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NCT Number: NCT05221450

Factors Affecting the Endodontic Treatment Outcome

The aim of this prospective cohort observational study is: (i) to assess the endodontic treatment outcome in a private specialist endodontic office in Slovenia; (ii) to estimate the effect of various pre-, intra- and postoperative factors onto endodontic treatment outcome.

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Key information

Conditions

Apical Periodontitis Apical Cyst Apical Granuloma Bone Cysts Cysts Jaw Cysts Jaw Diseases Mouth Diseases Musculoskeletal Diseases Neoplasms Odontogenic Cysts Periapical Diseases Periapical Granuloma Periapical Periodontitis Periodontal Cyst Periodontal Diseases Periodontitis Radicular Cyst Stomatognathic Diseases

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Odontos, specialistična zobna ambulanta, d.o.o.

Ljubljana, 1000, Slovenia

Location status: Recruiting

Location contact

Janja Jan, Prof.

CONTACT

+386 1 5222770

Rok Juric, DMD

CONTACT

[email protected]

+386 1 2323231

Rok Juric, DMD

PRINCIPAL_INVESTIGATOR

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

patients referred to the private endodontic specialist office for endodontic treatment
written informed consent was obtained prior beginning of the treatment.

Exclusion criteria

preoperative advanced periodontal disease
prior microsurgical root-end resection performed
apices of the tooth were not clearly discernible on any of periapical radiographs
endodontic treated teeth were extracted for non-endodontic reason
the patient did not attend a follow-up examination.

Treatment and study plan

primary endodontic treatment

Procedure

Other names: secondary endodontic treatment

Primary outcomes

Treatment outcome based on strict combined radiographic and clinical criteria

Time frame: 1-4 years postoperatively

Successful treatment outcome is defined as an absence of radiographic sign of apical periodontitis (periapical index PAI <= 2) and clinical signs of inflamation (swelling, sinus tract, tenderness to periapical palpation and percussion, pain) on follow-up examination 1-4 years postoperatively

Study contacts

Contact information is provided by the study sponsor or research team.

Janja Jan, Prof.

CONTACT

+386 1 522 2770

Rok Juric, DMD

CONTACT

[email protected]

+386 1 2323231

Sponsors and collaborators

Lead sponsor

Odontos, Specialisticna Zobna Ambulanta, d.o.o.

Other

Collaborators

University of Ljubljana, Faculty of Medicine

Registry information

Important dates

Study start: 2008
Primary completion: 2027
Study completion: 2028
First posted: Feb 3, 2022
Registry last updated: Apr 9, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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