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Comparison of Manual and Rotary Instrumentation Techniques on Postoperative Pain

Comparison of the Effects of Manual and Rotary Instrumentation Techniques on Postoperative Pain in Mandibular Molar Teeth with Asymptomatic Irreversible Pulpitis: A Prospective Randomized Clinical Trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2015041521780N1
Enrollment
96
Registered
2015-05-23
Start date
2015-03-06
Completion date
Unknown
Last updated
2018-02-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Postoperative Pain. XVIIIInjury, poisoning and certain other consequences of external causes XX External causes of morbidity and mortality XXI Factors influencing health status and contact with health services

Interventions

Intervention 1: First intervention group: Instrumentation and treatment of mandibular first and second molar canals with rotary RaCe system by 7 RaCe rotary files and crowndown technique according
Treatment - Surgery
First intervention group: Instrumentation and treatment of mandibular first and second molar canals with rotary RaCe system by 7 RaCe rotary files and crowndown technique according to manufacturers
Second intervention group:Treatment and instrumentation of mandibular first and second molars canals with manual k-flexofiles and k-files by stepback technique in one visit.

Sponsors

Vice Chancellor Research of Dental Faculty of Tabriz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: Inclusion Criteria: Age over than 18 years old ; With pulpal status of asymptomatic irreversible pulpitis ; Normal periradicular status radio graphically ; Systemically healthy ; Conducive to restoration ; Needing selective one-visit treatment ; Presence of lip sign after administration of anesthesia ; Presence of bleeding after exposure of the pulp ; Teeth with 3 or 4 root canals ; No drug use or use of 400 mg of ibuprofen during the 24-hour postoperative interval ; Straight with not difficult to access SLA. Exclusion Criteria: Age Under than 18 years old ; Healthy pulpal status or reversible pulpitis or symptomatic irreversible pulpitis or necrosis ; Widening of PDL or radiolucency or radiopacity in the origin of periradicular ; Systemic disease ; Breast-feeding ; Pregnancy ; Hypersensitivity to lidocaine ; Impossible to restore the teeth ; Presence of a crown before the procedure ; Needing 2-visit treatment or any extra procedure such as incision and drainage ; Absence of lip sign after administration of anesthesia ; Absence of bleeding after exposure of the pulp ; Teeth with 1 or 2 root canals ; The presence of a difficult root canal anatomy (root canals with extreme curvatures (over 30°) and C-shape canals) ; Internal or external resorption ; Teeth with open apices ; Radiographically untraceable canal path or any accident or complication occurring during treatment (calcified canals, inability to achieve apical patency in any canal) ; Use of analgesics 12 hours before treatment ; Use more than 400 mg of ibuprofen during the 24-hour postoperative interval or any dose after 24 hours ; Severe labial or lingual malpositioning of teeth making it difficult to access SLA ; More teeth needing RCT on the same side.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Postoperative Pain. Timepoint: 4,8,12,24,48 hour and one week intervals. Method of measurement: Use of Visual Analog Scale(VAS) picture.

Secondary

MeasureTime frame
Use of Analgestic Drugs (ibuprofen 400 mg). Timepoint: In first 24 hours until one week(use or not use of analgestic drugs in first 24 hours until one week). Method of measurement: Ask the pationts.;The number of painless pationts. Timepoint: 4,8,12,24,48 hours and one week intervals. Method of measurement: Use of Visual Analog Scale(VAS) picture.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactSaied Rahimi

Endodontic Department of Faculty of Dentistry of Tabriz University of Medical Sciences

rahimis@tbzmed.ac.ir ; talebzadeh.g@gmail.com ; nima_talebzade@yahoo.com+98 41 3544 6872

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026