ACTRN12616000741482Completed未知
A randomised placebo controlled clinical trial on the efficacy of Caralluma supplement for anxiety and stress in healthy adults over eight weeks
Conditions
Trial Snapshot
- Phase
- 未知
- Status
- Completed
- Sponsor
- RDC Global
- Enrollment
- 117
Study Overview
Brief Summary
No summary available.
Study Design
- Study Type
- Interventional
- Allocation
- Randomised controlled trial
- Primary Purpose
- Treatment
- Masking
- Blinded (masking used)
Eligibility Criteria
- Ages
- 18 Years to 75 Years (—)
- Sex
- All
Inclusion Criteria
- •Participants will be included for assessment if they self-report mild-moderate anxiety (BAI >9<30), are not diagnosed with depression or a mood disorder, are otherwise healthy, and have given written informed consent.
Exclusion Criteria
- •Participants will be excluded if they:
- •have a known hypersensitivity to herbal drugs, or nutritional supplements;
- •have been diagnosed with hypertension and are receiving medication;
- •have a medical condition which, in the opinion of the investigator, makes them unsuitable or deemed unhealthy (including a BMI > 30);
- •have currently or have a history of chronic alcohol and/or drug abuse;
- •have participated in any other clinical trial during last 30 days;
- •are currently participating in another clinical trial;
- •have been diagnosed with a mood disorder;
- •have minimal or severe anxiety on the Beck Anxiety Inventory (<10, or > 29);
- •suffered severe PMS with mood or pain that would change during the study;
- •suffered from any neurological disorder;
- •are taking supplements that impact mood or appetite (e.g., St John’s Wort, leptin);
- •are already taking Caralluma.
Investigators
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