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Assessment of postoperative pain after using two root canal sealers along with irrigating needles in symptomatic irreversible pulpitis mandibular molars - A clinical trial

Evaluation and comparison of bio-ceramic and resin based sealer along with two types of irrigating needles on post operative pain and quality of life in mandibular molar teeth with symptomatic irreversible pulpitis – A randomized clinical trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2023/05/053313
Enrollment
60
Registered
2023-05-31
Start date
Unknown
Completion date
Unknown
Last updated
2024-01-22

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

Conditions

Health Condition 1: K040- Pulpitis

Interventions

Intervention1: Bio-ceramic root canal sealer: Bio-ceramic materials can be classified as bioinert,bioactive or biodegradable according to the interaction with surrounding tissues and this material wil

Sponsors

YASMEEN MOHAMMED AZEEM
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: a.Patients with symptomatic irreversible pulpitis (mandibular molar). b.Healthy patients of age group between 18-55 yrs. c.Patients with preoperative pain scores which will vary from moderate to severe pain on a visual analog scale (VAS). d.Patients who will have the ability to understand and to use the pain scale.

Exclusion criteria

Exclusion criteria: •Patients with any uncontrolled systemic diseases. •Retreatments of root canals. •Teeth with immatureopen apex. •Patients who initiated root canal treatment in other clinics. •Patients who has taken analgesic or anti-inflammatory drugs within the last 12 hours. •Patients with known allergy to local anaesthesia, sodium hypochlorite and chlorhexidine. •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
post operative pain evaluation using visual analogue scale.Timepoint: 6, 24, 48, 72 hours and on 7th day after the endodontic treatment—

Secondary

MeasureTime frame
quality of life assessmentTimepoint: 7th day after root canal treatment—

Countries

India

Contacts

Public ContactYasmeen Mohammed Azeem

Narayana Dental College And Hospital, Nellore

govulakiranmayi24@gmail.com9440932608

Outcome results

None listed

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