Clinical trial Recruiting at 2 sites Interventional Ages 18 to 65

Effect of NiTi File Systems and XP-Endo Finisher on Postoperative Pain After Root Canal Treatment

Official title: EVALUATION OF THE EFFECT OF RECIPROCATING AND ROTARY NICKEL-TITANIUM FILE SYSTEMS USED IN COMBINATION WITH XP-ENDO FINISHER ON POSTOPERATIVE PAIN FOLLOWING ROOT CANAL TREATMENT

Run by Eskisehir Osmangazi University · NCT07642596 · Data updated 2026-11-12

This study tests whether different NiTi file systems and the XP-Endo Finisher can reduce pain after endodontic treatment in adults.

More Postoperative Pain After Endodontic Treatment trials

Quick facts

Study typeInterventional
Ages18 Years to 65 Years
SexAll
Enrollment80 (estimated)
SponsorEskisehir Osmangazi University
Academic / other
Locations2 sites (Eskişehir, Odunpazarı and 1 other locations)
StatusRecruiting
StartedFebruary 13, 2026
Main results expectedFebruary 28, 2027
Study endsApril 30, 2027
Registry record updatedJune 11, 2026
Trial IDNCT07642596 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Adults aged 18-65 requiring root canal treatment for mandibular molars with pulpal necrosis and periapical radiolucent lesions.

Probably not a fit

Patients with non-necrotic pulps, acute infections, or anatomy unsuitable for the tested systems may not experience pain reduction.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This interventional study compares two rotary NiTi file systems (FKG Race Evo and One Reci) and their combinations with an irrigation-activation device (XP-Endo Finisher) to see which approach best manages postoperative pain after root canal treatment in molar teeth. Participants are adults aged 18-65 with pulpal necrosis and chronic apical periodontitis undergoing endodontic therapy. The study uses randomized or controlled assessment of pain outcomes following treatment with each file system and activation combination, aiming to understand the influence of instrumentation and irrigation enhancements on pain and healing. The protocol emphasizes minimizing apical extrusion and improving disinfection to potentially lower postoperative discomfort. The results may add clinically relevant information to optimize endodontic procedures and patient comfort.

Why it matters

Potential benefit: If successful, patients may experience less postoperative pain and a smoother recovery after root canal treatment.

How similar studies have gone: Previous work suggests that instrumentation and activation devices can influence postoperative pain, but findings vary by system; this study explores this specific combination.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Age 18-65 years. Healthy volunteers. Mandibular molar teeth with pulpal necrosis, asymptomatic status, chronic apical periodontitis, and periapical radiolucent lesion.

Written informed consent.

Exclusion Criteria:

* Patients who have taken analgesic or anti-inflammatory drugs within the last 12 hours.

Patients with allergy to non-steroidal anti-inflammatory drugs or local anesthetics.

Pregnant or lactating patients. Patients with a history of gastrointestinal diseases. Patients using opioid medications. Teeth with calcified canals, resorptive defects, or complex root canal anatomy. Patients with severe periodontal disease. Patients with acute or chronic apical abscess or signs of systemic infection. Immunosuppressed patients.

Where it's running

  • Eskişehir Osmangazi University
    Eskişehir, Odunpazarı, Turkey (Türkiye)
    Recruiting
  • Eskişehir Osmangazi University
    Eskişehir, Odunpazarı, Turkey (Türkiye)
    Recruiting

Study contacts

  • Principal investigator: Büşra Öztürk — Eskisehir Osmangazi University
  • Study coordinator: Büşra Öztürk, Research Assistant
  • Email: oztrkbusra95@gmail.com
  • Phone: +905546810288

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.