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Pulpotomy of carious teeth

Outcome of Biodentine™ full pulpotomy in adult permanent teeth with carious exposures

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN84455971
Enrollment
80
Registered
2017-11-09
Start date
2016-04-01
Completion date
Unknown
Last updated
2018-09-03

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

Conditions

Deep caries, irreversible pulpitis, symptomatic apical periodontitis Oral Health Deep caries, irreversible pulpitis, symptomatic apical periodontitis

Interventions

The following steps are included in this procedure: 1. The carious tooth will be anesthetized using local anesthesia. 2. Full pulpotomy will be performed for the tooth under rubber dam isolation. 3.

Sponsors

Jordan University of Science and Technology
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. The patient should be = 18 years old with non-contributory medical history, either male or female 2. Has a molar tooth with deep caries exposing the pulp or extending = 2/3 into dentine and subsequent clinical pulp exposure 3. Tooth should be vital on cold testing, restorable and free from advanced periodontal disease 4. Clinical diagnosis of irreversible pulpitis with /without periapical rarefaction 5. Soft tissues around the tooth are normal with no swelling or sinus tract 6. Vital bleeding pulp tissue should be present in all canals after complete pulpotomy 7. Haemostatis should be achieved after complete pulpotomy within 6 minutes

Exclusion criteria

Exclusion criteria: 1. Teeth with immature roots 2. Non restorable teeth 3. Negative response to cold testing, presence of sinus tract or swelling 4. No pulp exposure after caries excavation 5. Bleeding could not be controlled after partial pulpotomy in 6 minutes 6. Insufficient bleeding after pulp exposure, the pulp is judged necrotic or partially necrotic

Design outcomes

Primary

MeasureTime frame
1. Clinical success is measured using percussion, palpation, inspection tests of the treated tooth at 6 months, 1 year, 3 years, 5 years post treatment 2. Radiographic success is measured by periapical radiograph at 6 months, 1 year, 3 years, 5 years post treatment

Secondary

MeasureTime frame
Resolution of symptoms are measured using Visual analogue scale and 0-10 scale at 2 days after treatment.

Countries

Jordan

Outcome results

None listed

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