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The Incidence of Postoperative Pain After Using Different Types of Sealers

Primary Purpose

Post Operative Pain, Root Canal Sealers, Sillicon Based Sealers

Status
Not yet recruiting
Phase
Not Applicable
Locations
Egypt
Study Type
Interventional
Intervention
Primary local anesthesia
Supplemental local anesthesia
Removal Of Caries and Access Cavity
Rubber dam isolation of tooth
Bleeding control
Canal negotiation
Coronal flaring
Working Length Determination (W.L)
Glide path
Irrigation
Cleaning and shaping using rotary system
Second w.l determination
Apical gauging
Activation of the irrigant
Master cone check
application of resin based sealer inside the canal in the resin based sealer group
application of the sillicon based sealer inside the canal in the sillicon based group
Obturation
Visual Analogue Scale (VAS)
Sponsored by
British University In Egypt
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional screening trial for Post Operative Pain

Eligibility Criteria

18 Years - 50 Years (Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria: • Patient's age ranges from 18-50 years old. Patients with teeth diagnosed with symptomatic irreversible pulpitis. Normal periapical condition confirmed by normal periapical radiograph The teeth are restorable Teeth are periodontally free, with no mobility and negative to percussion and palpation test. Exclusion Criteria: • Teeth with immature roots Non restorable teeth Medically compromised patients with systemic complication that would alter the treatment. Necrotic teeth Teeth with apical periodontitis or periapical lesions Teeth that need multiple visits treatment like necrotic cases.

Sites / Locations

  • British University in Egypt

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Experimental

Arm Label

Group (1) Resin Based Sealer intervention

Group (2) Silicone Based Sealer intervention

Arm Description

evaluate the incidence and intensity of post-operative pain after obturation using resin based sealers.

evaluate the incidence and intensity of post-operative pain after obturation using sillicon based sealers.

Outcomes

Primary Outcome Measures

Postoperative pain
Pain is evaluated using visual analogue scale (VAS) which is a pain rating scale. Scores are based on measures that are self-reported of symptoms that are recorded through a single handwritten mark placed at one point along the length of a 10-cm line representing a continuum between the two ends of the scale; on the left end of the scale (0 cm) means "no pain" and the on the right end of the scale (10 cm) "worst pain" Each Outcome Measure should typically only specify a single time point of assessment
Postoperative pain
Pain is evaluated using visual analogue scale (VAS) which is a pain rating scale. Scores are based on measures that are self-reported of symptoms that are recorded through a single handwritten mark placed at one point along the length of a 10-cm line representing a continuum between the two ends of the scale; on the left end of the scale (0 cm) means "no pain" and the on the right end of the scale (10 cm) "worst pain"
Postoperative pain
Pain is evaluated using visual analogue scale (VAS) which is a pain rating scale. Scores are based on measures that are self-reported of symptoms that are recorded through a single handwritten mark placed at one point along the length of a 10-cm line representing a continuum between the two ends of the scale; on the left end of the scale (0 cm) means "no pain" and the on the right end of the scale (10 cm) "worst pain"
Postoperative pain
Pain is evaluated using visual analogue scale (VAS) which is a pain rating scale. Scores are based on measures that are self-reported of symptoms that are recorded through a single handwritten mark placed at one point along the length of a 10-cm line representing a continuum between the two ends of the scale; on the left end of the scale (0 cm) means "no pain" and the on the right end of the scale (10 cm) "worst pain"
Postoperative pain
Pain is evaluated using visual analogue scale (VAS) which is a pain rating scale. Scores are based on measures that are self-reported of symptoms that are recorded through a single handwritten mark placed at one point along the length of a 10-cm line representing a continuum between the two ends of the scale; on the left end of the scale (0 cm) means "no pain" and the on the right end of the scale (10 cm) "worst pain"

Secondary Outcome Measures

Full Information

First Posted
December 16, 2022
Last Updated
April 22, 2023
Sponsor
British University In Egypt
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1. Study Identification

Unique Protocol Identification Number
NCT05841290
Brief Title
The Incidence of Postoperative Pain After Using Different Types of Sealers
Official Title
The Incidence of Postoperative Pain After Using Different Types of Sealers (A Randomized Clinical Trial)
Study Type
Interventional

