The Efficacy Study of FUROSAP: A Testosterone Booster Supplement In Humans.
Efficacy Evaluation of Furosap, a Testosterone Booster Supplement in Human Volunteers : An add-on Study
1 other identifier
interventional
100
1 country
1
Brief Summary
The study evaluates the effect of Fenugreek seed extract (Furosap) in management of symptomatic hypogonadism as fenugreek seed extract is a testosterone booster. Fenugreek seeds extract are known to possess protodioscin and the extract is reported to improve sperm count, sperm morphology and protective effect on male reproductive system. All the participants will receive one capsule (500 mg) of furosap once a day.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for not_applicable
Started Feb 2014
Typical duration for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
February 1, 2014
CompletedFirst Submitted
Initial submission to the registry
September 29, 2015
CompletedFirst Posted
Study publicly available on registry
March 9, 2016
CompletedPrimary Completion
Last participant's last visit for primary outcome
March 1, 2017
CompletedStudy Completion
Last participant's last visit for all outcomes
March 1, 2017
CompletedSeptember 15, 2017
May 1, 2017
3.1 years
September 29, 2015
September 14, 2017
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
% Change in serum Testosterone levels
12 weeks
Secondary Outcomes (1)
% improvement in sperm count
12 weeks
Study Arms (1)
Fenugreek seeds extract 500 mg
OTHERFenugreek seeds extract ( Furosap) one caps once a day
Interventions
Furosap one caps OD
Eligibility Criteria
You may qualify if:
- Agrees to written as well as audio-visual informed consent.
- Ability to understand the risks/benefits of the protocol
- Male between 35-65 years of age.
- Diagnosed with Symptomatic hypogonadism
You may not qualify if:
- Uncooperative Subjects
- Impaired hepatic function indicated by SGOT/SGPT \>2.5 times the upper limit of normal.
- Abnormal liver or kidney function tests (ALT or AST \> 2 times the upper limit of normal; elevated creatinine, males \> 125 µmol/L or 1.4mg/dl, females \> 110 µmol/L or1.2mg/dl)
- Patients suffering from CAD
- History of malignancy
- History of hypersensitivity to any of the investigational drugs
- Receiving any other testosterone booster therapy/medication/supplement within the last 2 months
- History of coagulopathies
- High alcohol intake (\>2 standard drinks per day)
- History of psychiatric disorder that may impair the ability of subjects to provide written informed consent.
- Any medical condition, where the investigator feels participation in the study could be detrimental to the subjects overall well-being.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Department of Urology, King George's Medical University, Lucknow, UP, India
Lucknow, Uttar Pradesh, 226003, India
Related Publications (4)
Steels E, Rao A, Vitetta L. Physiological aspects of male libido enhanced by standardized Trigonella foenum-graecum extract and mineral formulation. Phytother Res. 2011 Sep;25(9):1294-300. doi: 10.1002/ptr.3360. Epub 2011 Feb 10.
PMID: 21312304BACKGROUNDAswar U, Bodhankar SL, Mohan V, Thakurdesai PA. Effect of furostanol glycosides from Trigonella foenum-graecum on the reproductive system of male albino rats. Phytother Res. 2010 Oct;24(10):1482-8. doi: 10.1002/ptr.3129.
PMID: 20878698BACKGROUNDHamden K, Jaouadi B, Carreau S, Aouidet A, El-Fazaa S, Gharbi N, Elfeki A. Potential protective effect on key steroidogenesis and metabolic enzymes and sperm abnormalities by fenugreek steroids in testis and epididymis of surviving diabetic rats. Arch Physiol Biochem. 2010 Jul;116(3):146-55. doi: 10.3109/13813455.2010.486405.
PMID: 20507258BACKGROUNDGauthaman K, Ganesan AP, Prasad RN. Sexual effects of puncturevine (Tribulus terrestris) extract (protodioscin): an evaluation using a rat model. J Altern Complement Med. 2003 Apr;9(2):257-65. doi: 10.1089/10755530360623374.
PMID: 12804079BACKGROUND
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Dr. Satyanarayan sankhwar, M.S., M.Ch.
King George's Medical University, Lucknow, UP, India
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- NA
- Masking
- NONE
- Purpose
- SUPPORTIVE CARE
- Intervention Model
- SINGLE GROUP
- Sponsor Type
- INDUSTRY
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
September 29, 2015
First Posted
March 9, 2016
Study Start
February 1, 2014
Primary Completion
March 1, 2017
Study Completion
March 1, 2017
Last Updated
September 15, 2017
Record last verified: 2017-05
Data Sharing
- IPD Sharing
- Will not share