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WithdrawnNCT04961554OBlocUpdated Feb 3, 2023

Evolution of Mouth Opening After Mandibular Block

An observational study in Trismus, sponsored by Assistance Publique - Hôpitaux de Paris. Withdrawn at 1 site in France. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2023-02-03.

Sponsored by Assistance Publique - Hôpitaux de Paris · Observational

Why this study was withdrawn
1. Short defense deadline 2. Activity cessation of the maxillofacial surgery department at Pitié Salpêtrière hospital
Study type
Observational
Model
Other
Time perspective
Prospective
Enrollment
0
Ages
18 Years and older
Sex
All
01

Study summary

Trismus is an involuntary contracture of the masticatory muscles, blocking the opening of the jaw, first intermittent then permanent and irreducible. Trismus is the result of pain or spasm or even muscle fibrosis, due to infectious, inflammatory or tumoral involvement of the masticatory muscles.

During any anesthesia, control of the patient's upper airways is a major issue. Orotracheal intubation is the gold standard. Trismus will therefore complicate this management of the airways. This trismus can prevent the realization of a classic intubation, by the inability to use a laryngoscope or video laryngoscope, in favor of awake fiberoptic intubation, a technique that causes discomfort during the procedure, then a state of post-traumatic stress.

Mandibular block is increasingly used in the analgesia of mandibular surgeries thanks to the simplicity of the technique and its good efficiency. It has been described that the mandibular locoregional anesthesia made it possible to remove the trismus due to a dental infection, allowing the realization of a surgical gesture under good conditions. In addition, authors have described V3 block as a technique that could improve the safety of anesthesia in patients with acute trismus, by avoiding the need for awake nasofibroscopy intubation. One study showed that performing locoregional anesthesia of the mandibular nerve improved the mouth opening in patients with mandibular fracture. The investigators wondered if this locoregional anesthesia could also work on other types of trismus such as infectious, tumoral and osteoradionecrosis trismus.

During preoperative consultation, anesthesists usually measure the mouth opening. In our study, anesthesists will also measure the mouth opening after performing locoregional anesthesia of the V3 nerve (mandibular block). In addition to the measurement made before the start of the anesthetic treatment, research provides for three other measurements of the mouth opening using a rule (millimeters), taken at different times : after sedation, after performing locoregional anesthesia and after curarization. The investigators will also collect the cause of the limited mouth opening, the duration of development. The investigators will study pain at rest and when opening the mouth, under sedation, when performing the block, then when opening the mouth after performing the block. The presence of edema next to the area of locoregional anesthesia, the type of product used for sedation and locoregional anesthesia, the intubation technique performed, as well as the difficulty experienced by the operator will be collected

Read the detailed description

The aim of this study is to avoid recourse to awake fiberoptic intubation, which causes discomfort during the procedure and post-traumatic stress disorder, in patients with a very limited mouth opening (less than 20mm) and who must undergo anesthesia general for mandibular surgery.

As a reminder, the definition of limited mouth opening (MO) is a lower 35mm mouth opening, according to the Société française d'anesthésie-réanimation (SFAR) recommendations. The investigators define a very limited mouth opening as a mouth opening that does not allow a video laryngoscope blade to be inserted into the patient's mouth (less than 20mm).

During preoperative consultation, anesthesists usually measure the mouth opening. In our study, anesthesists will also measure the mouth opening after performing locoregional anesthesia of the V3 nerve (mandibular block). In addition to the measurement made before the start of the anesthetic treatment, research provides for three other measurements of the mouth opening using a rule, taken at different times.

The management is carried out exclusively by the investigators, the latter being anesthetists. Thus, the evaluation of the different mouth openings using a ruler (in millimeters), the evaluation of the pain using the numerical scale, the administration of sedation, the realization of loco-regional anesthesia, intraoperative and postoperative anesthetic management will be carried out by one and the same person qualified in anesthesia for maxillofacial surgery.

In summary, six key steps for our study will be carried out by the anesthetist-resuscitator:

  1. Initial patient assessment with assessment of pain and mouth opening (millimeters)
  2. Introduction of sedation, and reassessment of pain and mouth opening (millimeters)
  3. Performing a locoregional anesthesia of the V3 for analgesic purposes
  4. Reassessment of pain, mouth opening (millimeters) at least 15 minutes from the block, and possibly the Mallampati score. Mallampati score is systematically noted as part of the treatment.
  5. Induction of anesthesia, and reassessment of the mouth opening after curarization.
  6. Assessment of the difficulty of intubation (difficulty in passing the videolaryngoscope blade, Cormack score applied to videolaryngoscopy).

