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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT01198106
Other study ID # 792-2008-IDF-CTIL
Secondary ID
Status Recruiting
Phase N/A
First received September 8, 2010
Last updated September 8, 2010
Start date September 2009
Est. completion date September 2010

Study information

Verified date September 2010
Source Medical Corps, Israel Defense Force
Contact Amit Assa, Dr.
Phone 03-7379142
Is FDA regulated No
Health authority Israel: Israeli Health Ministry Pharmaceutical Administration
Study type Interventional

Clinical Trial Summary

BACKGROUND:flight simulator have become an important component in pilot training. However, they are known to be associated with motion sickness like symptoms defined as Simulator Sickness (SS). Prevention countermeasures against motion sickness have been studied extensively focusing on cholinergic blockers and antihistamines. Most comparataive studies emphasized the effectiveness of scopolamine over outher agents. Evidence, though, on prophylaxis against SS is sparse.

OBJECTIVE: to assess the effectiveness of oral scopolamine versus oral cinnarizine or placebo for SS prevention in helicopter pilots.

DESIGN: a prospective, placebo controlled double-blind.

SETTING: Israel Air Forse (IAF) Helicopter Aircaft vWeapon System Trainer.

PARTICIPANTS: IAF experienced helicopter pilots.

INTERVENTION: 0.6 mg oral scopolamine or 50 mg oral cinnarizine or placebo 1 hour before beginning of a 3 sortie simulator training


Recruitment information / eligibility

Status Recruiting
Enrollment 100
Est. completion date September 2010
Est. primary completion date September 2010
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 21 Years to 50 Years
Eligibility Inclusion Criteria:

- age 21 to 50 years, qualified helicopter pilots

- history of average TS score in SSQ more than 7.48

Exclusion Criteria:

- known vestibular, visual or central nervous system pathology

- fever of more than 37.2 degrees

- any MS like symptom prior to simulator training

- any compromising acute health problem

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Crossover Assignment, Masking: Single Blind (Subject), Primary Purpose: Prevention


Related Conditions & MeSH terms


Intervention

Drug:
scopolamine
0.6 mg
cinnarizine
50 mg

Locations

Country Name City State
Israel base 30 IAF Yavne

Sponsors (1)

Lead Sponsor Collaborator
Medical Corps, Israel Defense Force

Country where clinical trial is conducted

Israel, 

Outcome

Type Measure Description Time frame Safety issue
Primary Finding more effective treatment to the motion sickness symptoms during and after simulator training. To record a significant difference in motion sickness symptoms reduction during and after simulator training, after taking cinnarizine, scopolamine or placebo. We predict that scopolamine will prove to be more effective than cinnarizine with fewer side effects that can compromise pilot's performance during training. 1 year Yes
See also
  Status Clinical Trial Phase
Completed NCT02122354 - Triggers and Responses to Simulator Sickness in Videogame Players N/A