2. Study Status

Record Verification Date
April 2023
Overall Recruitment Status
Not yet recruiting
Study Start Date
May 2023 (Anticipated)
Primary Completion Date
December 2023 (Anticipated)
Study Completion Date
December 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
British University In Egypt

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No

5. Study Description

Brief Summary
The aim of this randomized clinical trial is to evaluate and compare the incidence and intensity of post-operative pain after obturation using resin and silicon-based sealers.
Detailed Description
The main objectives of root canal therapy are to achieve long-term comfort, function, and aesthetics for the patients and prevention of reinfection of tooth. These objectives are provided through complete cleaning, shaping, and obturation of canals of affected teeth . Some patients may report moderate-to-severe pain and/or swelling following root canal treatment . This is detrimental for both patient and dentist and may entail an unscheduled emergency visit by patients to relieve their symptoms. Postoperative pain is considered a clinical outcome that exhibits the multifactorial nature of patients' responses to variables among treatment procedures such as maintaining the working length to the apical constriction, finishing the endodontic treatment in single visit or multiple visit, instrumentation technique and the type of endodontic sealer used for obturation . Such pain occurrence is mainly due to mechanical, chemical or microbial injury to the periapical tissues . Trauma of periapical tissue or bacterial extrusion and root canal sealer specifically, extrusion of root canal sealer can disrupt periodontal tissues and cause inflammatory reactions. The intensity of this reaction depends on the composition of the sealer . Root canal sealers can play a crucial role in this regard by coming in contact with the periapical tissues through apical foramen and lateral canals causing a localized inflammation with a direct influence on the degree of inflammation based on the composition of the sealer in turn influencing postoperative pain levels . Silicone is inert and biocompatible and has been widely used in medicine as an implant material Silicone-based root-canal sealers are also available. However, there are no data on the clinical performance of this type of material in endodontic treatment .

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Post Operative Pain, Root Canal Sealers, Sillicon Based Sealers, Resin Based Sealers

