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a clinical study of cold application after main block using 4% articaine in acute dental pain of mandibular molar teeth.

Efficacy of Endo-Ice intrapulpal application after inferior alveolar nerve block and articaine buccal infiltration in patients with symptomatic irreversible pulpitis of mandibular molarsâ??a randomized placebo controlled trial.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2021/10/037571
Enrollment
60
Registered
2021-10-26
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: R52- Pain, unspecified Health Condition 2: K040- Pulpitis

Interventions

Intervention1: endo ice: lignocaine (2%) adrenaline (1:80000)+buccal infiltration with articaine (4%) with adrenaline (1:100000) and intra-pulpal cold application with endo ice. Control Intervention1:

Sponsors

Dr Umesh Kumar
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: The inclusion criteria for the study were as follows: moderate to severe pain in the mandibular first molar, a prolonged response to cold testing with an ice stick and an electric pulp tester (Kerr Pulp Tester; Analytic Technology Corp, Redmond, WA), the absence of any periapical radiolucency on radiographs except for a widened periodontal ligament, a vital coronal pulp on access opening, and the ability of the subject to understand the use of pain scales. The subjects were in good health, and none were taking any medication that would alter pain perception, as determined by oral questioning and a written questionnaire.

Exclusion criteria

Exclusion criteria: The exclusion criteria for the study were as follows: subjects younger than 18 years of age or older than 50 years of age, any known sensitivity to either 2% lidocaine or 4% articaine or epinephrine, patients having active pain in more than 1 mandibular molar, subject taking any pain-relieving medication including over-the-counter analgesics at least 12 hours before enrollment in the study, and swelling near the tooth in question and having a tooth not suitable for simple restorative treatment because of extensive caries or periodontal problems.

Design outcomes

Primary

MeasureTime frame
endo ice efficacy as intra pulpal anesthetic agent in patient with symptomatic irreversible pulpitis after IANB with 2% lidocaine and buccal infiltration with 4% articaine.Timepoint: 1 hour

Secondary

MeasureTime frame
efficacy of primary block IANB with 2% lidocaine and buccal infiltration with 4% articaine as intrapulpal anaesthesiaTimepoint: 30 minutes

Countries

India

Contacts

Public ContactUMESH KUMAR

post graduate institute of medical education and research

odharmani911@gmail.com09862969792

Outcome results

None listed

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