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To evaluate and compare postoperative pain and success rate of pulpotomy with Biodentine using diode laser and normal saline in mature cariously exposed permanent molars and premolars.

Comparative Evaluation of Pulpotomy with Biodentine using Diode Laser and Normal Saline in Cariously Exposed Permanent molars and premolars: A Randomized Controlled Trial with One Year Follow Up

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2020/03/023894
Enrollment
150
Registered
2020-03-11
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

None listed

Interventions

Intervention1: nil: nil Control Intervention1: nil: nil

Sponsors

Dr Shipra Jain
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.Periodontally healthy human maxillary and mandibular permanent molars and premolars with the carious exposure of pulp. 2.Age criteria- patients ranging from 18 to 69 years of age. 3.Positive response to sensibility tests and a history of pain, sensitivity and presenting symptoms characteristic of symptomatic irreversible pulpitis according to American Association of Endodontics diagnosis terminology, in the absence of sinus tract or swelling.

Exclusion criteria

Exclusion criteria: 1.Immunocompromised patients. 2.Patients having negative response to vitality tests. 3.Positive history of intake of antibiotics use in the past one month or requiring antibiotic prophylaxis. 4.Tooth previously accessed. 5.Association of periapical lesion visible on the radiograph. 6.Cases in which the bleeding could not be controlled up to eight minutes (in pulpotomy cases only).

Design outcomes

Primary

MeasureTime frame
Patients will be recalled at 3 months, 6 months and 12 months for clinical and radiographic examination and evaluation of functionality of the tooth and integrity of the restoration, to check for presence of any cracks or fractures in the tooth, discoloration of the tooth.Timepoint: Patients will be recalled at 3 months, 6 months and 12 months

Secondary

MeasureTime frame
pain and sensitivity will be scored preoperatively at 24 hours, 48 hours and the seventh day and fourteenth day after the first appointment day on 170 mm HP VAS.Timepoint: pain and sensitivity will be scored preoperatively at 24 hours, 48 hours and the seventh day and fourteenth day after the first appointment day on 170 mm HP VAS.

Countries

India

Contacts

Public ContactDr Shipra Jain

SGT Dental college,Gurugram

drashthaarya@yahoo.co.in9810761757

Outcome results

None listed

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