ClinicalTrials.gg
Status unknownNCT06167187Updated Dec 12, 2023

The Effect of Inferior Alveolar Nerve Block in Fracture Mandibular Surgeries

An interventional study of bilateral inferior alveolar nerve block and Ketorolac and fentanyl in Anesthesia, sponsored by Ain Shams University. Status unknown at 1 site in Egypt. Open to participants aged 18 Years to 65 Years. Per ClinicalTrials.gov, last updated 2023-12-12.

Sponsored by Ain Shams University · Not applicable, Interventional, and Treatment

The sponsor has not verified this record recently (last verified Dec 2023), so the status shown — last known as Recruiting — may be out of date.

From the registry’s dates

  • Registered 6 months after the study started (first participant enrolled Jun 2023, registered Dec 2023).
Phase
Not applicable
Study type
Interventional
Enrollment
46
Allocation
Randomized
Ages
18 Years to 65 Years
Sex
All
01

Study summary

The aim of the study is to assess the efficacy of adding of pre-emptive inferior alveolar nerve block compared to the conventional systemic intravenous analgesia in controlling perioperative pain in fracture mandibular surgeries.

Read the detailed description

Opioid drug administration is a common technique to reduce pain from surgical trauma. However, the use of large doses of opioid drugs during and after surgery can be associated with an increased incidence of multiple side effects such as; ventilatory depression, sedation, nausea, vomiting, pruritus, difficult voiding and ileus.

In maxillofacial surgeries in which patients often receive maxillomandibular fixation these side effects are troublesome to the patient and at worst case scenario can cause a life-threatening complications. Ventilatory depression and vomiting are the most serious side effects especially in early postoperative hours. Various methods have been proposed to minimize these side effects. Nerve block with long-acting local anesthesia is a proposed technique in this regard.

In maxillofacial operations, bupivacaine is a highly efficient long-acting local anesthetic and has been used as a safe local anesthetic for neuroanalgesia after cleft lip operation or third molar surgery alone or in combination with low-power laser and diclofenac.

Inferior alveolar nerve block is considered as gold standard for sensory block of the hemi mandible. It can provide adequate anesthesia and analgesia for one side of the mandibular teeth and gingival mucosa, the body and inferior ramus of the mandible, the anterior two-thirds of the tongue and floor of the mouth cavity.

The inferior alveolar nerve (IAN) block is a widely used regional anaesthetic nerve block for the mandible. The most commonly used technique for IAN block is called the direct approach which include inserting the needle into the pterygomandibular raphae by penetrating the buccinators muscle. Once in this space, the aim is to inject the local anaesthetic solution besides the inferior alveolar nerve before it enters the mandibular foramen.

02

Conditions studied

  • Anesthesia
03

In context

Lead sponsor

Ain Shams University is the lead sponsor of 1,930 studies on the registry; 433 are open to participants now.

Of its 33 completed or terminated interventional studies of FDA-regulated products, 0 (0%) have results posted.

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

04

Who can participate

Ages eligible
18 Years to 65 Years
Sexes eligible
All
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  1. Age group: 18 - 65 years old.
  2. American Society of Anesthesiologists (ASA) Physical Status Class I to III
  3. Scheduled for fracture mandible fixation.

Exclusion criteria

Exclusion Criteria:

  1. Refusing to participate in the study.
  2. History of allergy to the medications used in the study.
  3. Contraindications to regional anesthesia (including coagulopathy and local infection).
  4. Psychiatric disorders.
  5. Pregnancy.
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Double (Participant, Care provider)
Enrollment
46 participants (estimated)

Study arms

  • Active comparator
    Study group (IAN block group)

    patients will receive bilateral inferior alveolar nerve block. 23 patients

    Procedure: bilateral inferior alveolar nerve block

  • Active comparator
    control group

    patients will not receive the block and will receive intravenous multimodal analgesia according to standard protocol. 23 patients

    Drug: Ketorolac and fentanyl

Interventions

  • Procedurebilateral inferior alveolar nerve block

    Placing the tip of the thumb or forefinger into the coronoid notch (retromolar fossa) to help visualize the vertical height at which the needle will enter, and retracting the cheek to expose the pterygomandibular triangle. Placing the barrel of the syringe over the contralateral lower 1st and 2nd premolars and resting the side of the needle tip against the lateral edge of the pterygomandibular raphe, aiming the tip of the needle into the pterygomandibular triangle, with the bevel facing the ramus. Advancing the needle tip slightly into the mucosa until it is stopped by the ramus (typically after about 2 to 2.5 cm of insertion) and withdrawing needle 1 mm away from bone. Aspirating to rule out intravascular placement. If aspiration reveals intravascular placement, withdrawal of the needle will be done 2 to 3 mm, then reaspirating prior to injection. Slowly injecting about 2 to 4 milliliters of bupivacaine 0.5% anesthetic in each side..

    Also known as: IANB

  • DrugKetorolac and fentanyl

    Drug pages: Ketorolac · Fentanyl

    in control group, Patients will not receive the block and pain will be controlled according to institutional protocol using 30 mg ketorolac IV and fentanyl increments as needed.

06

What researchers measure

Primary outcomes

  1. The time of the first dose of fentanyl rescue analgesia intraoperative

    guided by hemodynamic changes

    Time frame: Throughout the surgery

  2. Total amount of additional intraoperative fentanyl rescue analgesia

    guided by hemodynamic changes

    Time frame: Throughout the surgery

  3. The time from recovery to the first dose pethidine rescue analgesic

    guided by visual analogue scale.

    Time frame: 24 hours postoperatively

  4. Total amount of pethidine postoperative rescue analgesic

    guided by visual analogue scale.

    Time frame: 24 hours postoperatively

Secondary outcomes

  1. Incidence of complications related to the block

    Time frame: 24 hours postoperatively

07

Study locations

1 of 1 sites recruiting
  • Faculty of medicine - Ain shams university hospitals
    Cairo, 11591, Egypt
    Recruiting
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reached

Started Jun 2023 (actual). Primary completion is estimated for Apr 2024, 10 months after the start.

How these figures are worked out, and which studies are left out of them.

Registered
Dec 2, 2023
First posted
Dec 12, 2023
StartActual
Jun 1, 2023
Primary completionEst.
Apr 2024
CompletionEst.
Jun 2024
Last update
Dec 12, 2023
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Dec 12, 2023, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT06167187
Responsible party
mohamed atef (assistant lecturer of anesthesia, Ain Shams University) — Principal investigator
First posted
Dec 12, 2023
Start date
Jun 1, 2023
Primary completion
Apr 2024 (estimated)
Completion
Jun 2024 (estimated)
Last update
Dec 12, 2023

Study contacts

Mohamed Atef, ass.lecturer
Contact
Moahmed.Atef@med.asu.edu.eg
00201065270020
Mohamed Atef, ass.lecturer
principal investigator · faculty of medicine, ain shams university

Oversight

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

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