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Partial Pulpotomy vs Selective Removing in Deep Caries

Selective Caries Removal Versus Partial Pulpotomy in the Treatment of Deep Caries: A Randomized Controlled Trial

Status
Not yet recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07120009
Enrollment
70
Registered
2025-08-13
Start date
2025-09-01
Completion date
2026-12-01
Last updated
2025-08-13

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

Conditions

Deep Dentin Caries in Mature Permanent Teeth

Keywords

Vital pulp therapy, Deep caries, Selective caries removal, Partial pulpotomy

Brief summary

The aim of this study was to compare the one-year results of selective caries removal and partial pulpotomy treatments in terms of pulp survival and the need for further endodontic treatment in deep carious lesions.Individuals aged 18-65 years with medically healthy mature permanent teeth with deep caries will be included. The included teeth will be randomly assigned to the selective caries removal or partial pulpotomy group. Follow-up evaluations will be performed at 6 months and 12 months. The main outcome is pulp survival as determined by clinical and radiographic success.

Interventions

The caries is not completely removed but covered with a remineralizing material. Its purpose is to maintain pulp vitality.

PROCEDUREpartial pulpotpmy

Complete cleaning of the caries resulting in pulp expose. pulp tissue is surgically removed by 1-3 mm.The aim is to remove the inflamed superficial pulp tissue to allow healing from the underlying healthy tissue.

Sponsors

Cukurova University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

* Individuals aged 18-65 * ASA I or II general health status * Deep primary or secondary caries lesion (up to 75% dentin thickness) * Restorable permanent teeth with mature apex * Teeth without clinical and radiographic periapical pathology

Exclusion criteria

* Pregnancy * Periapical lesion * Spontaneous pain or tenderness to palpation * Teeth for which pulp opening or crown/root supported prosthesis is planned * Localized severe periodontitis

Design outcomes

Primary

MeasureTime frameDescription
Assessment of pain6th and 12th monthDetailed medical history * Is the pain constant or intermittent? * How severe is the pain? The outcome will be evaluated using the Visual Analog Scale (VAS), which ranges from 0 to 10, with higher scores indicating a worse outcome.
Periapical pathology6th and 12th monthStandardized digital periapical radiographs will be taken using the long cone paralleling technique to assess periapical status, presence of radiolucent lesions, and periodontal ligament space. Radiographs will be obtained at baseline, 6 months, and 12 months to monitor treatment outcomes and detect any pathological changes.
Tenderness to percussion12th month1. Usually, the back of a dental mirror handle or the handle of a periodontal probe is used. 2. First, vertical percussion (lightly tapping the occlusal surface from above) is performed, followed by lateral percussion (lightly tapping the side of the tooth) if necessary. 3. It is compared with other teeth in the same area. If the pain is only in one tooth, it suggests pathology. 4. The patient describes the pain as aching, discomfort, or severe pain. This severity indicates the severity of the inflamation

Contacts

Primary Contactzeliha g bek kurklu
goncabek@mynet.com+905334500892

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026