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A clinical trial to compare two techniques in the treatment involving partial removal of pulp

Comparative evaluation of conventional and laser technique with biodentine and theracal lc in partial pulpotomy of mature permanent teeth - RCT

Status
Active, not recruiting
Phases
Phase 1
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2021/08/035343
Enrollment
52
Registered
2021-08-02
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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

Conditions

None listed

Interventions

Intervention1: Evaluation of laser technique with biodentine and theracal lc in partial pulpotomy of mature permanent teeth: After local anesthesia the teeth were properly isolated under rubber dam an

Sponsors

Thivyashankari T
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Unrestored permanent teeth with deep caries in occlusal and proximal surface with extension more than 2/3 dentin in close proximity to the pulp Vital teeth; no history of spontaneous pain; history of mild, dull, and tolerable pain associated with eating and drinking cold and hot drinks The vitality of the teeth before the treatment is determined by cold tests with ethyl chloride, heat by gutta-percha, palpation, percussion, and the absence of any radiological symptoms in periapical radiographs. Pain caused by a cold or heat triggered pulp test should not persist after the stimulus is removed In periapical radiography, there is no evidence of endodontic lesion or calcified pulp with normal lamina dura and periodontal ligaments.

Exclusion criteria

Exclusion criteria: Restored teeth and in teeth where there are any clinical symptoms and history of spontaneous pain and continued pain caused by a cold or heat and pulp test Endodontic pathological changes in periapical region with lamina dura disruption and periodontal ligament expansion internal or external resorption pulp calcification and in teeth where there is bleeding for more than 3 minutes in the exposure area

Design outcomes

Primary

MeasureTime frame
elimination of signs and symptoms with no evidence of further periapical pathological findings in the radiographTimepoint: 3 months,6 months, 12 months

Secondary

MeasureTime frame
no evidence of progression of periapical pathological findings in the radiographTimepoint: 3 months, 6 months, 12 months

Countries

India

Contacts

Public ContactThivyashankariT

Faculty of Dental Sciences,IMS,BHU

thivyashankari@gmail.com7339568671

Outcome results

None listed

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