A clinical trail to evaluate the pain after root canal treatment by two diiferent rotary systems

EVALUATION OF POST OPERATIVE PAIN IN SINGLE VISIT ROOT CANAL TREATMENT WITH PROTAPER NEXT AND M TWO ROTARY SYSTEMS IN ASYMPTOMATIC IRREVERSIBLE PULPITIS OF MULTIROOTED TEETH-A RANDOMIZED CLINICAL TRIAL. - EPSRT

Status

Active, not recruiting

Phases

Phase 4

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2017/02/007774

Enrollment

Registered

2017-02-03

Start date

Unknown

Completion date

Unknown

Last updated

2021-11-24

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

Conditions

Health Condition 1: null- Asymptomatic irreversible pulpitis

Interventions

Intervention1: Protaper Next rotary file: a newly developed rotary file for efficient cleanig and shaping of root canals Control Intervention1: Mtwo rotary file: A new rotary file system developed to

Eligibility

Inclusion criteria

Inclusion criteria: 1.Multi rooted teeth with asymptomatic irreversible pulpitis with normal periapical radiographic appearance and periapical radiolucency less than 2mm will be scheduled for initial endodontic treatment. 2.Patients of age group between 18-50 3.Subjects who will show prolonged response even after the removal of the stimulus. Patient who has the ability to understand the use of pain scales will be provided informed consent for endodontic treatment.

Exclusion criteria

Exclusion criteria: 1.Patients with sinus tract, periapical abscess or facial cellulitis. 2.Patient with known allergies, or any contraindication to opioid or non-opioid analgesics including aspirin or NSAIDs. Patients with known allergy to local anaesthesia, sodium hypochlorite and chlorhexidine. Presence of systemic diseases like cardiovascular disease, renal disease, and any bleeding disorders or anti coagulant use with in last month. 3.Pregnants and lactating mothers. 4.Patients under pain medication for any other illness. 5. Patients who are unable or unwilling to complete the pain questionnaires; 6. Patients who are unwilling to sign consent for endodontic treatment

Design outcomes

Primary

Measure	Time frame
post treatment pain evalution using visual analog scale after 8hours,12 hours,24hours,48hours,72hoursTimepoint: post treatment pain evalution using visual analog scale 8hours,12 hours,24hours,48hours,72hours	—

Secondary

Measure	Time frame
post treatment pain evalution using visual analog scaleTimepoint: pain evaluation 24, 48, 72 hours after treatment	—

Countries

India

Contacts

Public ContactDrSuneel kumar C

Narayana dental college and hospital

drmadhuk15@gmail.com9391046354

Outcome results

None listed

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