ISRCTN49884134已完成未知
aturopathic Treatment of Rotator Cuff Tendonitis Amongst Postal Workers, a randomized controlled parallel group study
适应症
试验速览
- 阶段
- 未知
- 状态
- 已完成
- 入组人数
- 85
研究概览
简要总结
2009 results in https://doi.org/10.1002/art.24675 (added 26/03/2021)
研究设计
- 研究类型
- Interventional
入排标准
- 性别
- All
入选标准
- •1. Males and females aged 18-65
- •2. Mentally competent subjects able to adhere to the given protocol and treatments administered as interventions
- •3. Self-selected candidates identifying themselves to suffer from pain in at least one shoulder for a period of 6 weeks or more
- •4. Normal on physical examination at the pre-study intake, and in the case of abnormalities the medical practitioner considers them to be clinically insignificant
- •5. Written and informed consent
- •6. The potential candidate must have a family doctor that they have seen in the last 12 months
- •7. A negative pregnancy test for menstruating women and a willingness to practice adequate birth control for the duration of the trial
- •8. Symptoms consistent with rotator cuff tendonitis, as determined by medical history or examination at screening
排除标准
- •1. Mentally or physically incapacitated such that informed consent cannot be obtained
- •2. Any history or other condition which the study physician regards as clinically significant to the study
- •3. A major illness considered to be clinically significant by the study physician within 3 months of the study start date
- •4. Current participation in another intervention trial
- •5. Pregnancy or intent to become pregnant in the next 6 months
- •6. Medication at doses that is contraindicated with supplement (specifically daily use of warfarin, high dose aspirin, other blood thinners, or antibiotics)
- •7. Current alcoholism or substance abuse
- •8. Current history of tumors
- •9. Any current serious disorders determined to be clinically significant to the study
- •10. Breast feeding women
- •11. No prior shoulder surgeries, or scheduled surgeries of any kind
- •12. Haemophiliac, suffering from severe liver damage, or suffering from any hemorrhagic disease
- •13. Major shoulder joint pathology on assessment including full tendon rupture or degenerative joint disease. In these cases, referral for further evaluation and diagnosis will occur
- •14. Subjects with known sensitivity to any ingredient in the test product or to any member of the Bromeliaceae family, including pineapple
- •15. Subjects using Natural Health Products (NHPs) for 2 weeks prior to enrolment which affect shoulder pain or inflammation, contain phlogenzym or therapeutic constituents of the diet in supplement form
- •16. Current use of corticosteroid injection therapy
研究者
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