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Clinical evaluation of Polyethylene and Glass Fiber reinforced cuspal coverage restoration in root canal treated teeth.

Clinical Evaluation of Polyethylene and Glass-Fibre Reinforced Cuspal Coverage Restorations as Definitive Post-Endodontic Restorations: A Randomized Parallel Clinical Trial - NIL

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2026/04/108719
Enrollment
96
Registered
2026-04-20
Start date
Unknown
Completion date
Unknown
Last updated
2026-04-27

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

Conditions

Health Condition 1: K044- Acute apical periodontitis of pulpal origin Health Condition 2: K045- Chronic apical periodontitis Health Condition 3: K040- Pulpitis

Interventions

Intervention1: Polyethylene Fiber group, Ribbond: All permanent molar teeth which have undergone standardized root canal therapy will be considered for post endodontic cuspal coverage restoration. The

Sponsors

All India Institute of Medical Sciences, Jodhpur
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.Patients aged 18-60 years 2.Good oral hygiene 3.Root canal treated teeth 4.Mature permanent maxillary/ mandibular molars 5.Root canal treated teeth in the Conservative Dentistry and Endodontics Department of AIIMS Jodhpur 6.No associated pathologic mobility of the tooth 7.Healthy patients without systemic diseases or allergic reactions (ASA I and ASA II)

Exclusion criteria

Exclusion criteria: 1.Patients aged less than 18 years or more than 60 years 2.Teeth with pathologic mobility 3.Patients with systemic diseases 4.Pregnant or lactating women. 5.Patients allergic to materials used in the study 6.Patients with evidence of parafunctional habits 7.Individuals not giving written consent 8.Retreatment cases 9.Radiographic evidence of resorption, root fracture, calcification, advanced bony destruction.

Design outcomes

Primary

MeasureTime frame
To determine which fibre reinforcement material provides superior clinical efficacy and overall restoration quality as cuspal coverage definitive restoration in endodontically treated molar teeth according to the modified United States Public Health Service (USPHS) criteria.Timepoint: Baseline, 3 months, 6 months, 12 months

Secondary

MeasureTime frame
To comparatively evaluate type of failure (repairable v/s irrepairable) of two different cuspal coverage restorations.Timepoint: Baseline, 3 months, 6 months, 12 months

Countries

India

Contacts

Public ContactDr Shikha A S

All India Institute of Medical Sciences, Jodhpur

kumarpr@aiimsjodhpur.edu.in9818402220

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: May 1, 2026