7. Study Design

Primary Purpose
Screening
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Root Canal Treatment (RCT) with 2 parallel groups, two arms, superiority trial with 1:1 allocation ratio
Masking
None (Open Label)
Allocation
Randomized
Enrollment
40 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Group (1) Resin Based Sealer intervention
Arm Type
Experimental
Arm Description
evaluate the incidence and intensity of post-operative pain after obturation using resin based sealers.
Arm Title
Group (2) Silicone Based Sealer intervention
Arm Type
Experimental
Arm Description
evaluate the incidence and intensity of post-operative pain after obturation using sillicon based sealers.
Intervention Type
Procedure
Intervention Name(s)
Primary local anesthesia
Intervention Description
Tooth will be anaesthetized using Local anesthesia containing Articaine with epinephrine 1:100,000.
Intervention Type
Procedure
Intervention Name(s)
Supplemental local anesthesia
Other Intervention Name(s)
intraligamentary injection / Intrapulpal Anesthesia
Intervention Description
if needed
Intervention Type
Procedure
Intervention Name(s)
Removal Of Caries and Access Cavity
Intervention Description
• Access cavity will be performed using a carbide round steel bur and tapered diamond stone until complete deroofing.
Intervention Type
Procedure
Intervention Name(s)
Rubber dam isolation of tooth
Intervention Description
Rubber dam isolation of tooth using certain clamps .
Intervention Type
Procedure
Intervention Name(s)
Bleeding control
Intervention Description
bleeding is controlled by using excavator for the removing the pulp tissue . using a piece of cotton soaked with Sodium hypochlorite. using local anesthesia with vasoconstrictor if needed and if suitable for the patient.
Intervention Type
Procedure
Intervention Name(s)
Canal negotiation
Other Intervention Name(s)
Coronal patency, Apical patency
Intervention Description
Coronal patency of the coronal and the Middle part of the canal using file #10 Apical patency of the apical part of the canal using #10
Intervention Type
Procedure
Intervention Name(s)
Coronal flaring
Intervention Description
Coronal flaring using Orifice opener of a certain Rotary system in and out motion first then brushing motion touching all the canal walls
Intervention Type
Procedure
Intervention Name(s)
Working Length Determination (W.L)
Intervention Description
Working length determination (W.L) using #10 K File , working length is recorded using apex locator and confirmatory radiograph.
Intervention Type
Procedure
Intervention Name(s)
Glide path
Intervention Description
Glide path of the canal Using #10 ,15 ,20 ,25 K files till becoming Super-Loose Inside the Canal at the recorded w.l to create a path for the rotary file .
Intervention Type
Procedure
Intervention Name(s)
Irrigation
Intervention Description
Irrigation using 5.25% sodium hypochlorite introduced using side vented needle
Intervention Type
Procedure
Intervention Name(s)
Cleaning and shaping using rotary system
Intervention Description
Cleaning and shaping using rotary system plus irrigation and apical patency between every rotary file .
Intervention Type
Procedure
Intervention Name(s)
Second w.l determination
Intervention Description
Second w.l determination using electronic apex locator before using final finishing rotary file .
Intervention Type
Procedure
Intervention Name(s)
Apical gauging
Intervention Description
Establish the depth of apical constriction - this is the zero reading on your apex locator. your working length will be 0.5mm - 1mm short of this. After cleaning and preparing the canal system to your working length, passively insert 02 taper hand files, starting from #15. If the file goes past the apical constriction (your working length + 0.5-1mm), then choose the next largest file and repeat. When a file passively binds short of the apical constriction, that will be the upper limit of the apical constriction diameter. The smaller file before that would be the lower limit. Apical gauging helps with: Choosing the best master cone that closely matches canal length and taper Achieving true tug back - as opposed to false tug back! Minimising gutta percha extrusions during obturation
Intervention Type
Procedure
Intervention Name(s)
Activation of the irrigant
Intervention Description
Activation of the irrigant using Manual Dynamic Agitation and Ultra x or eddy tips for activation
Intervention Type
Procedure
Intervention Name(s)
Master cone check
Intervention Description
Master cone check Clinically and confirmatory radiograph
Intervention Type
Drug
Intervention Name(s)
application of resin based sealer inside the canal in the resin based sealer group
Other Intervention Name(s)
AH plus
