Skip to content

FULL PULPOTOMY IN MATURE PERMANENT TEETH WITH IRREVERSIBLE PULPITIS: A STUDY USING TWO BIOACTIVE MATERIALS

FULL PULPOTOMY USING TWO BIOACTIVE MATERIALS IN MATURE PERMANENT TEETH DIAGNOSED WITH SYMPTOMATIC IRREVERSIBLE PULPITIS: A RANDOMIZED CLINICAL TRIAL - NIL

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/02/081323
Enrollment
80
Registered
2025-02-25
Start date
Unknown
Completion date
Unknown
Last updated
2025-09-15

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

Conditions

None listed

Interventions

Intervention1: Two interventional groups are present ie.Theracal PT group and MTA Putty group: The oral cavity will be rinsed with 0.2% chlorhexidine solution for 30 sec to minimize microbial contamin

Sponsors

BHOJIA DENTAL COLLEGE AND HOSPITAL BADDI
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.Teeth with symptomatic irreversible pulpitis with (spontaneous, lingering pain response to cold or electric pulp testing, nocturnal pain that can be mild to moderate.) 2.Medically healthy patients range between 18- 65 years of age 3.Restorable tooth with probing pocket depth and mobility within normal limits. 4.Extremely deep caries extending to pulp chamber 5.Patients who agree to written informed consent 6.Periapical index PAI score 1

Exclusion criteria

Exclusion criteria: 1.Immature teeth 2.Teeth with apical resorption 3.No signs and symptoms of irreversible pulpitis 4.Non restorable teeth 5.Uncontrollable bleeding following pulpotomy lasting more than 10 min. 6.Insufficient bleeding due to necrosis 7.Presence of sinus tract or swelling 8.Allergy to local anesthetic 9.Patients on analgesics, anti-inflammatory drugs & antibiotics 10.PAI score >1

Design outcomes

Primary

MeasureTime frame
Primary objective will be to evaluate the effectiveness of two materials as pulpotomy agents in mature permanent teeth and compare the success rate of these materials in terms of clinical and radiographic evaluation at 12 month follow up.Timepoint: 12 months

Secondary

MeasureTime frame
Secondary objective will be to evaluate reduction of preoperative pain after pulpotomy & whether any difference observed between the materials tested.Timepoint: 12 months

Countries

India

Contacts

Public ContactAmbika Bhardwaj

BHOJIA DENTAL COLLEGE AND HOSPITAL BHUD

amitapsk2002@yahoo.com9878027370

Outcome results

None listed

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