Skip to content

A Study Comparing a Bioactive Restorative Material (Bioactive Activa) and a Resin-Modified Glass Ionomer Cement for Back Teeth in beta Thalassemia Patients in CuttackOdisha

Comparative evaluation of bioactive restorative material (Bioactiva Active) and a resin-modified glass Ionomer Cement in posterior restorations among beta-thalassemia patients visiting a tertiary care centre in Cuttack Odisha A Randomized Control Trial - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2026/05/110362
Enrollment
110
Registered
2026-05-11
Start date
Unknown
Completion date
Unknown
Last updated
2026-06-01

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

Conditions

Health Condition 1: K029- Dental caries, unspecified Health Condition 2: D50-D89- Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism

Interventions

Intervention1: Bioactiva Active: patient in intervention group will be restored with Bioactiva Active and reviewed after 6months and 12 months with USPHS criteria Control Intervention1: Resin-modified

Sponsors

SCB DENTAL COLLEGE AND HOSPITAL
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Participants with at least one active carious lesion as defined by Nyvad scores 2 or 3 in posterior tooth (both primary and permanent), receiving routine care at the Thalassemia Clinic of clinical haematology department Children aged 6-15 years Having parental consent

Exclusion criteria

Exclusion criteria: Children with systemic disorders like serious or unstable cardiac, renal, hypertensive, pulmonary, or endocrine disorders Having grossly decayed teeth with more than one-third of the crown structure missing. Tooth involved in the study with periapical pathology

Design outcomes

Primary

MeasureTime frame
Absolute risk difference and relative risk of secondary caries for both the groups at 6 and 12 monthsTimepoint: 6 months and 12 months

Secondary

MeasureTime frame
Absolute risk difference and relative risk for retention, marginal adaptation, color match, and postoperative hypersensitivity will be assessed for both groups at 6 and 12 monthsTimepoint: 6 months and 12 months

Countries

India

Contacts

Public ContactDR HEMAMALINI RATH

SCB DENTAL COLLEGE AND HOSPITAL

hema_hr@rediffmail.com9437225245

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Jun 11, 2026