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AzTrials

Post Operative PainNCT04767399

Comparison of Postoperative Pain After Instrumentation in Different Visits With Different Single File Systems.

A study testing protaper next in people with Post Operative Pain, run by Riyadh Elm University at 1 site in Saudi Arabia.

Unknown status

Status not confirmed. The sponsor has not verified this record for over two years, so it may be out of date.

Official record
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Trial summary

Comparison of Postoperative Pain after Root Canal preparation, in Single and Multiple Visits, with Reciprocating and Rotary Single-File Systems: A Randomized Clinical Trial. Aim:1. Compare between the postoperative pain after root canal preparation, in single and multiple visits. 2. Read more about this study

Who is it for?
Ages 19 to 60 yearsHealthy volunteers can take part
Conditions the study is for
Post Operative Pain
What is being tested?
protaper next
Could I receive a placebo?
No, everyone receives an active treatment
How many people
160 participants
Where
1 siteSaudi Arabia
Study dates
10 Sep 2020to 10 Nov 2021
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 19 to 60 years
  • All sexes
  • Healthy volunteers accepted
  • Adult

Who may be able to join

  • a. All permanent teeth diagnosed with vital or non-vital pulps and need nonsurgical root canal treatment.
  • Symptomatic, Asymptomatic maxillary and mandibular teeth with apical radiolucency c. All males and females with age between 19 to 60 years.

Who cannot join

  • a. Teeth with Previously treated b. Teeth need surgical treatment. c. Primary teeth. d. Patients with sinus tract, periapical abscess and who had previously medications.

Trial locations and contacts

1 site in 1 country.

Yahia Alyami contact

Saudi Arabia1 site, 1 recruiting
  • Yahia Abdullah Alyami

    Riyadh, 23323

    Shibu Thomas Mathew, 0534014050, smathew@riyadh.edu.sa

    Recruiting

Other trials in Saudi Arabia

About this study

Official title: Comparison of Postoperative Pain After Root Canal Preparation, in Single and Multiple Visits, With Reciprocating and Rotary Single-File Systems: A Randomized Clinical Trial.

Comparison of Postoperative Pain after Root Canal preparation, in Single and Multiple Visits, with Reciprocating and Rotary Single-File Systems: A Randomized Clinical Trial.

Aim:1. Compare between the postoperative pain after root canal preparation, in single and multiple visits.

  1. To assess the influence of reciprocating and rotary single-file systems instrumentation on post-operative pain.
Read the detailed description

Subjects allocation and randomization method:

  • All diagnoses and treatment procedures will be performed by a single operator in one visit or multiple visits to eliminate or minimize individual variability in the treatment between clinicians.
  • Total of 160 patients, as per the inclusion criteria will be intervened. This will be divided into two groups as follows:
  1. Group A (n=80) single visit.
  2. Group B (n=80) multiple visits.
  • Group A and B will be subdivided into two groups (each group=40) based on the motion of the files to be used either Reciprocation EOF (Edge one Fire file) or Rotational motion PN (ProTaper Next files). Each subgroup will be divided based on either the tooth is vital or non-vital (each subgroup=20) as shown in study design (Figure 1). (Figure 1)
  • A pulpal and periapical diagnoses will be done for each tooth on taking careful history, clinical and radiographic examination based on the American Association of Endodontists (AAE 2008) diagnostic guidelines.
  • The treatments in groups A or B by ProTaper Next or Edge one Fire will be randomized with sequentially numbered opaque sealed envelopes (SNOSE) with 40 patients in PN group and 40 patients in EOF group with allocation sequence and assigning to intervention which will be done by blinded second investigator at the time of cleaning and shaping, concealed from operator to reduce bias.

2.3. Treatment protocol Endodontic therapy consisted of local anesthesia (2% lidocaine with epinephrine 1:100,000 (Xylocaine; Dentsply Pharmaceutical, York, PA) administration and rubber dam isolation followed by access cavity preparation. A size # 10 stainless steel hand K-file (Dentsply) will be used to check the patency of canal. Root ZX II apex locator (J Morita Corp, Kyoto, Japan) will be used to determine the working length which will further confirmed using periapical radiographs After working length determination, the canal will be enlarged to size # 15 using stainless steel hand K-files (Dentsply). At this stage, randomization will be carried out by second investigator based on SNOSE method and patients will be assigned to two different rotary systems, namely, PN and EOF for cleaning and shaping. The patient will be blinded to the type of rotary system used for cleaning and shaping.

Systems Used for Cleaning and Shaping:

Reciprocating motion single file system (n=40): The canals in this group will be instrumented with an engine driven reciprocation motion using an Edge one Fire files (EOF) (EdgeEndo, Albuquerque, New Mexico) with the same preset program specific for the WaveOne Gold instruments, because Edge One Fire has no preset motion and manufacturer declare its full compatibility with WOG counter-clock wise reciprocating motion with an engaging angle of 150° and a disengaging angle of 30° at 300 rpm using an X-Smart Plus endodontic motor (Dentsply Maillefer) with S (20 .06) or P (25 .06) for narrow or severely curved canals and M (35 .04) or L (45 .03) for wide canals.

