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Post-Operative Pain Evaluation After Using Different Single-file Root Canal Preparation System: A Randomized Clinical Study

T

Tanta University

Status

Completed

Conditions

Root Canal Treatment

Treatments

Device: Hyflex EDM , The XP-endo Shaper, Primary WaveOne Gold

Study type

Interventional

Funder types

Other

Identifiers

NCT06207019
#R-END-1-20-5

Details and patient eligibility

About

The goal of this clinical trial is to assess post-operative pain following root canal preparation using various single-file systems

Full description

The goal of this clinical trial is to assess post-operative pain following root canal preparation using various single-file systems.Postoperative pain assessment was done by an independent evaluator with no knowledge of the group under investigation. The visual Analogue Scale (VAS) was employed. Patients could put a mark anywhere on the VAS sheet with values ranging from 0 to 100 mm [10].

  • Score 0: No pain (between 0 and 4 mm) the tooth after treatment felt normal, and no discomfort was reported by the patients.
  • Score 1: Recognizable, mild pain (between 5 and 44 mm), not requiring analgesics.
  • Score 2: Moderate pain (between 45 and 74 mm) that is uncomfortable but bearable (when analgesics were taken, the pain was successfully reduced).
  • Score 3: Severe pain (between 75 and 100 mm) painful to endure (pain was not relieved by taking analgesics).

The patients in this study were not aware of the preparation system used during treatment. Following treatment, three readings were taken at 24, 72, and 7 days. Each patient carried a VAS form, and reminder calls were made to record pain levels and return the form filled out completely

Enrollment

30 patients

Sex

All

Ages

20 to 40 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • • Teeth with a single root canal with nearly the same apical diameter (#15)

    • Vital pulp exposures due to caries or trauma with asymptomatic pulpitis
    • Restorable teeth

Exclusion criteria

  • • Patients with immune deficiencies or systemic illnesses

    • Pregnant women
    • Cases of re-treatment
    • Symptomatic non-vital teeth that require root canal therapy
    • Presence of root resorption
    • Teeth with anatomic variations
    • A cute periapical abscess cases with pus discharge
    • A patient who has several teeth that need to be treated in order to eliminate the likelihood of pain referral
    • Periodontal diseases
    • Patients on analgesics, anti-inflammatory drugs, sedatives, or antibiotics seven days before therapy

Trial design

Primary purpose

Health Services Research

Allocation

Randomized

Interventional model

Crossover Assignment

Masking

Double Blind

30 participants in 3 patient groups

Hyflex EDM
Active Comparator group
Description:
Hyflex EDM One File (25/) with variable taper was used in continuous rotation at 500 rpm and 2.5 Ncm in a circumferential brushing action in the coronal and middle thirds, then in a pecking action for three to five cycles until the WL was reached.
Treatment:
Device: Hyflex EDM , The XP-endo Shaper, Primary WaveOne Gold
The XP-endo Shaper
Active Comparator group
Description:
The XP-endo Shaper (30/0.01) was used in rotation mode at 800 rpm and 1.0 Ncm torque. Long, gentle strokes with amplitudes of 3-4 mm were used to go down to adjusted WL in three to five cycles. After it reached the WL over the adjusted WL, it was subjected to five more up-and-down motions.
Treatment:
Device: Hyflex EDM , The XP-endo Shaper, Primary WaveOne Gold
Primary WaveOne Gold
Active Comparator group
Description:
Primary WaveOne Gold (25/07) was applied three times in a reciprocating motion; a gradual in-and-out pecking movement was utilized as directed by the manufacturer till the WL was reached.
Treatment:
Device: Hyflex EDM , The XP-endo Shaper, Primary WaveOne Gold

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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