or restoration

Exclusion criteria

Exclusion criteria: patient allergic to pollen and apiary products patients with systemic disease teeth with periodontal involvement

Design outcomes

Primary

Measure	Time frame
inhibition of Inflammatory cell response reparative dentine formationTimepoint: inhibition of inflammatory response and reparative dentine formation 15 to 60 days	—

Secondary

Measure	Time frame
NILTimepoint: NIL	—

Countries

India

Contacts

Public ContactDr Mali G Nair

malignair@gmail.com9495626572

Outcome results

None listed

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