How 1988.
| Methods | Randomised, controlled trial comparing efficacy of transdermal scopolamine with placebo for preventing seasickness in both experienced and inexperienced sailors | |
| Participants | 122 officers and naval men who were either experienced (< 1 year in navy, n = 59) or inexperienced (< 1 year in navy, n = 63). Participant ages ranged from 19 to 45 years. | |
| Interventions | Transdermal Scopaderm TTS (1.5 mg scopolamine) or identical placebo patches applied 4 hours prior to sailing and then replaced every third day during sea voyage | |
| Outcomes | Subjective analogue scale measurement of degree of seasickness experienced during previous 24 hours at 8am every day | |
| Notes | No restrictions of food, water or other medications were imposed Schulz rating: randomisation B; allocation concealment B; selection bias B; blinding A |
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| Risk of bias | ||
| Bias | Authors' judgement | Support for judgement |
| Allocation concealment (selection bias) | Unclear risk | B ‐ Unclear |