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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT06443255
Other study ID # 2023-506644-17
Secondary ID
Status Not yet recruiting
Phase Phase 3
First received
Last updated
Start date June 2024
Est. completion date September 2024

Study information

Verified date June 2024
Source Rigshospitalet, Denmark
Contact Mo H Larsen, MD
Phone +4535456589
Email mo.haslund.larsen.02@regionh.dk
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

When performed by trained personnel nasotracheal intubation is a safe and effective technique for attaining a secure airway in preparation for surgery of the head and neck. The procedure can be deemed necessary due to the nature of the surgical procedure or considerations in regard to the patient's comorbidities. For a certain group of patients with expected difficult airways, the procedure is done whilst they are awake and aided by fiberoptics. For these awake patients, extra precautions must be taken to ensure the procedure is conducted with minimal pain and discomfort. The pain and discomfort arises from the mechanical manipulation of the nasal mucosa and can be alleviated in part by means of topical analgesia as well as through decongestion, providing more space within the nasal cavity. For these purposes, several drugs in varying combinations and dosages are used, but no single drug choice is universally recommended. Cocaine is one of these appropriate drugs. It is a magistral formula used especially due to its unique combination of both vasoconstrictive and analgesic properties. Concerns have though been raised regarding cocaine's potential toxicity and alternative medications are continuously sought after. A combination of lidocaine and xylometazoline can also be used for preparation of the nose prior to awake nasal fiberoptic intubation. Lidocaine contributes with its analgesic effect whilst xylometazoline functions as the vasoconstrictor. The investigators wish to compare the analgesic effects of cocaine and lidocaine/phenylephrine to each other and saline when subjectively scored on a visual analogue scale of 0-100 mm immediately after simulated awake nasal intubation on healthy volunteers.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 12
Est. completion date September 2024
Est. primary completion date September 2024
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Age = 18 years - Proficient in spoken and written Danish - Healthy volunteers (no active diagnoses) - Negative hCG (human chorionic gonadotropin) urine stix for women of childbearing potential Exclusion Criteria: - Known nasal malformation - Known coagulopathy - Current antithrombotic treatment - Self-reported epistaxis occurring more than once a month - Symptoms of a common cold within the past week - Hypersensitivity to local anaesthetics of amide type or any of the excipients - Hypertension - Narrow-angle glaucoma

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Cociane hydrochloride 4%
2 mL of 4% cocaine
Lidocaine 4%
1.5 mL of 4% lidocaine
Xylometazoline 0.1%
0.5 mL of xylometazoline 0.1%
Saline 0.9%
2 mL of saline 0.9%

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Rigshospitalet, Denmark

Outcome

Type Measure Description Time frame Safety issue
Primary Pain regarding the procedure Self reported pain on a visual analogue scale of 0-100 mm Immediately following the procedure of 10 cm insertion of a 6.0 nasal endotracheal tube
Secondary Pain regarding the procedure Self reported pain on a visual analogue scale of 0-100 mm One minute after the procedure of insertion of a 6.0 nasal endotracheal tube
Secondary Volume Volume within both nasal cavities measured with acoustic rhinometry 5 minutes before drug administration and 1, 3, 5, 7 and 9 minutes after drug administration
Secondary Fiberoptic endoscopy Preferred nasal cavity based on a comparison of the degree of vasoconstriction of the nasal mucosa evaluated by fiberoptic endoscopy assessed by ENT-specialist Fiberoptic endoscopy performed 10 minutes before drug administraion and 10 minutes after drug administration
Secondary Drug test detection Concentraion of cocaine and cocaine's main metabolite benzoylecgonine in blood and saliva samples respectively 15 minutes before drug administration and 1, 2 and 3 hours after drug administration
Secondary Heart rate Measurement of heart rate 5 minutes before drug administration and 1, 2, 3, 4 and 5 minutes after drug administration
Secondary Blood pressure Measurement of mean arterial blood pressure 5 minutes before drug administration and 1, 2, 3, 4 and 5 minutes after drug administration
Secondary Patient-centred questions The degree of discomfort and unpleasentness of taste of the drug administration on a scale of 1-10 and whether they felt exaltation after drug administration. 15 minutes after drug administration
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