Intervention Description
application done by inserting inside the canal by spreader or master cone
Intervention Type
Diagnostic Test
Intervention Name(s)
application of the sillicon based sealer inside the canal in the sillicon based group
Other Intervention Name(s)
Gutta flow 2
Intervention Description
application done by injection inside the canal
Intervention Type
Procedure
Intervention Name(s)
Obturation
Intervention Description
done by lateral condensation technique
Intervention Type
Diagnostic Test
Intervention Name(s)
Visual Analogue Scale (VAS)
Intervention Description
Pain is evaluated using visual analogue scale (VAS) which is a pain rating scale. Scores are based on measures that are self-reported of symptoms that are recorded through a single handwritten mark placed at one point along the length of a 10-cm line representing a continuum between the two ends of the scale; on the left end of the scale (0 cm) means "no pain" and the on the right end of the scale (10 cm) "worst pain"
Primary Outcome Measure Information:
Title
Postoperative pain
Description
Pain is evaluated using visual analogue scale (VAS) which is a pain rating scale. Scores are based on measures that are self-reported of symptoms that are recorded through a single handwritten mark placed at one point along the length of a 10-cm line representing a continuum between the two ends of the scale; on the left end of the scale (0 cm) means "no pain" and the on the right end of the scale (10 cm) "worst pain" Each Outcome Measure should typically only specify a single time point of assessment
Time Frame
after 6 hours of endodontic treatment
Title
Postoperative pain
Description
Pain is evaluated using visual analogue scale (VAS) which is a pain rating scale. Scores are based on measures that are self-reported of symptoms that are recorded through a single handwritten mark placed at one point along the length of a 10-cm line representing a continuum between the two ends of the scale; on the left end of the scale (0 cm) means "no pain" and the on the right end of the scale (10 cm) "worst pain"
Time Frame
after 12 hours of endodontic treatment
Title
Postoperative pain
Description
Pain is evaluated using visual analogue scale (VAS) which is a pain rating scale. Scores are based on measures that are self-reported of symptoms that are recorded through a single handwritten mark placed at one point along the length of a 10-cm line representing a continuum between the two ends of the scale; on the left end of the scale (0 cm) means "no pain" and the on the right end of the scale (10 cm) "worst pain"
Time Frame
after 24 hours of endodontic treatment
Title
Postoperative pain
Description
Pain is evaluated using visual analogue scale (VAS) which is a pain rating scale. Scores are based on measures that are self-reported of symptoms that are recorded through a single handwritten mark placed at one point along the length of a 10-cm line representing a continuum between the two ends of the scale; on the left end of the scale (0 cm) means "no pain" and the on the right end of the scale (10 cm) "worst pain"
Time Frame
after 48 hours of endodontic treatment
Title
Postoperative pain
Description
Pain is evaluated using visual analogue scale (VAS) which is a pain rating scale. Scores are based on measures that are self-reported of symptoms that are recorded through a single handwritten mark placed at one point along the length of a 10-cm line representing a continuum between the two ends of the scale; on the left end of the scale (0 cm) means "no pain" and the on the right end of the scale (10 cm) "worst pain"
Time Frame
after 72 hours of endodontic treatment
Other Pre-specified Outcome Measures:
Title
sealer extrusion
Description
The 2 blinded and calibrated examiners will evaluate the immediate periapical radiographs after canal obturation. Sealer extrusion will classified to either absent or present. If there will be a sealer extrusion in at least 1 root for multirooted teeth, will be regarded as the "presence" of sealer extrusion Measured by clinical symptoms and signs ( pain , swelling , parasthesia )
Time Frame
average 1 week
Title
root-filling voids
Description
The 2 blinded and calibrated examiners will evaluate the immediate periapical radiographs after canal obturation. will classified to either absent or present. If there will be root-filling voids in at least 1 root for multirooted teeth, will be regarded as the "presence" of it
Time Frame
after obturation is done intra-appointment
Title
the level of root filling
Description
The 2 blinded and calibrated examiners will evaluate the immediate periapical radiographs after canal obturation. just discovered it will be corrected
Time Frame
after obturation is done intra-appointment

