Comparison of Osteocentral Versus Locoregional Anesthesia in Case of Mandibular Molar Pulpitis

NCT ID: NCT03802305

Last Updated: 2022-06-28

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

72 participants

Study Classification

INTERVENTIONAL

Study Start Date

2019-03-01

Study Completion Date

2022-06-17

Brief Summary

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The irreversible acute pulpitis is the most common emergency at the hospital during dental consultation. Pulpitis are characterized by intense and spontaneous oro-facial pains. In case of mandibular molar, the emergency treatment consists in realizing a pulpotomy (eviction of cameral pulp) under locoregional anesthesia called inferior alveolar nerve block (IANB). The latter represents a real challenge, since inflammation may decrease its action. To mitigate this deficiency and the drawbacks of the IANB (onset and duration of the anesthesia, bites risk reported with IANB) other anesthesias are proposed. In particular the computerized intraosseous technique anesthesia of which the Quicksleeper™ system is a part. However, according to the observers, a mild to severe tachycardia have been reported.

Very few valid clinical trials exists on the subject, most being realized with systems of intraosseous anesthesia other than Quicksleeper™. Therefore, the aim of this study is first to analyze the variations of the cardiovascular parameters into two groups of anesthesia: locoregional anesthesia and Quicksleeper ™ system; and then, to compare the efficiency, side effects, operating consequences of both techniques. This study should provide better data about potential risk with computerized intraosseous technique such has Quicksleeper ™ system in healthy or cardiovascular risk patient.

Detailed Description

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When the patient arrive in the dental care center, an initial assessment is made to get the diagnosis of irreversible pulpitis:

1. Anamnesis:

acute and spontaneous oro-facial pain, pulsatile severe intensity, which could irradiate toward the ear and/or jaw, exacerbated by cold or hot.
2. Clinical exams: positive vitality tests (electric test and cold pressor test)
3. Further examination (radiography)

The inclusion and exclusion criteria will be checked and the informed consent of the patient will be taken. The patient is then randomized in one of the group (experimental or control). He will fill a questionnaire (Corah's scale) for evaluating his state of anxiety during care. A monitoring of cardiac parameters is made during the care at defined moment.

The patient evaluates his pain himself with the VAS (Visual Analog Score), before the intervention. The anesthesia is carried out by only one experimenter, with the Quickslepper™ handpiece but different specific needles.

Each patient receive 1.8 mL of 4% articaine 1:100 000 on a period of 2 minutes.

Conditions

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Endodontic Inflammation

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Number of Arms: 2 Masking: Simple Blinded, Masked Roles: Subject Allocation: Randomized Study Endpoint Classification: Interventional Research with Minimal Risk and Constraints, Safety/Efficacy Enrollment: subjects (anticipated)
Primary Study Purpose

TREATMENT

Blinding Strategy

SINGLE

Participants

Study Groups

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Computerized intraosseous technique (Quicksleeper™)

patients will receive the anesthetic solution with computerized intraosseous technique anesthesia near the tooth roots involved.

Group Type EXPERIMENTAL

computerized intraosseous technique (Quicksleeper™)

Intervention Type DEVICE

The anesthetic solution is administered with a specific equipment allowing the injection step by step:

* anesthesia of the interdental papilla,
* positioning of the needle and perforating of the interdental space,
* Injection of the solution. All of these steps are based on an adjustment of the different part of this equipment.

loco-regional anesthesia (IANB technique)

patients will receive the anesthetic solution with the loco-regional anesthesia technique: near the place where the nerve goes into the jaw, based on osteo muscular markers.

Group Type ACTIVE_COMPARATOR

loco-regional anesthesia (IANB technique)

Intervention Type DEVICE

The anesthetic solution is delivered by a needle near to the inferior alveolar nerve before it enters the mandibular foramen.

Interventions

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computerized intraosseous technique (Quicksleeper™)

The anesthetic solution is administered with a specific equipment allowing the injection step by step:

* anesthesia of the interdental papilla,
* positioning of the needle and perforating of the interdental space,
* Injection of the solution. All of these steps are based on an adjustment of the different part of this equipment.

Intervention Type DEVICE

loco-regional anesthesia (IANB technique)

The anesthetic solution is delivered by a needle near to the inferior alveolar nerve before it enters the mandibular foramen.

Intervention Type DEVICE

Eligibility Criteria

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Inclusion Criteria

* real irreversible pulpitis of a mandibular molar in dental emergency consultation at the Nantes hospital
* Healthy patient without medical history (ASA 1), without treatment for heart rate distress (anti arrhythmic, beta-blocking drug)
* Major and covered by the social security
* Informed consent

Exclusion Criteria

* ASA \> 1
* Pregnant and breastfeeding women
* Minors
* Adults under guardianships
* Adults deprived of freedom
* Impossibility to obtain for informed consent
* Allergy to anesthetic components
* Contraindication of vasoconstrictor
* Angle closure glaucoma

* Pheochromocytomas
* Bisphosphonate IV
* Irradiated patient (upper respiratory and gastrointestinal tract cancer)
* Contraindication with Mono-amino oxidase inhibitors
* Acute apical periodontitis
* Pulpitis on wisdom teeth
* Vital teeth with fixed prosthesis
* Active periodontal disease
* Local anatomic difficulty
* No reference tooth for vitality dental test
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Nantes University Hospital

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Locations

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Nantes Universitary Hospital

Nantes, Loire-Atlantique, France

Site Status

Countries

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France

References

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Gaudin A, Clouet R, Boeffard C, Laham A, Martin H, Amador Del Valle G, Enkel B, Prud'homme T. Comparing intraosseous computerized anaesthesia with inferior alveolar nerve block in the treatment of symptomatic irreversible pulpitis: A randomized controlled trial. Int Endod J. 2023 Aug;56(8):922-931. doi: 10.1111/iej.13935. Epub 2023 May 29.

Reference Type DERIVED
PMID: 37209243 (View on PubMed)

Laham A, Clouet R, Del Valle GA, Gaudin A, Prud'homme T. Anaesthetic efficacy and influence on cardiovascular parameters change of intraosseous computerised anaesthesia versus inferior alveolar nerve block anaesthesia in acute irreversible pulpitis of mandibular molars: study protocol for a prospective randomised controlled trial. Trials. 2022 Dec 5;23(1):979. doi: 10.1186/s13063-022-06915-4.

Reference Type DERIVED
PMID: 36471427 (View on PubMed)

Other Identifiers

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RC18_0268

Identifier Type: -

Identifier Source: org_study_id

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