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Laser-Assisted Disinfection With and Without Photobiomodulation in Regenerative Endodontic Procedures for Necrotic Mature Teeth (LASER)

6. november 2026 oppdatert av: mohamed khalid moselhy, Future University in Egypt

Radiographic and Clinical Evaluation of Regenerative Endodontic Procedures in Necrotic Mature Teeth With Apical Periodontitis Using Laser-Assisted Disinfection With and Without Adjunctive Photobiomodulation: A Three-Arm Randomized Clinical Trial

This study will compare three ways of treating adult teeth with a dead nerve (pulp) and an infection at the root tip. All three groups receive a regenerative endodontic procedure, which aims to help healthy tissue grow back inside the tooth. The groups differ in how the root canal is cleaned: (1) standard cleaning without a laser, (2) standard cleaning plus a diode laser to help disinfect the canal, or (3) standard cleaning plus the diode laser plus a single session of low-level light therapy (photobiomodulation) applied over the gum to support healing. Eighty-one patients aged 20 to 40 will be randomly placed into one of the three groups. Healing of the infection at the root tip will be measured with a 3D dental scan (CBCT) before treatment and 12 months later. Pain after treatment, painkiller use, and clinical signs such as swelling, tenderness, and gum pimples (sinus tract) will also be recorded. The study aims to find out whether adding laser treatment, with or without light therapy, improves healing.

Studieoversikt

Studietype

Intervensjonell

Registrering (Antatt)

81

Fase

  • Ikke aktuelt

Kontakter og plasseringer

Denne delen inneholder kontaktinformasjon for de som utfører studien, og informasjon om hvor denne studien blir utført.

Studiekontakt

Studiesteder

    • Cairo Governorate
      • Cairo, Cairo Governorate, Egypt
        • Future University in Egypt
        • Ta kontakt med:

Deltakelseskriterier

Forskere ser etter personer som passer til en bestemt beskrivelse, kalt kvalifikasjonskriterier. Noen eksempler på disse kriteriene er en persons generelle helsetilstand eller tidligere behandlinger.

Kvalifikasjonskriterier

Alder som er kvalifisert for studier

20 år til 40 år (Voksen)

Tar imot friske frivillige

Nei

Kjønn som er kvalifisert for studier

Alle

Beskrivelse

  • Good general health (ASA I or II)
  • Aged 20 to 40 years
  • Both sexes (male and female)
  • Single-rooted mature permanent tooth
  • Negative response to pulp sensibility testing (cold test)
  • Periapical radiolucency ranging from widening of the lamina dura/periodontal ligament space up to a periapical lesion less than 5 mm in diameter on CBCT
  • Restorable tooth with adequate remaining coronal structure and periodontal support
  • Patient agrees to participate and is able to sign informed consent

Exclusion Criteria:

  • Analgesic or antibiotic intake within 12 hours before the procedure
  • Immature teeth
  • Multi-rooted teeth
  • Periapical lesion 5 mm or more in diameter
  • Unrestorable teeth
  • Teeth with vertical root fracture, extensive internal or external resorption, grade 2 or 3 mobility, or non-restorable coronal destruction
  • Previous root canal treatment
  • Systemic conditions or medications affecting healing (for example uncontrolled diabetes, immunosuppression, bisphosphonate therapy)
  • Pregnant or lactating patients
  • Unable to understand the procedure, provide valid consent, or comply with follow-up
  • Known allergy to the irrigants or medicaments used in the protocol

Studieplan

Denne delen gir detaljer om studieplanen, inkludert hvordan studien er utformet og hva studien måler.

Hvordan er studiet utformet?

Designdetaljer

  • Primært formål: Behandling
  • Tildeling: Randomisert
  • Intervensjonsmodell: Parallell tildeling
  • Masking: Dobbelt

Våpen og intervensjoner

Deltakergruppe / Arm
Intervensjon / Behandling
Aktiv komparator: REP's with no laser disinfection (control)

Regenerative endodontic procedure (REP) with conventional chemomechanical preparation only (2.5% sodium hypochlorite, passive ultrasonic activation, 17% EDTA, and sterile saline), followed by a calcium hydroxide intracanal dressing for 2 weeks. At the second visit: EDTA irrigation, induced apical bleeding to form a blood clot, collagen matrix, bioceramic putty barrier, and coronal seal. No laser is used.

Two-visit regenerative endodontic procedure for necrotic mature teeth single root and single canal. Visit 1: access, working length determination, crown-down chemomechanical preparation with 2.5% sodium hypochlorite, passive ultrasonic activation, 17% EDTA, final saline rinse, and calcium hydroxide dressing for 2 weeks. Visit 2: 17% EDTA irrigation, induction of apical bleeding to form a blood clot, collagen matrix, bioceramic putty barrier, and coronal seal with glass ionomer. Performed identically in all three groups.

Eksperimentell: REP's with laser-assisted disinfection, using adjunctive 810 nm diode laser irradiation.

Same REP protocol as the control group, with the addition of 810 nm diode laser disinfection at the first visit after the final saline rinse and before the calcium hydroxide dressing. Continuous wave mode, 1.5 W, 4 cycles of 5 seconds with 20-second intervals, using a 200 micrometer fiber placed 1 mm short of the working length and moved in a slow helical motion from apical to coronal. The canal is irrigated with 5 mL saline after each cycle. The second visit is identical to the control group.