The anesthetist who performs the locoregional anesthesia will collect the data using the standardized questionnaire created for the study, notifying the key clinical elements of airway management that are being research within the framework of care, according to the rules of good anesthesia practice.

These data, collected as part of the treatment, will be:

  • The cause of the limited mouth opening
  • The duration of development
  • Pain at rest and when opening the mouth, then under sedation, when performing the block, then when opening the mouth after performing the block, using the digital scale
  • The presence of edema next to the area of locoregional anesthesia of V3
  • The type of product used for sedation and locoregional anesthesia
  • The mouth opening (measured in millimeters using a ruler) before any gesture then after sedation, 15 minutes from the completion of the V3 nerve block, and after curarization.
  • The investigators will also evaluate the evolution of the Mallampati score at the same time, as part of the treatment.
  • The intubation technique performed, as well as the difficulty experienced by the operator.

These data will be pseudonymized.

02

Conditions studied

  • Trismus

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Keywords

  • mandibular block
  • limited mouth opening
  • trismus
  • loco-regional anesthesia
  • pain
  • video laryngoscope
  • awake flexible fiberoptic intubation
  • difficult airway management
  • head and neck surgery
  • maxillofacial surgery
03

In context

Trismus

88 studies on the registry are indexed under Trismus; 16 are open to participants now.

Browse Trismus studies →

Lead sponsor

Assistance Publique - Hôpitaux de Paris is the lead sponsor of 3,506 studies on the registry; 1,007 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

Adult patients presenting with a limited mouth opening that does not allow intubation by videolaryngoscopy, with mandibular surgical pathology requiring general anesthesia

Inclusion criteria

  • Age ≥ 18 years old
  • Patient with a mouth opening defined as very limited (\<20mm)
  • Patient scheduled for mandibular surgery, with an indication for a V3 block for analgesic purposes
  • Patient informed and not opposed to the study

Exclusion criteria

Exclusion Criteria:

  • Allergy to local anesthetics
  • Patient under judicial protection
05

Study design

Observational model
Other
Time perspective
Prospective
Enrollment
0 participants (actual)
Patient registry
No

Groups and cohorts

  • Adult patients presenting with limited mouth opening

    Adult patients presenting with limited mouth opening not allowing intubation by videolaryngoscopy, on mandibular surgical pathology requiring general anesthesia.

    Other: loco-regional anesthesia

Interventions

  • Otherloco-regional anesthesia

    demonstrate that the mouth opening (measured in millimeters) of a patient treated for mandibular surgery with a very limited opening (defined by a threshold less than 20mm, not allowing the passage of a video laryngoscope blade per route buccal) is more important after locoregional anesthesia of the V3 than before anesthesia.

06

What researchers measure

Primary outcomes

  1. Measure of patient's mouth opening

    The main outcome is the measure of patient's mouth opening (in millimeters) in the minutes preceding and following the mandibular block. The mouth opening will be measured using a ruler with 4 defined times: * Before any anesthesia * After sedation * 15min from the realization of the loco-regional anesthesia * After curarization, just before intubation. These different measurements will be carried out by a ruler, and by a single operator for these 4 measurements.

    Time frame: during surgery

Secondary outcomes

  1. Assessement of Etiology of limited mouth opening (osteoradionecrosis, tumor, infection)

    Potentially predictive of the success of locoregional anesthesia on mouth opening

    Time frame: during surgery

  2. Mallampati score

    Predictive of intubation difficulty

    Time frame: before locoregional anesthesia

07

Study locations

1 site
  • Anesthésie-Réanimation Pôle Tête et Cou, Hôpital Pitié-Salpêtrière
    Paris, France
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Feb 3, 2023, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT04961554
Lead sponsor
Assistance Publique - Hôpitaux de Paris
Responsible party
Sponsor
First posted
Jul 14, 2021
Start date
Apr 2, 2023 (estimated)
Primary completion
Apr 2, 2024 (estimated)
Completion
Apr 2, 2024 (estimated)
Last update
Feb 3, 2023

Study contacts

Claire Gourbeix, MD
principal investigator · Assistance Publique - Hôpitaux de Paris

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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