NCT06483893 Ultrasound-Guided Thyroid Cartilage Plane Block vs Ultrasound-Guided Traditional Superior Laryngeal Nerve Block for Awake Fiberoptic Intubation in Patients With Limited Neck Mobility Undergoing Cervical Spine Fixation
| NCT ID | NCT06483893 |
| Status | Recruiting |
| Phase | — |
| Sponsor | Beni-Suef University |
| Condition | Patient Satisfaction |
| Study Type | INTERVENTIONAL |
| Enrollment | 50 participants |
| Start Date | 2024-07-01 |
| Primary Completion | 2024-07-01 |
Eligibility & Interventions
Eligibility Fast-Check
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What to Expect as a Participant
You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.
This trial targets 50 participants in total. It began in 2024-07-01 with a primary completion date of 2024-07-01.
⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.
Brief Summary
The aim of the work to compare between the effectiveness and safety of ultrasound-guided superior laryngeal nerve block through surface injection of local anesthetic solution on the thyroid cartilage and ultrasound-guided traditional superior laryngeal nerve block on quality of airway anesthesia for awake fiberoptic intubation in patients with limited neck mobility undergoing cervical spine fixation.
Eligibility Criteria
Inclusion Criteria: * patients aged between 18-65 years * either gender * ASA I-II * limited neck mobility Exclusion Criteria: * patients who refuse to give consent * non-cooperative patients * have asthma or ischemic heart disease * preoperative hoarseness, sore throat * mental or neurological disorders * contraindications for regional block (coagulopathy , infection at the needle insertion site and allergy to local anesthetics) * body mass index (BMI) \>26 kg/m2.
Contact & Investigator
Dina M Fakhry
PRINCIPAL INVESTIGATOR
Beni-Suef University
Frequently Asked Questions
Who can join the NCT06483893 clinical trial?
This trial is open to participants of all sexes, aged 18 Years or older, up to 65 Years, studying Patient Satisfaction. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.
Is NCT06483893 currently recruiting?
Yes, NCT06483893 is actively recruiting participants. Contact the research team at dina_fakhry_91@yahoo.com for enrollment information.
Where is the NCT06483893 trial being conducted?
This trial is being conducted at Banī Suwayf, Egypt.
Who is sponsoring the NCT06483893 clinical trial?
NCT06483893 is sponsored by Beni-Suef University. The principal investigator is Dina M Fakhry at Beni-Suef University. The trial plans to enroll 50 participants.