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Effect of long acting anesthetic on pain during and after root canal treatment

Effect of long acting supplementary local anesthetic on intra and post operative pain in single visit root canal treatment – a randomised control trail - NIL

Status
Active, not recruiting
Phases
Phase 3Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2023/11/060116
Enrollment
60
Registered
2023-11-22
Start date
Unknown
Completion date
Unknown
Last updated
2023-12-19

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

Conditions

Health Condition 1: K044- Acute apical periodontitis of pulpal origin

Interventions

Intervention1: Ropin: 0.5% Ropivacaine for a duration of 48 hours Control Intervention1: Lignox A: 2% Lignocaine 1:80,000 epinephrine for a duration of 48 hours

Sponsors

Dr Apeksha Rao
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients who require endodontic treatment in Single rooted pre molar teeth with a clinical diagnosis of symptomatic irreversible pulpitis or symptomatic apical periodontitis Patients giving history of spontaneous, continuous, lingering, gnawing or throbbing type of pain with a VAS score > 6. On cold vitality testing, eliciting response of lingering pain, delayed or negative response Only one teeth involved in the quadrant Teeth without anatomic variations, for example, receded pulp chamber, calcified canals, or sharply curved canals Patients not on analgesics or sedative medications 24-48hrs before root canal therapy

Exclusion criteria

Exclusion criteria: Patients with known allergy to anaesthetics Asymptomatic irreversible pulpitis and other pulpal or periodontal disease diagnosis Patients who are diabetic, pregnant or any other systemic illness Retreatment

Design outcomes

Primary

MeasureTime frame
intra operative and post operative pain assessment using VAS scaleTimepoint: 2,6,12,24,48 hours

Secondary

MeasureTime frame
intro operative and post operative pain assessment difference in age and gender using VAS scale and use of post operative analgesicTimepoint: 2,6,12,24,48 hours

Countries

India

Contacts

Public ContactApeksha Rao

Vokkaligara Sangha Dental College and Hospital

anithamanasi18@gmail.com9845919324

Outcome results

None listed

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