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A study of the feasibility of testing pulpotomy treatment for toothache in primary dental care

Pulpotomy for the management of Irreversible Pulpitis in mature teeth - (PIP Trial) feasibility study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN17973604
Enrollment
40
Registered
2021-01-28
Start date
2021-04-01
Completion date
Unknown
Last updated
2024-10-21

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

Conditions

Tooth decay (irreversible pulpitis) in adult pre/molar teeth Oral Health Pulpitis

Interventions

Dentists (GDPs) from 10 dental practices will be trained to deliver the pulpotomy treatment. Each participating dental practice will be asked to recruit 4 eligible patients to receive pulpotomy treatm

Sponsors

University of Dundee
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Adults (16 years and older) with symptoms indicative of irreversible pulpitis [as defined by ESE (10)] in a pre/molar tooth with deep caries and or a deep restoration

Exclusion criteria

Exclusion criteria: 1. Tooth with immature roots, clinical or radiographic signs of a necrotic pulp, or a poor prognosis (e.g. internal or external resorption) 2. Presence of a sinus, tenderness to percussion, buccal tenderness, pathological mobility or evidence of pathology on a periapical radiograph 3. Insufficient tooth tissue for a restoration 4. All treatment delivered under a private contract

Design outcomes

Primary

MeasureTime frame
1. Number of GDPs recruited to take part in the study by month 13 2. Proportion of GDPs recruited achieving success in pre-specified clinical criteria (access cavity preparation, adaption of the biodentine material, adequate final restoration) during their training 3. Proportion of radiographs that show compliance with intervention delivery using pre-specified clinical criteria by month 13 4. Proportion of patients satisfied with care measured using the Patient-Reported Experience Measures (PREMs) outlined in the NHS England Guide for Commissioning Dental Specialties (30) at up to 1-month post-intervention 5. Mean number of eligible patients per month by month 13

Secondary

MeasureTime frame
There are no secondary outcome measures

Countries

United Kingdom

Contacts

Public ContactThibault Colloc
tcolloc001@dundee.ac.uk+44 (0)1382 385645

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Feb 18, 2026