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Comparison of the postoperative pain after root canal therapy(in asymptomatic patients) with two different preparation methods (A randomized clinical study)

Comparison of the postoperative pain after root canal therapy(in asymptomatic patients) with two different preparation methods (A randomized clinical study)

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2013071313970N1
Enrollment
42
Registered
2014-03-07
Start date
2013-12-20
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

Condition 1: Asymptomatic Necrosis of the pulp. Condition 2: Asymptomatic irreversible pulpitis. Asymptomatic Necrosis of the pulp Asymptomatic irreversible pulpitis

Interventions

Intervention 1: Root canals prepared by Wave one technique. Intervention 2: Root canals prepared by Rotary Protaper technique.
Treatment - Other
Root canals prepared by Wave one technique
Root canals prepared by Rotary Protaper technique

Sponsors

Tehran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
15 Years to 55 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria:Patient age 15-55; One or multi roots teeth with closed apex (molar and premolar ); Teeth with asymptomatic irreversible pulpitis or asymptomatic necrosis; Intermediate root curvature Exclusion criteria: Using any medicine before treatment(antibiotic and analgesics); Internal and external resorption which can be seen in radiography; Trismus; Sinus tract; Internal Ankylosis; Retreatment; Systemic disease or constant use of any medicine; Not filling the consent form; Trauma history; Pregnancy; Not being in occlusion ; Addiction to any drug; Lack of patient compliance in using the medicine accurately on time; Not obeying the usage protocol by patient or not trusting his/her; Not being able to use NSAID(because of side effects )before treatment or after using

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Post operative pain. Timepoint: 0-6-12-18-24-48-72. Method of measurement: VAS.

Secondary

MeasureTime frame
Analgesics consumption. Timepoint: 0-6-2-18-24-48-72. Method of measurement: Number of Analgesic consumption.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr.Mohammd Saeed Sheykh Rezaee

School of Dentistry, Tehran University of Medical Sciences

sheykh_r@yahoo.com+98 21 8849 7389

Outcome results

None listed

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