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Effect of rotary file systems and irrigation agitation techniques on post-operative pain after endodontic therapy in patients with symptomatic irreversible pulpitis teeth.

The effect of novel rotary file systems along with irrigation agitation technique on postoperative pain in teeth with symptomatic irreversible pulpitis : a randomized clinical trail

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2021/04/032814
Enrollment
80
Registered
2021-04-13
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: Z658- Other specified problems related to psychosocial circumstances

Interventions

Intervention1: Trunatomy file system along with Manual dynamic irrigation agitation: Instrumentation with Trunatomy rotary file system(endodontic rotary file system) along with manual dynamic agitatio

Sponsors

Dr Ravuri Varshini Meghana
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients with symptomatic irreversible pulpitis in posterior teeth. Healthy patients of age group between 18-50 yrs. Patients with preoperative pain scores which will vary from moderate to severe pain on a visual analog scale(VAS). Patients who will have the ability to understand and to use the pain scale

Exclusion criteria

Exclusion criteria: Patients with pain on percussion Patients with traumatic occlusion, severe malocclusion Teeth with calcified canals Teeth with periapical radiolucency Teeth with root resorption Teeth with immature open apex Patients with Re -RCT will be excluded. • Patients who has taken analgesic or anti-inflammatory drugs within the last 12 hour • Patients with known allergy to local anesthesia, sodium hypochlorite and chlorhexidine. Presence of systemic diseases like cardiovascular disease, renal disease, bleeding disorders or any anti-coagulant use with in last month. Pregnant and lactating mothers. Patients who are unable or unwilling to complete the pain questionnaires. Patients who are unwilling to sign consent for endodontic treatment

Design outcomes

Primary

MeasureTime frame
Assessment of post-operative Pain scores using Visual Analog ScaleTimepoint: at 6,24,48,and 72 hours and on 7th day

Secondary

MeasureTime frame
assessing quality of life using OHIP 14 criteriaTimepoint: at 72 hours

Countries

India

Contacts

Public ContactDr Lavanya

Narayana Dental College and Hospital

govulakiranmayi24@gmail.com9440932608

Outcome results

None listed

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