Status:
COMPLETED
Study to Assess Safety and Efficacy of Nephrosolid Tbs to Stimulate Urinary Output in Non-patient Volunteers
Lead Sponsor:
A. Vogel AG
Conditions:
Urine Specimen Collection
Eligibility:
All Genders
18-70 years
Phase:
PHASE3
Brief Summary
Fluid intake and urinary output are measured with /without intake of Nephrosolid tablets in acute ( 1 day application ) and chronic ( 28 days application) therapy.
Detailed Description
To evaluate safety and efficacy of Nephrosolid tbs in the stimulation of urinary output in healthy volunteers, all participants in this open-label study will be asked to record their fluid intake and ...
Eligibility Criteria
Inclusion
- Willingness and ability to record urine volume and fluid consumption over 3 days.
- Written consent to participate in the study.
Exclusion
- Disease or comprehension problems (language) that affect the accurate collection and measurement of urine levels over 3 days.
- Taking diuretic drugs, teas, herbal supplements, or systemic corticosteroids.
- Chronic nephropathy (such as glomerulonephritis, analgesic nephropathy, interstitial nephritis).
- Pregnancy or lactation.
- Psychiatric disorders that include suicidality.
- Surgical intervention in the 3 months prior to enrollment or scheduled surgery during the study.
- Known chronic diseases such as dementia, progressive systemic diseases.
- Known alcohol and/or drug addiction.
- Known allergies to goldenrod or birch leaves.
- Participation in one or more other clinical trials in the last 30 days
Key Trial Info
Start Date :
February 12 2018
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
January 31 2019
Estimated Enrollment :
66 Patients enrolled
Trial Details
Trial ID
NCT04338477
Start Date
February 12 2018
End Date
January 31 2019
Last Update
April 8 2020
Active Locations (2)
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1
Privat practice of Dr. med. Bruno Haug, Medizinisches Zentrum Arbon
Arbon, Thurgau, Switzerland, 9320
2
Private Practice Dr. med Bernhard Waelti
Freidorf, Thurgau, Switzerland, 9306