Comparison of pulpotomy in teeth using MTA and biodentine

Not yet recruiting

• Conditions: cariously exposed permanent molars and premolars with clinical features of chronic irriversible pulpitis

• Registration Number: CTRI/2020/03/023766
• Lead Sponsor: Mandeep S Grewal

Brief Summary

cariously exposed mature premolar and molar teeth with irreversible pulpitis were allocated in three groups. in the first group pulpotomy was done using MTA, in the second group pulpotomy was done using biodentine and in the third group root canal treatment was performed and the patients were recalled at subsequent follow up visits for evaluating the post operative pain and success rate of pulpotomy as compared to root canal therapy. groups in which pulpotomy was performed, if reported with pain then root canal therapy was initiated for those patients.

Detailed Description

Not available

Study Timeline

• Last Update Posted: 2020-03-03
• Study Start: 2020-05-03

Recruitment & Eligibility

• Status: Not Yet Recruiting
• Sex: All
• Target Recruitment: 150

Inclusion Criteria

• Periodontally healthy maxillary and mandibuar permanent molars and premolars with the carious exposure of pulp will be included.
• Age criteria- patients ranging from 18 to 69 years of age will be incuded in the study.
• Positive response to vitality tests and a history of pain and presenting symptoms characteristic of symptomatic irreversible pulpitis according to American Association of Endodontics diagnosis terminology, but in the absence of sinus tract or swelling will be included.

Exclusion Criteria

• •Immunocompromised patients •Patients having negative response to vitality tests •Positive history of intake of antibiotics use in the past one month or requiring antibiotic prophylaxis.
• •Tooth previously accessed.
• •Association of periapical lesion visible on the radiograph.
• •Cases in which the bleeding could not be controlled upto fifteen minutes.

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
No post operative pain and successful treatment outcome	1 year

Secondary Outcome Measures

Name	Time	Method
Pain or swelling at follow up visits	1 year, 6 months

Trial Locations

Locations (1)

Faculty of Dental Sciences, Sgt University; 🇮🇳 Gurgaon, HARYANA, India

Faculty of Dental Sciences, Sgt University

🇮🇳Gurgaon, HARYANA, India

Mahak Mitra

Principal investigator

8826827933

mahakmitra.03@gmail.com