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Microbial assessment in different sealing materials in dental implants

Microbial assessment and quantification following placement of different sealing materials at the screw abutment connection under loading conditions in dental implants: A double blind randomized controlled trial - NIL

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/06/068596
Enrollment
90
Registered
2024-06-07
Start date
Unknown
Completion date
Unknown
Last updated
2024-06-24

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

Conditions

Health Condition 1: K068- Other specified disorders of gingiva and edentulous alveolar ridge

Interventions

Intervention1: temporary filling composite: Intervention group will have Light-curing temporary filling composite - ReTemp LC Flow as sealing agent of implant abutment screw hole. This material has “s

Sponsors

ICMR
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.Patients having edentulism / missing teeth coming to outpatient department of Bharati Vidyapeeth Deemed to be university dental college and hospital, Pune. 2. Healthy adult population above 18 years of age. 3. Patients who are willing to be part of the study and give consent for same.

Exclusion criteria

Exclusion criteria: 1. Fully dentate patients. 2. Patients who are not willing to be part of study. 3. Patients having any uncontrolled systemic condition who cannot undergo implant surgical procedures, having history of smoking in the past one year.

Design outcomes

Primary

MeasureTime frame
Bacterial genome count in sealing agentsTimepoint: At time of implant placement

Secondary

MeasureTime frame
1.Peri – implant health. 2.Survival of dental implants during course of study. 3.Failure rate of dental implants. 4.Technical complications: screw loosening, screw fracture, abutment fracture, loss of prosthesis 5.At present there is no defined consensus regarding the most suitable sealing material for use in implant abutment screw hole. Outcome of our study may help reduce this ambiguity. 6.The outcome is likely to provide additional information regarding peri-implant disease and bacterial cause of subsequent implant failure.Timepoint: 03 months after loading

Countries

India

Contacts

Public ContactDr Sarah Mariam

Bharati Vidyapeeth deemed to be university dental college and hospital, Pune

sarah.mariam@bharatividyapeeth.edu9540068535

Outcome results

None listed

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