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To evaluate postoperative sensitivity in four different tooth colored materials in patients

To evaluate postoperative sensitivity of posterior composite restorations- In vivo study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2019/10/021552
Enrollment
120
Registered
2019-10-07
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: K025- Dental caries on pit and fissure surface

Interventions

Intervention1: bulk fill composites: Postoperative sensitivity of Bulk fill composite evaluated immediately one day one week one month Control Intervention1: incremental: Postoperative sensitivity o

Sponsors

Sharmila R
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: patients with minimum age of 18 years patients with 12 posterior teeth in occlusion with natural antagonist teeth and adjacent teeth cavity depth of atleast 3 mm

Exclusion criteria

Exclusion criteria: patients needing endodontic treatment nonvital teeth and teeth with periodontal problem patients undergoing orthodontic treatment pregnant and breastfeeding patients allergies to resin based materials those taking anti-inflammatory analgesic or psychotropic drugs

Design outcomes

Primary

MeasureTime frame
there is no significant difference in the postoperative sensitivity of the materials testedTimepoint: Immediate ,one day, one week,one month—

Secondary

MeasureTime frame
none of the materials tested had postoperative sensitivityTimepoint: one day , one week, one month—

Countries

India

Contacts

Public ContactDR A R PRADEEP KUMAR

Thai moogambigai dental college and hospital

arpradeep@vsnl.com9840135711

Outcome results

None listed

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