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Clinical Trials/CTRI/2024/11/076944
CTRI/2024/11/076944Not yet recruitingPhase 2

Randomized Controlled Trial to Evaluate the Anaesthetic Efficacy of Cryotherapy Application as an Adjunct to Articaine in Patients with Symptomatic Irreversible Pulpitis

SGT UNIVERSITY1 site in 1 country45 target enrollmentStarted: December 1, 2024Last updated:

Trial Snapshot

Phase
Phase 2
Status
Not yet recruiting
Enrollment
45
Locations
1
Primary Endpoint
To evaluate the anaesthetic efficacy of 4% articaine in IANB as compared to buccal infiltration techniques.

Study Overview

Brief Summary

AIM: Evaluation of anaesthetic efficacy of cryotherapy application as an adjunct to articaine in patients with symptomatic irreversible pulpitis.OBJECTIVE: To evaluate the anaesthetic efficacy of 4% articaine in IANB as compared to buccal infiltration techniques. To compare the anaesthetic efficacy of cryotherapy as an adjunct to articaine and determine the best technique that provide maximum success in patients with symptomatic irreversible pulpitis.MATERIALS AND METHOD The proposed study will be conducted at Department of Conservative Dentistry and Endodontics, Faculty of Dental Sciences, SGT University, Gurugram, Haryana after the approval from the ethical committee.PATIENT SELECTION: GROUP 1 (n 15) Inferior alveolar nerve block with articaine. GROUP 2 (n 15) Inferior alveolar nerve block with articaine plus application of ice stick in the pulp chamber. GROUP 3 (n 15) Buccal infiltration with articaine plus application of ice stick in the pulp chamber.There is paucity of clinical studies in evaluating the anaesthetic efficacy of cryotherapy application as an adjunct to articaine in patients with symptomatic irreversible pulpitis. Thus, the purpose of current randomized controlled trial is evaluation of anaesthetic efficacy of cryotherapy application as an adjunct to articaine in patients with symptomatic irreversible pulpitis. RESULTS: On going research CONCLUSION: On going research

Study Design

Study Type
Interventional
Allocation
Coin toss, Lottery, toss of dice, shuffling cards etc
Masking
Participant and Outcome Assessor Blinded

Eligibility Criteria

Ages
18.00 Year(s) to 57.00 Year(s) (—)
Sex
All

Inclusion Criteria

  • Mature permanent mandibular molars diagnosed with symptomatic irreversible pulpitis.
  • Teeth having sufficient tooth structure for adequate isolation.
  • No history of previous endodontic therapy.

Exclusion Criteria

  • Immunocompromised patients, pregnant and lactating females.
  • Periodontally compromised teeth.
  • Patients with pulp necrosis, periapical radiolucency, sinus tract, and periapical abscess.
  • Allergy, sensitivity or contraindications to articaine.
  • Patients who had taken analgesics within 12 hours before root canal therapy.

Outcomes

Primary Outcomes

To evaluate the anaesthetic efficacy of 4% articaine in IANB as compared to buccal infiltration techniques.

Time Frame: Baseline, 30mins and 1hour

Secondary Outcomes

  • To compare the anaesthetic efficacy of cryotherapy as an adjunct to articaine & determine the best technique that provide maximum success in patients with symptomatic irreversible pulpitis.(Baseline, 30mins & 1hour)

Investigators

Sponsor Class
Research institution and hospital
Responsible Party
Principal Investigator
Principal Investigator

KHUSHBU

SGT DENTAL COLLEGE HOSPITAL AND RESEARCH INSTITUTE

Study Sites (1)

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