A Study to check Result of Treating Painful Decayed Teeth using Two Different Techniques of Pulp Removal.

Outcome Assessment of Partial and Full Pulpotomy Using Biodentine in Cariously Exposed Mature Molars With Irreversible Pulpitis: A Clinical Study

Status

Active, not recruiting

Phases

Phase 2

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2019/12/022559

Enrollment

Registered

2019-12-30

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: R52- Pain, unspecified

Interventions

Intervention1: Partial pulpotomy: Partial pulpotomy using biodentine in Cariously Exposed Mature Molars With Irreversible Pulpitis Control Intervention1: Full pulpotomy: Full pulpotomy using biodentin

Eligibility

Inclusion criteria

Inclusion criteria: Clinical inclusion criteria 1.The patient should be more 18 years old 2.Patient should have non-contributory Medical history 3.Tooth with deep Class I caries presenting with signs and symptoms indicative of irreversible pulpitis. 4.History of spontaneous pain and/or nocturnal pain which aggravates on lying down. 5.Patient reporting with spontaneous pain and/or with sharp and lingering pain upon cold testing using Endo-Ice and early exaggerated response with electric pulp testing. 6.A restorable tooth with probing pocket depth( 7.Complete caries removal will result in pulpal exposure. 8.Bleeding from the pulp exposure site stops with 2.5-3% NaOCl irrigation within 10 minutes. Radiological inclusion criteria 1.Extremely deep caries (penetrating the entire thickness of the dentine without a radiopaque zone separating the lesion from the pulp) 2.Absence of periapical or furcation changes in the radiograph

Exclusion criteria

Exclusion criteria: 1.Tooth having unexposed pulp after complete caries removal. 2.Tooth exhibiting uncontrolled pulpal haemorrhage during the procedure lasting more than 10 minutes. 3.Exposed pulp tissue appearing necrotic, judged by absence of bleeding or presence of pale necrotic pulp tissue. 4. Presence of internal or pathologic external root resorption, calcification or pulp canal obliteration.

Design outcomes

Primary

Measure	Time frame
Absence of spontaneous pain and pain during chewing,Lack of swelling and sinus tract, fistulaTimepoint: pre operative, post operative, 2 weeks, 3 months and 6 months of procedure	—

Secondary

Measure	Time frame
No periapical or furcation changes and Absence of internal and/or external root resorption in the radiograph Timepoint: pre operative, post operative, 2 weeks, 3 months and 6 months of procedure	—

Countries

India

Contacts

Public ContactDr Ashima Jassal

Maulana Azad Institute Of Dental Sciences

sangeeta.talwar@gmail.com9654700950

Outcome results

None listed

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