ACTRN12618000294257已完成3 期
A double-blind randomised controlled study to evaluate the effectiveness of orallydosed Palmitoylethanolamide (PEA) compared to ibuprofen for reducing pain severityand duration of headaches in healthy participants aged 18 years and older.
试验速览
- 阶段
- 3 期
- 状态
- 已完成
- 入组人数
- 94
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomised controlled trial
- 主要目的
- Treatment
- 盲法
- Blinded (masking used)
入排标准
- 年龄范围
- 18 Years 至 o limit（—）
- 性别
- All
入选标准
- •Adults aged over 18
- •No history or evidence of clinically significant medical conditions including, but not
- •limited to, cardiovascular, neurological, psychiatric, renal, immunological, endocrine
- •(including uncontrolled diabetes or thyroid disease) or haematological abnormalities
- •that are uncontrolled.
- •Participant’s full agreement and ability to consent to participation in the study
- •At least 2 headache episodes per month
- •Access to a computer or smartphone for completing online questionnaires and
排除标准
- •Use of long-term medication (unless for controlled medical
- •condition as above)
- •Malignancy or treatment for malignancy within the previous 2 years
- •Pregnant or lactating women
- •Females not taking a prescribed form of contraception (i.e. oral
- •contraception pill, birth control implant e.g. implanon)
- •Chronic past and/or current alcohol use (>14 alcoholic drinks
- •Allergic or hypersensitive to any of the ingredients in the active or
- •ibuprofen formula
研究者
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