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
50 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: • Patient's age ranges from 18-50 years old. Patients with teeth diagnosed with symptomatic irreversible pulpitis. Normal periapical condition confirmed by normal periapical radiograph The teeth are restorable Teeth are periodontally free, with no mobility and negative to percussion and palpation test. Exclusion Criteria: • Teeth with immature roots Non restorable teeth Medically compromised patients with systemic complication that would alter the treatment. Necrotic teeth Teeth with apical periodontitis or periapical lesions Teeth that need multiple visits treatment like necrotic cases.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Kareem Mohammed Elhoseny, Bachelor
Phone
01157215056
Email
Kareem.Darwish@bue.edu.eg
First Name & Middle Initial & Last Name or Official Title & Degree
Engy Medhat Kataia, professor at BUE
Phone
01001859898
Email
Engy.medhat@bue.edu.eg
Facility Information:
Facility Name
British University in Egypt
City
El Shorouk
State/Province
Cairo
ZIP/Postal Code
+20 19283
Country
Egypt

12. IPD Sharing Statement

Citations:
PubMed Identifier
26778004
Citation
Torabinejad M, White SN. Endodontic treatment options after unsuccessful initial root canal treatment: Alternatives to single-tooth implants. J Am Dent Assoc. 2016 Mar;147(3):214-20. doi: 10.1016/j.adaj.2015.11.017. Epub 2016 Jan 9.
Results Reference
background
PubMed Identifier
33344681
Citation
Javidi M, Zarei M, Ashrafpour E, Gharechahi M, Bagheri H. Post-treatment Flare-up Incidence after Using Nano Zinc Oxide Eugenol Sealer in Mandibular First Molars with Irreversible Pulpitis. J Dent (Shiraz). 2020 Dec;21(4):307-313. doi: 10.30476/DENTJODS.2020.83231.1041.
Results Reference
background
PubMed Identifier
31435267
Citation
AlRahabi MK. Predictors, prevention, and management of postoperative pain associated with nonsurgical root canal treatment: A systematic review. J Taibah Univ Med Sci. 2017 May 9;12(5):376-384. doi: 10.1016/j.jtumed.2017.03.004. eCollection 2017 Oct.
Results Reference
background
PubMed Identifier
3471726
Citation
Genet JM, Hart AA, Wesselink PR, Thoden van Velzen SK. Preoperative and operative factors associated with pain after the first endodontic visit. Int Endod J. 1987 Mar;20(2):53-64. doi: 10.1111/j.1365-2591.1987.tb00590.x. No abstract available.
Results Reference
background
PubMed Identifier
24688584
Citation
Christian Gomes Moura C, Cristina Cunha T, Oliveira Crema V, Dechichi P, Carlos Gabrielli Biffi J. A study on biocompatibility of three endodontic sealers: intensity and duration of tissue irritation. Iran Endod J. 2014 Spring;9(2):137-43. Epub 2014 Mar 8.
Results Reference
background
PubMed Identifier
26632225
Citation
Zhang W, Peng B. Tissue reactions after subcutaneous and intraosseous implantation of iRoot SP, MTA and AH Plus. Dent Mater J. 2015;34(6):774-80. doi: 10.4012/dmj.2014-271.
Results Reference
background
PubMed Identifier
6375634
Citation
Habal MB. The biologic basis for the clinical application of the silicones. A correlate to their biocompatibility. Arch Surg. 1984 Jul;119(7):843-8. doi: 10.1001/archsurg.1984.01390190081019.
Results Reference
background
PubMed Identifier
8545137
Citation
Marcus DA. Interrelationships of neurochemicals, estrogen, and recurring headache. Pain. 1995 Aug;62(2):129-139. doi: 10.1016/0304-3959(95)00052-T.
Results Reference
background
PubMed Identifier
9627895
Citation
Dao TT, Knight K, Ton-That V. Modulation of myofascial pain by the reproductive hormones: a preliminary report. J Prosthet Dent. 1998 Jun;79(6):663-70. doi: 10.1016/s0022-3913(98)70073-3.
Results Reference
background
PubMed Identifier
1402571
Citation
Walton R, Fouad A. Endodontic interappointment flare-ups: a prospective study of incidence and related factors. J Endod. 1992 Apr;18(4):172-7. doi: 10.1016/S0099-2399(06)81413-5.
Results Reference
background
PubMed Identifier
18352900
Citation
Mehrvarzfar P, Shababi B, Sayyad R, Fallahdoost A, Kheradpir K. Effect of supraperiosteal injection of dexamethasone on postoperative pain. Aust Endod J. 2008 Apr;34(1):25-9. doi: 10.1111/j.1747-4477.2007.00076.x.
Results Reference
background
PubMed Identifier
23633809
Citation
Ali SG, Mulay S, Palekar A, Sejpal D, Joshi A, Gufran H. Prevalence of and factors affecting post-obturation pain following single visit root canal treatment in Indian population: A prospective, randomized clinical trial. Contemp Clin Dent. 2012 Oct;3(4):459-63. doi: 10.4103/0976-237X.107440.
Results Reference
background