Two-visit regenerative endodontic procedure for necrotic mature teeth single root and single canal. Visit 1: access, working length determination, crown-down chemomechanical preparation with 2.5% sodium hypochlorite, passive ultrasonic activation, 17% EDTA, final saline rinse, and calcium hydroxide dressing for 2 weeks. Visit 2: 17% EDTA irrigation, induction of apical bleeding to form a blood clot, collagen matrix, bioceramic putty barrier, and coronal seal with glass ionomer. Performed identically in all three groups.

Adjunctive canal disinfection at the first visit using an 810 nm diode laser (Elexxion, Germany), continuous wave, 1.5 W, 4 cycles of 5 seconds with 20-second intervals. A 200 micrometer fiber is placed 1 mm short of the working length and moved in a slow helical motion from apical to coronal at about 2 mm per second without touching the canal walls. The canal is irrigated with 5 mL sterile saline after each cycle.

Eksperimentell: REP's with Laser-assisted disinfection and adjunctive photobiomodulation,

Same protocol as the laser-assisted disinfection group, plus a single session of transmucosal photobiomodulation (PBM) delivered at the second visit immediately after placement of the blood scaffold and coronal restoration. 810 nm diode laser, continuous wave, 200 mW, 8 mm tip in contact with the mucosa, applied at four sites per tooth (periapical and cervical regions on the buccal and lingual/palatal sides), 15 seconds and 3 J per site, for a total of 12 J per tooth.

Two-visit regenerative endodontic procedure for necrotic mature teeth single root and single canal. Visit 1: access, working length determination, crown-down chemomechanical preparation with 2.5% sodium hypochlorite, passive ultrasonic activation, 17% EDTA, final saline rinse, and calcium hydroxide dressing for 2 weeks. Visit 2: 17% EDTA irrigation, induction of apical bleeding to form a blood clot, collagen matrix, bioceramic putty barrier, and coronal seal with glass ionomer. Performed identically in all three groups.

Adjunctive canal disinfection at the first visit using an 810 nm diode laser (Elexxion, Germany), continuous wave, 1.5 W, 4 cycles of 5 seconds with 20-second intervals. A 200 micrometer fiber is placed 1 mm short of the working length and moved in a slow helical motion from apical to coronal at about 2 mm per second without touching the canal walls. The canal is irrigated with 5 mL sterile saline after each cycle.

Single session of transmucosal photobiomodulation at the second visit, immediately after placement of the blood scaffold and coronal restoration. 810 nm diode laser, continuous wave, 200 mW, 8 mm tip in contact with the mucosa. Four sites per tooth (periapical and cervical regions on the buccal and lingual/palatal sides), 15 seconds and 3 J per site, for a total of 12 J per tooth.

Hva måler studien?

Primære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Change in periapical lesion volume (mm3) measured on CBCT
Tidsramme: baseline and 12 month

Periapical lesion volume in cubic millimeters measured on cone-beam computed tomography (CBCT) scans (field of view 50 x 50 mm, isometric voxel size 0.125 mm) by a blinded outcome assessor. Change from baseline to 12 months is compared among the three groups.

baseline and 12 month

Sekundære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Postoperative pain intensity (Numeric Rating Scale)
Tidsramme: Preoperative (baseline), 6 hours, 12 hours, 24 hours, 48 hours, and 72 hours

Patient-reported pain on the Numeric Rating Scale from 0 (no pain) to 10 (worst pain imaginable), collected by telephone by a blinded study coordinator.

Preoperative (baseline), 6 hours, 12 hours, 24 hours, 48 hours, and 72 hours
Postoperative analgesic intake
Tidsramme: 6 hours, 12 hours, 24 hours, 48 hours, and 72 hours

Whether any analgesic was taken since the previous assessment, with the number of doses and dose per intake, recorded at each telephone contact.

6 hours, 12 hours, 24 hours, 48 hours, and 72 hours
Resolution of clinical signs and symptoms
Tidsramme: Preoperative (baseline), second visit, 3 months, 6 months, and 12 months

Presence or absence of tenderness to percussion, tenderness to palpation, swelling, and sinus tract, and need for additional intervention, assessed by clinical examination by a blinded examiner.

Preoperative (baseline), second visit, 3 months, 6 months, and 12 months

Samarbeidspartnere og etterforskere

Det er her du vil finne personer og organisasjoner som er involvert i denne studien.

Studierekorddatoer

Disse datoene sporer fremdriften for innsending av studieposter og sammendragsresultater til ClinicalTrials.gov. Studieposter og rapporterte resultater gjennomgås av National Library of Medicine (NLM) for å sikre at de oppfyller spesifikke kvalitetskontrollstandarder før de legges ut på det offentlige nettstedet.

Studer hoveddatoer

Studiestart (Antatt)

1. desember 2026

Primær fullføring (Antatt)

1. desember 2027

Studiet fullført (Antatt)

1. januar 2028

Datoer for studieregistrering

Først innsendt

6. november 2026

Først innsendt som oppfylte QC-kriteriene

6. november 2026

Først lagt ut (Faktiske)

12. november 2026

Oppdateringer av studieposter

Sist oppdatering lagt ut (Faktiske)

12. november 2026

Siste oppdatering sendt inn som oppfylte QC-kriteriene

6. november 2026

Sist bekreftet

1. november 2026

Mer informasjon

Begreper knyttet til denne studien

Plan for individuelle deltakerdata (IPD)

Planlegger du å dele individuelle deltakerdata (IPD)?

NEI

Legemiddel- og utstyrsinformasjon, studiedokumenter

Studerer et amerikansk FDA-regulert medikamentprodukt

Nei

Studerer et amerikansk FDA-regulert enhetsprodukt

Nei

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