Xylometazoline and Cocaine for Nasal Vasoconstriction

Sponsor
Rigshospitalet, Denmark (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT05334017
Collaborator
(none)
110
1
2
12
9.2

Study Details

Study Description

Brief Summary

The objective of this study is to compare xylometazoline and cocaine's effect on minimizing epistaxis when administered as a local vasoconstrictor prior to nasal intubation.

The investigators hypothesize that there will be a lower bleeding score in the group receiving xylometazoline as compared with the group receiving cocaine.

Condition or Disease Intervention/Treatment Phase
  • Drug: Xylometazoline 0,1%
  • Drug: Cocaine 4%
Phase 4

Detailed Description

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. Upon intubation the nasal mucosa must be sufficiently lubricated and decongested in order to minimize the risk of epistaxis. For this purpose several topical agents are suggested, the most common being adrenaline, cocaine and oxymetazoline/xylometazoline in varying combinations and dosages. As such, no broad consensus or guidelines currently exist on a single recommended drug for the prevention of epistaxis induced by nasal intubation.

In 1990 Katz et. al performed a study comparing three interventions: cocaine, lidocaine with epinephrine and oxymetazoline in regard to the prevention of epistaxis on nasotracheal intubation. This study included 14 patients in each of their three groups and the authors concluded that oxymetazoline and cocaine were equally effective. However, due to their limited sample size that study was clearly inconclusive, and the investigators wish to repeat such a comparison.

The trial drug xylometazoline is commonly used in Danish operating rooms under the registered trademark Zymelin. It is an adrenergic drug typically used for decongestion of the nose and its local vasoconstrictive effect occurs after a few minutes and lasts 10-12 hours. The drug is readily available without prescription and in theory the patient could administer this themselves on their way to surgery. Oxymetazoline used by Katz et. al and xylometazoline used in Danish hospitals have similar decongestive effects as oxymetazoline is a derivative of xylometazoline. The two drugs share pharmacodynamics varying only on receptor subtype affinity in their direct action on alpha-adrenergic receptors in the arterioles of the nasal mucosa. Both drugs result in vasoconstriction that leads to decreased blood flow and thereby decongests the nose.

The second trial drug cocaine is also routinely used. It is a magistral formula used especially due to its unique combination of both vasoconstrictive and analgesic properties. It is a potent vasoconstrictor through its ability to inhibit the reuptake and metabolism of catecholamines, which then in greater concentration produce adrenergic effects. Uniquely cocaine also binds to and blocks axonal membrane sodium channels, thus interfering with the propagation of action potentials and thereby exerting an analgesic effect. When administered in doses thought to avoid systemic effects, cocaine is a safe local anesthetic agent. The recommended dosage varies considerably throughout the literature with safe doses ranging between 1.5-3.0 mg/kg.

The investigators wish to compare the effects of xylometazoline and cocaine regarding their prevention of epistaxis during and immediately after nasal intubation.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
110 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Triple (Participant, Care Provider, Outcomes Assessor)
Primary Purpose:
Prevention
Official Title:
Comparison of the Effect of Xylometazoline and Cocaine on Epistaxis When Administered as Local Vasoconstrictors Prior to Nasal Intubation
Anticipated Study Start Date :
Jun 1, 2022
Anticipated Primary Completion Date :
Jun 1, 2023
Anticipated Study Completion Date :
Jun 1, 2023

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: Xylometazoline

Xylometazoline 0,1% as nasal solution given immediately prior to nasal intubation

Drug: Xylometazoline 0,1%
1 ml of 0,1% xylometazoline diluted with 1 ml of 0,9% isotonic saline solution given as a nasal spray
Other Names:
  • Zymelin
  • Active Comparator: Cocaine

    Cocaine 4% as nasal solution given immediately prior to nasal intubation

    Drug: Cocaine 4%
    2 ml of 4% cocaine given as a nasal spray
    Other Names:
  • Cocaine hydrochloride 4%
  • Outcome Measures

    Primary Outcome Measures

    1. Bleeding score [Immediately following nasal intubation]

      Evaluation of epistaxis measured on a predefined scale of 0-3: 0. No sign of bleeding Blood only on the tracheal tube Pooling of blood in the pharynx Bleeding to the extent that it complicates intubation

    Secondary Outcome Measures

    1. Qualitative measurements of cocaine's main metabolite benzoylecgonine in saliva [Immediately prior to nasal intubation, 60 minutes after administration of cocaine and 24 hours after administration of cocaine.]

      For cocaine-group only, saliva samples will be obtained and analyzed on the DrugTest 5000 machine used by the Danish Police Force in order to evaluate pharmacokinetics.

    2. Quantitative measurements of cocaine in whole blood. [Immediately prior to nasal intubation, 60 minutes after administration of cocaine and 24 hours after administration of cocaine.]

      In the cocaine group only, blood samples will be drawn and analyzed for the presence of cocaine in order to evaluate pharmacokinetics.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • Age ≥ 18 years

    • Scheduled for nasal intubation

    • Proficient in spoken and written Danish

    Exclusion Criteria:
    • Intubation to be done on awake patient

    • Pregnancy

    • Women of childbearing potential must produce a negative hCG urine stix to participate

    • Known symptomatic coronary artery disease

    • As declared by patient or noted in the patient's file

    • Untreated hypertension

    • As declared by patient or noted in the patient's file

    • Not taking antihypertension drugs

    • Hypersensitivity to the active substance or to any of the excipients of Zymelin

    • As declared by patient or noted in the patient's file

    • Closed-angle glaucoma

    • As declared by patient or noted in the patient's file

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Rigshospitalet, Copenhagen University Hospital Copenhagen Denmark 2100

    Sponsors and Collaborators

    • Rigshospitalet, Denmark

    Investigators

    • Principal Investigator: Mo Haslund Larsen, MD, Rigshospitalet, Denmark

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Mo Haslund Larsen, Principal investigator, Rigshospitalet, Denmark
    ClinicalTrials.gov Identifier:
    NCT05334017
    Other Study ID Numbers:
    • 89303200
    • 2021-000691-11
    • H-21028051
    First Posted:
    Apr 19, 2022
    Last Update Posted:
    Apr 27, 2022
    Last Verified:
    Apr 1, 2022
    Individual Participant Data (IPD) Sharing Statement:
    No
    Plan to Share IPD:
    No
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Keywords provided by Mo Haslund Larsen, Principal investigator, Rigshospitalet, Denmark
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Apr 27, 2022