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Comparative evaluation of two root-filling materials on post-operative pain in patient with primary endodontic disease

Comparative evaluation of the effect of calcium silicate based and epoxy resin based root canal sealer on postoperat�±ve pa�±n in patients with primary endodontic lesion: a random�±zed clinical study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2022/03/041430
Enrollment
40
Registered
2022-03-28
Start date
Unknown
Completion date
Unknown
Last updated
2022-10-17

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 Health Condition 2: K00-K95- Diseases of the digestive system

Interventions

Intervention1: Nishika Canal Sealer BG (Nippon Shika Yakuhin, Yamaguchi, Japan): CS-BG was developed from BG-based biomaterials and originally intended for both dental pulp and bone regeneration thera
Paste A consists of fatty acids, bismuth subcarbonate, and silica dioxide, whereas Paste B consists of magnesium oxide, calcium silicate glass (a type of BG), and silica dioxide, etc. Duration: 7 day

Sponsors

Dr Supreet Kaur
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: ïÆ?Ë?Healthy individuals without any medical history requiring root canal treatment. ïÆ?Ë?Age from 18 years and above. ïÆ?Ë?First and second molars indicated for root canal treatment with negative response on electric pulp test and cold test ïÆ?Ë?Necrosed teeth with primary endodontic lesion size ïÆ?Ë?Patient who give consent for the treatment.

Exclusion criteria

Exclusion criteria: ïÆ?Ë?Tooth with Root fractures, ïÆ?Ë?Teeth requiring retreatment and previously accessed teeth. ïÆ?Ë?Tooth with large periapical lesion ïÆ?Ë?Tooth with primary perio and secondary endodontic lesions ïÆ?Ë?Patients with the history of antibiotic consumption within past one month, history of analgesic intake within past 24 hours ïÆ?Ë?Patients with known history of allergy

Design outcomes

Primary

MeasureTime frame
To detect post-operative senstivityTimepoint: To detect post-operative senstivity at 24 hr, 48 hr and 7 days

Secondary

MeasureTime frame
NILTimepoint: NIL

Countries

India

Contacts

Public ContactDr SUPREET KAUR

KM SHAH DENTAL COLLEGE

drkishankv@yahoo.co.in8141787335

Outcome results

None listed

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