Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
Healthy Volunteers
ID07130760

Is Intraligamentary Injection the Anesthesia of Choice for Symptomatic Irreversible Pulpitis in Mandibular Molars? A Multicenter Randomized Comparative Trial.

Led by Aula Dental Avanzada · Updated on 2025-08-19

52

Participants Needed

2

Research Sites

4 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The trial investigates two methods of anesthesia for patients with symptomatic irreversible pulpitis in mandibular molars, a condition that makes pain control during dental treatment challenging. This randomized study aims to compare the effectiveness of intraligamentary injection and inferior alveolar nerve block in controlling pain during endodontic access. The research is conducted across multiple dental centers using standardized criteria and validated pain scales. Participants will be randomly assigned to receive either intraligamentary anesthesia with 2% lidocaine and epinephrine using a dental syringe or the conventional inferior alveolar nerve block with the same anesthetic solution. These procedures are administered before the dental access to evaluate which technique better eliminates pain. The study is single-blinded and includes follow-up measures at the end of treatment and seven days later. During the trial, pain will be assessed immediately after access cavity preparation. Additional measurements include the need for supplementary anesthesia during the procedure, patient satisfaction both immediately and at seven days post-treatment, and postoperative pain at seven days. Participants will be monitored through follow-up visits and data collection to evaluate the outcomes and safety of each anesthesia method. The total participation time includes the initial treatment and a one-week follow-up.

CONDITIONS

Brief Title

Intraligamentary vs Inferior Alveolar Nerve Block for Pulpitis: A Randomized Clinical Trial

Who Can Participate

Age: 18Years +
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Adults aged 18 years or older
  • Presenting with symptomatic irreversible pulpitis in a mandibular molar
  • Vital response to cold testing
  • Ability to understand and provide informed consent
  • Available for follow-up and data collection
Not Eligible

You will not qualify if you...

  • Known allergy to lidocaine or epinephrine
  • Pregnancy or breastfeeding
  • Use of analgesics or anti-inflammatory drugs in the previous 6 hours
  • Non-vital or previously treated teeth
  • Significant systemic disease (ASA III or above)
  • History of psychiatric or neurological disorders affecting pain perception

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

Treatment

Duration - Single treatment visit

Participants receive either intraligamentary injection or inferior alveolar nerve block anesthesia prior to endodontic access to treat symptomatic irreversible pulpitis in mandibular molars.

1 visit (in-person)

Follow-up

Duration - 7 days after treatment

Participants are monitored for postoperative pain and satisfaction after treatment.

1 follow-up visit

Trial Site Locations

Total: 2 locations

1

Clínica Dental 4

Ferrol, A coruña, Spain, 15402

Actively Recruiting

2

Clínica Dental Esteve

Alicante, Alicante, Spain, 03001

Actively Recruiting

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Research Team

G

Guillem Esteve-Pardo, PhD

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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