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Completed

NCT Number: NCT05747183

Effect of ProTaper Ultimate System on Post-endodontic Pain

This clinical trial aims to compare the effect of Pro Taper Ultimate and Pro Taper Gold files on post-endodontic pain in molars with symptomatic apical periodontitis.

The main question it aims to answer is:

If there is a difference in post-endodontic pain intensity following root canal preparation using Pro Taper Ultimate and Pro Taper Gold files in molar diagnosed with symptomatic apical periodontitis?

Participants will undergo root canal treatment using Pro Taper Ultimate and Pro Taper Gold files.

Researchers will compare [Pro Taper Ultimate and Pro Taper Gold files] to see the intensity of post-endodontic pain

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Key information

Age range

18 year–70 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Gulf Medical University

Ajman, 4184, United Arab Emirates

About this study

The study will be conducted on 40 first mandibular molars; with 20 first mandibular molars in each group (n=20). The patient will be asked to pick an opaque sealed envelope that will contain a number from 1 to 2. The resultant number will determine in which group the participants will be placed.

Group I: Root canal preparation using Pro Taper Ultimate. Group II: Root canal preparation using Pro Taper Gold.

Procedural steps:

  • Vitality will be assessed using cold tests and electric pulp testing before the procedure is carried out. Besides, mobility, palpation, and percussion tests will be done to assess periapical health. In order to ensure that the cold and electrical pulp tests are working, and a response is elicited, both tests will be carried out on patients not included in the study.
  • All the patients will receive local anesthesia: 2% lidocaine with 1:100,000 epinephrine.
  • Each tooth will be isolated using a rubber dam, and the access cavity will be prepared using a round bur (no.4) and tapered fissure diamond bur under copious water.
  • After removal of coronal pulp tissues using a sterile excavator, the working length will be determined with stainless steel hand K-files size #10 and the use of an apex locator and confirmed using intraoral periapical radiographs.
  • Hand instrumentation to 15-size K files.
  • Group I will be prepared using ProTaper Ultimate files.
  • Group II will be prepared using ProTaper Gold files.
  • Apical patency will be maintained throughout the shaping procedure using the #10 file between each instrument.
  • All the canals will be irrigated with 10 mL of 3% NaOCl between each file during the whole preparation procedure.
  • All the root canals will be obturated directly after preparation.
  • All the teeth will be restored using resin composite restoration.

Who can participate

Healthy volunteers accepted: Yes

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

Inclusion criteria

  • Patient was diagnosed with symptomatic irreversible pulpits and symptomatic apical periodontitis.
  • 18-70 years old patients
  • Permanent mandibular first molars.
  • Teeth with a fully matured root.
  • Restorable teeth indicated for endodontic treatment.
  • Healthy patients.

Exclusion criteria

  • Complex root canal morphology
  • Calcified roots.
  • Teeth with internal and external resorption.
  • Medically compromised patients.
  • Restricted mouth openings (trismus).

Treatment and study plan

ProTaper Ultimate

Procedure

Root canal preparation using ProTaper Ultimate files.

ProTaper Gold

Procedure

Root canal preparation using ProTaper Gold files.

Primary outcomes

  1. The level of post-endodontic pain

    Time frame: 24 hours

    Evaluation of the pain intensity using the Visual Analogue Scale. The Visual Analogue Scale measures pain intensity. The Visual Analogue Scale consists of a 10cm line, with two endpoints representing 0 ('no pain') and 10 ('pain as bad as it could possibly be)

  2. The level of post-endodontic pain

    Time frame: 72 hours

    Evaluation of the pain intensity using the Visual Analogue Scale. The Visual Analogue Scale measures pain intensity. The Visual Analogue Scale consists of a 10cm line, with two endpoints representing 0 ('no pain') and 10 ('pain as bad as it could possibly be)

  3. The level of post-endodontic pain

    Time frame: 1 week

    Evaluation of the pain intensity using the Visual Analogue Scale. The Visual Analogue Scale measures pain intensity. The Visual Analogue Scale consists of a 10cm line, with two endpoints representing 0 ('no pain') and 10 ('pain as bad as it could possibly be)

Sponsors and collaborators

Lead sponsor

Gulf Medical University

Other

Registry information

Official study title

Comparison of Post Endodontic Pain for Preparation Using ProTaper Gold and ProTaper Ultimate Systems. A Randomized Clinical Study

Important dates

Study start
2022
Primary completion
2024
Study completion
2024
First posted
Feb 28, 2023
Registry last updated
Sep 4, 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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