PubMed Identifier
11811742
Citation
Watkins CA, Logan HL, Kirchner HL. Anticipated and experienced pain associated with endodontic therapy. J Am Dent Assoc. 2002 Jan;133(1):45-54. doi: 10.14219/jada.archive.2002.0020.
Results Reference
background
PubMed Identifier
16934622
Citation
Cleghorn BM, Christie WH, Dong CC. Root and root canal morphology of the human permanent maxillary first molar: a literature review. J Endod. 2006 Sep;32(9):813-21. doi: 10.1016/j.joen.2006.04.014. Epub 2006 Jun 30.
Results Reference
background
PubMed Identifier
15273637
Citation
Claffey E, Reader A, Nusstein J, Beck M, Weaver J. Anesthetic efficacy of articaine for inferior alveolar nerve blocks in patients with irreversible pulpitis. J Endod. 2004 Aug;30(8):568-71. doi: 10.1097/01.don.0000125317.21892.8f.
Results Reference
background
PubMed Identifier
15793381
Citation
Mikesell P, Nusstein J, Reader A, Beck M, Weaver J. A comparison of articaine and lidocaine for inferior alveolar nerve blocks. J Endod. 2005 Apr;31(4):265-70. doi: 10.1097/01.don.0000140576.36513.cb.
Results Reference
background
PubMed Identifier
18771838
Citation
Risso PA, Cunha AJ, Araujo MC, Luiz RR. Postobturation pain and associated factors in adolescent patients undergoing one- and two-visit root canal treatment. J Dent. 2008 Nov;36(11):928-34. doi: 10.1016/j.jdent.2008.07.006. Epub 2008 Sep 3.
Results Reference
background
PubMed Identifier
11471639
Citation
Menke ER, Jackson CR, Bagby MD, Tracy TS. The effectiveness of prophylactic etodolac on postendodontic pain. J Endod. 2000 Dec;26(12):712-5. doi: 10.1097/00004770-200012000-00010.
Results Reference
background
PubMed Identifier
15910469
Citation
Sathorn C, Parashos P, Messer HH. Effectiveness of single- versus multiple-visit endodontic treatment of teeth with apical periodontitis: a systematic review and meta-analysis. Int Endod J. 2005 Jun;38(6):347-55. doi: 10.1111/j.1365-2591.2005.00955.x.
Results Reference
background
PubMed Identifier
11402269
Citation
Spangberg LS. Evidence-based endodontics: the one-visit treatment idea. Oral Surg Oral Med Oral Pathol Oral Radiol Endod. 2001 Jun;91(6):617-8. doi: 10.1067/moe.2001.116720. No abstract available.
Results Reference
background
PubMed Identifier
7561660
Citation
al-Omari MA, Dummer PM. Canal blockage and debris extrusion with eight preparation techniques. J Endod. 1995 Mar;21(3):154-8. doi: 10.1016/s0099-2399(06)80443-7.
Results Reference
background
PubMed Identifier
15611742
Citation
Carrotte P. Endodontics: Part 7. Preparing the root canal. Br Dent J. 2004 Nov 27;197(10):603-13. doi: 10.1038/sj.bdj.4811823.
Results Reference
background
PubMed Identifier
15186245
Citation
Ng YL, Glennon JP, Setchell DJ, Gulabivala K. Prevalence of and factors affecting post-obturation pain in patients undergoing root canal treatment. Int Endod J. 2004 Jun;37(6):381-91. doi: 10.1111/j.1365-2591.2004.00820.x.
Results Reference
background
PubMed Identifier
31794999
Citation
Fonseca B, Coelho MS, Bueno CEDS, Fontana CE, Martin AS, Rocha DGP. Assessment of Extrusion and Postoperative Pain of a Bioceramic and Resin-Based Root Canal Sealer. Eur J Dent. 2019 Jul;13(3):343-348. doi: 10.1055/s-0039-3399457. Epub 2019 Dec 3.
Results Reference
background
PubMed Identifier
34069521
Citation
Shim K, Jang YE, Kim Y. Comparison of the Effects of a Bioceramic and Conventional Resin-Based Sealers on Postoperative Pain after Nonsurgical Root Canal Treatment: A Randomized Controlled Clinical Study. Materials (Basel). 2021 May 19;14(10):2661. doi: 10.3390/ma14102661.
Results Reference
background
Citation
Chitra Sachdev Comparative Evaluation of Post-Operative Pain On Unintentional Extruded Three Different Root Canal Sealers Periapically- An Invivo Study. Int J Recent Sci Res. 12(03), pp. 41232-234.
Results Reference
background
PubMed Identifier
35173897
Citation
Khandelwal A, Jose J, Teja KV, Palanivelu A. Comparative evaluation of postoperative pain and periapical healing after root canal treatment using three different base endodontic sealers - A randomized control clinical trial. J Clin Exp Dent. 2022 Feb 1;14(2):e144-e152. doi: 10.4317/jced.59034. eCollection 2022 Feb.
Results Reference
background
PubMed Identifier
17415063
Citation
Alexander I. Electronic medical records for the orthopaedic practice. Clin Orthop Relat Res. 2007 Apr;457:114-9. doi: 10.1097/BLO.0b013e3180342802.
Results Reference
background

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The Incidence of Postoperative Pain After Using Different Types of Sealers

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