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A clinical trail to study the effects of calcium hydroxide and biodentin as pulp capping agents when used alone or in combination with laser

Efficacy of calcium hydroxide and biodentin with or without Diode and Er:YAG Laser assisted direct pulp capping treatment - A randomised controlled study - NIL

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/10/074592
Enrollment
120
Registered
2024-10-01
Start date
Unknown
Completion date
Unknown
Last updated
2024-10-14

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

Conditions

Health Condition 1: K040- Pulpitis

Interventions

Intervention1: calcium hydroxide and diode laser calcium hydroxide and Er:YAG laser biodentin and diode laser biodentin and Er:YAG laser: diode laser and Er:YAG laser used for photobiomodulation for 6

Sponsors

Dr K Rashmi
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: tooth responding positively to cold test with reversible pulpitis permanent teeth with closed apices and carious exposure not larger than 2 mm in diameter tooth with pulpal bleeding controlled within 10 minutes after pulp exposure teeth that can be restored with composite, amalgam

Exclusion criteria

Exclusion criteria: tooth with associated pain, swelling, pus discharge, fistula or abnormal mobility teeth with periapical changes, internal or pathologic external root resorption, calcification or pulp canal obliteration

Design outcomes

Primary

MeasureTime frame
patient will be evaluated for vitality test, intact coronal restoration, presence or absence of pain/swellingTimepoint: patient will be evaluated for vitality test, intact coronal restoration, presence or absence of pain/swelling at baseline, one month, three months, six months and one year follow-up

Secondary

MeasureTime frame
radiographic evaluation for presence or absence of periapical changes will be doneTimepoint: radiographic evaluation for presence or absence of periapical changes at baseline, one month, three months, six months & one year follow up will be done

Countries

India

Contacts

Public ContactDr K Rashmi
rashmiendo@gmail.com9741113002

Outcome results

None listed

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