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Reparative/regenerative endodontics - a retrospective clinical study to determine the success rate

Reparative/regenerative endodontics - a retrospective clinical study to determine the success rate

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
DRKS
Registry ID
DRKS00034480
Enrollment
25
Registered
2024-07-15
Start date
2024-05-14
Completion date
Unknown
Last updated
2025-10-06

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

Conditions

K04

Interventions

Group 1: Test subjects with intervention of regenerative endodontic treatment after pulp necrosis

Sponsors

LMU Klinikum - Poliklinik für Zahnerhaltung und Parodontologie
Lead Sponsor

Eligibility

Sex/Gender
All
Age
6 Years to No maximum

Inclusion criteria

Inclusion criteria: - Tooth with necrotic pulp at the start of treatment - Root growth not yet completed, apex at least 1 mm open - Consent of the patient / legal guardian to participate in the study - Patient has reached the age of 6 years

Exclusion criteria

Exclusion criteria: - Patients who are unable to give consent due to a disability - Patients with chronic systemic diseases - Allergy to an antibiotic that is used - Periodontal disease - Teeth with root fracture at initial presentation - Signs of internal or external resorption at the start of treatment - Drug, alcohol consumption - Nicotine abuse - Lack of compliance - No consent to study participation by patient or legal guardian

Design outcomes

Primary

MeasureTime frame
Success rate (absence of symptoms, further apexogenesis) of the regeneratively endodontically treated teeth 18 months postoperatively (assessed on the basis of various clinical and radiological parameters)

Secondary

MeasureTime frame
Discolouration and success of restorative therapy of regeneratively endodontically treated teeth 18 months postoperatively

Countries

Germany

Contacts

Public ContactKarin Huth

LMU Klinikum - Poliklinik für Zahnerhaltung und Parodontologie

Karin.Huth@med.uni-muenchen.de+49 89 44005 9411

Outcome results

None listed

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