An Open Label Pilot Comparative Clinical Trial of Dehydroepiandrosterone (DHEA) Efficacy Administered as a Troche versus Oral Strips in Males with Adrenal Fatigue.

Medlab Clinical0 个研究点目标入组 30 人开始时间: 2016年8月5日最近更新: 2020年1月13日

适应症

试验速览

暂无简介。

•1) Male, > 18 years of age at time of entry on study
•2) Cognitive ability to understand informed consent process and to give informed consent to the experimental treatment
•3) Have been prescribed and taking DHEA for at least 6 months duration
•4) Participants agree to adhere to the study protocol
•5) Being treated for Adrenal Fatigue
•6) Symptoms are controlled with current hormone therapy
•7) BMI specification in the range of 15–30 kg/m2
•8) No history of malignant diseases

•1) Any clinically relevant abnormal findings which, in the opinion of the investigators / clinicians, may put the participant at risk of adverse events because of participation in the clinical trial including: physical examination, clinical chemistry, haematology, urinalysis, vital signs
•2) Taking dopaminergic or anti-dopaminergic medications, clonidine, psychotropic medications, narcotic analgesics, antihistamines used chronically
•3) The use of any dietary and herbal supplements including soy supplements
•4) The use of illicit drugs

发起方

Medlab Clinical