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.
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
- Type of treatment
- Lifestyle or therapy programme
- 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
- Recruiting
Yahia Abdullah Alyami
Riyadh, 23323
Shibu Thomas Mathew, 0534014050, smathew@riyadh.edu.sa
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.
- 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:
- Group A (n=80) single visit.
- 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.
- Conditions
- Post Operative Pain
- 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 group | Role | What they receive |
|---|---|---|
| Single visit | Experimental | root canal treatment will be done in one visit Receives: Behavioral: protaper next |
| multiple visit | Experimental | root 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.
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)
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.
- First posted23 Feb 2021
- Study start10 Sep 2020
- Primary completion10 Sep 2021 (estimated)
- Study completion10 Nov 2021 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Post Operative PainStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
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)
Sponsor and investigators
- Lead sponsor
- Riyadh Elm University
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, Yahia Abdullah Alyami, Riyadh Elm University
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
Study at a glance
From the registry record, last updated by the sponsor on 3 Mar 2021. Recruitment status is as the sponsor reported it: confirm with the study team.
- 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.
- ClinicalTrials.gov ID
- NCT04767399
- Acronym / sponsor ID
- FPGRP/2020/497
- Conditions
- Post Operative Pain
- Study type
- Interventional
- Recruitment status
- Unknown status
- Enrolment
- 160 participants (estimated)
- Lead sponsor
- Riyadh Elm UniversityUniversity, hospital or other
- Study start
- 10 Sep 2020 (actual)
- Primary completion
- 10 Sep 2021 (estimated)
- Study completion
- 10 Nov 2021 (estimated)
- First posted
- 23 Feb 2021 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
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.
- To assess the influence of reciprocating and rotary single-file systems instrumentation on post-operative pain.
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:
- Group A (n=80) single visit.
- 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.
Study design
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Triple blind (participant, investigator, outcomes assessor)
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| Single visit | Experimental | Behavioral: protaper nextroot canal treatment will be done in one visit |
| multiple visit | Experimental | Behavioral: protaper nextroot canal treatment will be done in multiple visit |
Who may qualify
- Ages
- 19 to 60 years
- Sex
- All
- Healthy volunteers
- Accepted
- Age groups
- Adult
Key inclusion criteria (2 listed)
- a. All permanent teeth diagnosed with vital or non-vital pulps and need nonsurgical root canal treatment.
Key exclusion criteria (1 listed)
- 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.
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| protaper nextAlso: Edge-one firerotary systems used on patients need root canal treatment | Behavioural | Single visit, multiple visit |
Primary outcome
Visual analogue scale
Time frame: 24 months
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
1 secondary outcome
Verbal analogue scale
Time frame: 24 moths
Results and safety
Results are not available in the source record.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 3 Mar 2021.
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Yahia Alyami contact
1 site in 1 country: see every site and its status.
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.