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Nebulized Scopolamine for Motion Sickness
Phase 1
Recruiting
Led By Jay C Buckey, Ph.D
Research Sponsored by Dartmouth-Hitchcock Medical Center
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Normal weight for body size, based on BMI table
Renal and hepatic function within normal ranges
Must not have
Drug allergies to scopolamine or other belladonna alkaloid
Significant deviated septum that blocks air flow in one nostril
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 180 minutes
Awards & highlights
All Individual Drugs Already Approved
Summary
This trial is testing a new way to give anti-motion sickness medicine by spraying it into the nose. It targets people who get motion sickness and aims to provide faster relief by allowing quick absorption through the nasal tissues.
Who is the study for?
Adults aged 21-49 in good health, with normal weight and organ function, can join this trial. They must not have used investigational drugs recently, smoked tobacco within a year, or lost significant blood lately. Pregnant women and those on certain medications or with specific medical conditions like respiratory issues or drug allergies are excluded.
What is being tested?
The study is testing the effectiveness of delivering Scopolamine through an intranasal nebulizer to prevent motion sickness compared to a placebo (a treatment with no active drug). Participants will receive either the real medication or placebo without knowing which one they're getting.
What are the potential side effects?
Scopolamine may cause dry mouth, dizziness, blurred vision, and drowsiness. Less common side effects include confusion and difficulty urinating. The placebo is unlikely to cause any side effects since it doesn't contain an active drug.
Eligibility Criteria
Inclusion Criteria
You may be eligible if you check “Yes” for the criteria belowSelect...
My weight is normal for my height.
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My kidney and liver functions are normal.
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I am between 21 and 49 years old.
Exclusion Criteria
You may be eligible for the trial if you check “No” for criteria below:Select...
I am allergic to scopolamine or similar medications.
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I have a severe blockage in one nostril due to a deviated septum.
Select...
I am unable to give consent by myself.
Select...
I am currently using nasal spray medication.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 180 minutes
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~180 minutes
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
Side effects of intranasal scopolamine, as measured through a questionnaire with a subjective rating scale
Time to maximal concentration for scopolamine after intranasal administration (Tmax)
Secondary study objectives
Effectiveness in reducing motion sickness as measured by duration of chair ride.
Side effects data
From 2014 Phase 1 trial • 27 Patients • NCT0205133513%
Nausea
13%
Vision blurred
13%
Dizziness
9%
Dry mouth
9%
Oropharyngeal pain
100%
80%
60%
40%
20%
0%
Study treatment Arm
A: Placebo
B: Donepezil 10 mg
C: Roflumilast Dose A
D: Roflumilast Dose A + Donepezil 10 mg
Awards & Highlights
All Individual Drugs Already Approved
Therapies where all constituent drugs have already been approved are likely to have better-understood side effect profiles.
Trial Design
2Treatment groups
Experimental Treatment
Group I: PharmacokineticExperimental Treatment1 Intervention
Participants receive 1 dose of Scopolamine 0.4 mg delivered via a intranasal nebulizer developed by Creare LLC.
Group II: ChairExperimental Treatment2 Interventions
Participants receive 1 dose of Scopolamine 0.2 mg, 1 dose of Scopolamine 0.4 mg, and 1 dose of placebo saline delivered via the Creare LLC intranasal nebulizer. These dosages are all 1 week apart and the order is randomized.
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Scopolamine
FDA approved
Placebo
1995
Completed Phase 3
~2670
Research Highlights
Information in this section is not a recommendation. We encourage patients to speak with their healthcare team when evaluating any treatment decision.Mechanism Of Action
Side Effect Profile
Prior Approvals
Other Research
Common treatments for motion sickness often involve antihistamines and anticholinergics. Antihistamines, such as dimenhydrinate and meclizine, work by blocking histamine receptors in the brain that are involved in the vomiting reflex.
Anticholinergics, like scopolamine, inhibit the action of acetylcholine, a neurotransmitter that can trigger nausea and vomiting. The intranasal delivery method, as studied with intranasal nebulizers, enhances absorption through the nasal mucosa, providing faster onset of action and potentially more effective symptom relief.
This is particularly important for motion sickness patients who need quick and efficient relief to continue their activities without discomfort.
Effect of inhaling heated vapor on symptoms of the common cold.Effect of inhaling heated vapor on symptoms of the common cold.Heated, humidified air for the common cold.
Effect of inhaling heated vapor on symptoms of the common cold.Effect of inhaling heated vapor on symptoms of the common cold.Heated, humidified air for the common cold.
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Logistics
Participation is compensated
You will be compensated for participating in this trial.
Who is running the clinical trial?
Dartmouth-Hitchcock Medical CenterLead Sponsor
537 Previous Clinical Trials
2,540,023 Total Patients Enrolled
Jay C Buckey, Ph.DPrincipal InvestigatorDartmouth-Hitchcock Medical Center
Media Library
Eligibility Criteria:
This trial includes the following eligibility criteria:- I am allergic to scopolamine or similar medications.I have a significant condition like Crohn's, asthma, or glaucoma.I have not donated blood or had significant blood loss in the last 30 days., is required for all study participants
The study participants need to be in good health, as determined by their verbal medical history.I have not had major surgery in the last 3 months.I have not had nasal or sinus surgery in the last 90 days.I have wheezing or other breathing issues.I haven't had a cold, severe allergies, or sinus infections in the last month.I have a severe blockage in one nostril due to a deviated septum.I am unable to give consent by myself.My weight is normal for my height.I am currently using nasal spray medication.My kidney and liver functions are normal.I am between 21 and 49 years old.I am either male or female.
Research Study Groups:
This trial has the following groups:- Group 1: Chair
- Group 2: Pharmacokinetic
Awards:
This trial has 1 awards, including:- All Individual Drugs Already Approved - Therapies where all constituent drugs have already been approved are likely to have better-understood side effect profiles.
Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
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