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Root canal treatment outcomes using different ways to clean and disinfect teeth, including light technology (LASER)

Outcome of non-surgical endodontic treatment using different irrigant activation techniques

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN91211125
Enrollment
264
Registered
2025-04-08
Start date
2023-01-10
Completion date
Unknown
Last updated
2025-09-08

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

Conditions

Healing of apical periodontitis (due to primary endodontic infection) Oral Health

Interventions

Patients with root canal disease (also known as pathology of endodontic origin) who meet the inclusion criteria and not the exclusion criteria will be randomly allocated to one of three groups. The en

Sponsors

University of Central Lancashire
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Patients either male or female over the age of 18 (who can consent for themselves) in good general health 2. Patients with clinical symptoms of pathology of endodontic origin who need endodontic treatment 3. All anterior and posterior teeth included in study

Exclusion criteria

Exclusion criteria: 1. External or internal root resorption 2. Pregnant women, in view of requirements for radiographs. 3. Patients younger than 18 years. 4. Patients unable to give consent. 5. Patients who have been administered antibiotics in the previous month. 6. Immunocompromised patients.

Design outcomes

Primary

MeasureTime frame
Healing outcome after non-surgical treatment measured using clinical examination (intact restoration, no fistulas or swelling, no mobility of the teeth or tenderness to percussion) and radiographical assessment using periapical radiographs and CBCT (absence or reduction of any radiolucencies or widening of the periodontal ligament space and vertical or horizontal fractures and absence of external root resorption) at 12 months and 24 months

Secondary

MeasureTime frame
1. Patient self-reported pain measured using VAS (Visual Analogue Scale) pre-operatively, and then day 1, 3, 5, 7 and 14 following the treatment 2. Patients' quality of life measured using OHIP-14 preoperatively and at year 1 and year 2

Countries

England, United Kingdom

Contacts

Public ContactShalini;Tiago Kanagasingam;Pimentel

;

skanagasingam1@uclan.ac.uk;t.pimentel@ucl.ac.uk+44 7398276670;-

Outcome results

None listed

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