Rotation motion multiple file system (n=40): The canals in this group will be instrumented with an engine driven rotational motion using a ProTaper Next (PN, Dentsply Sirona Endodontics, Ballaigues, Switzerland) in continuous rotary motion at the speed of 300 rpm and torque 2 Ncm with X1 (17 0.4) and X2 (25 0.6) used for preparation of narrow and curved canals, using X3 (30 0.6), X4 (40 .06) and X5 (50 .06) for wide canals.

Irrigation Protocol:

The same irrigation protocol will be applied in all groups; 2.5% sodium hypochlorite (NaOCl) will be delivered using disposable syringes and a 31-G side-vented needle (NaviTip needle; Ultradent Products Inc, South Jordan, UT) inserted into the canal 3 mm short of the WL between each instrument change. A total of 25 mL 2.5% NaOCl will be delivered per canal. The smear layer formed during chemo-mechanical preparation will be removed by rinsing the canal with 1 mL 17% EDTA and leaving the canal filled with this solution for 1 minute. Patency of the apical foramen will be maintained during all the techniques by introducing a #10 or #15 K-type file (Dentsply) to a point 1 mm beyond the WL at each instrument change. The root canals will be thoroughly dried with paper points after irrigation and before obturation.

Obturation Techniques:

The canals will be subsequently filled with the gutta-percha cones of the respective systems and AH-plus sealer (Dentsply Maillefer) using the continuous wave of condensation technique ??? Excess gutta-percha will be removed with hot instrument and the coronal gutta-percha was vertically condensed. The gutta-percha level will be reduced using hot plugger to a depth of 2 mm from the CEJ.

The access cavity will be closed by Cavit and GIC

2.4. Assessment of post-operative pain and statistical analysis All the participants will be received a card containing VAS (visual analogue scale) to assess pain levels after root canal treatment at 12 h, 24 h and 48 h. According to this scale, the level of pain will be documented in the range of 0-10 numerically and verbally as no pain (0), mild pain (1, 2), moderate pain (3-5), sever pain (6, 7), very severe pain (8), and worst pain possible (9, 10). All the participants will be explained about the scale verbally before the start of the procedure.

Patients will be contacted over telephone by the same clinician at 12, 24 and 48 h time periods and ask to describe the general feeling in the area of the treated tooth, the presence, absence, and intensity of the pain numerical and verbal, and intake of analgesics if any. The information so obtained will be recorded at each follow-up period. None of the patients will be prescribed with medication immediately after the treatment. They will be asked to call the clinician by telephone if they feel any discomfort in the treated area at any point of the follow-up time. If patient complained of pain, then the clinician will prescribe ibuprofen 400 mg as over-the-counter drug.

Data Analysis: Responses of participants to the visual analogue scale and verbal pain scale will be entered into a data spreadsheet software. Differences in post-operative pain between different instruments and different visits will be analyzed using a combination of parametric and non-parametric inferential analysis methods.

Being tested
protaper next
Medical subject headings
Pain, Postoperative

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • protaper nextBehavioural

    Also called Edge-one fire

    rotary systems used on patients need root canal treatment

Study groups in NCT04767399
Study groupRoleWhat they receive
Single visitExperimentalroot canal treatment will be done in one visit
Receives: Behavioral: protaper next
multiple visitExperimentalroot canal treatment will be done in multiple visit
Receives: Behavioral: protaper next

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Visual analogue scale

    appointment treatment at 24 month [ Time Frame: 12, 24, 48, h ] where 0 out of 10 scale will indicates no pain and 10 out of 10 indicates worse pain

    Measured: 24 months

Secondary outcomes (1)
  1. Verbal analogue scale

    appointment treatment at 24 month [ Time Frame: 12, 24, 48, h ] where 0 out of 10 scale will indicates no pain and 10 out of 10 indicates worse pain

    Measured: 24 moths

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted23 Feb 2021
  2. Study start10 Sep 2020
  3. Primary completion10 Sep 2021 (estimated)
  4. Study completion10 Nov 2021 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Masking
Triple blind
Who is masked
Participant, Investigator, Outcomes assessor
Enrolment
160 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT04767399
Sponsor's protocol ID
FPGRP/2020/497
Status last verified
Feb 2021
First submitted
12 Feb 2021
Last updated
3 Mar 2021
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No

Questions about this trial

What is this clinical trial studying?

A study testing protaper next in people with Post Operative Pain, run by Riyadh Elm University at 1 site in Saudi Arabia.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 2 inclusion and 1 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: status not confirmed, as of the sponsor's last update on 3 Mar 2021. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Saudi Arabia. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

Results are not available in the source record.

How can a doctor refer a patient or contact the research team?

Contact Yahia Alyami (0566415159, yahya.a.alyami2019@student.riyadh.edu.sa), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Visual analogue scale (time frame: 24 months). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 3 Mar 2021.

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