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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT02931006
Other study ID # Bovine Milk-HMO-CTIL
Secondary ID
Status Not yet recruiting
Phase N/A
First received September 15, 2016
Last updated October 10, 2016
Start date January 2017
Est. completion date January 2019

Study information

Verified date September 2016
Source Hadassah Medical Organization
Contact Ronit Kochman, MD
Phone 00 972 50 8946414
Email kochman.ronit@gmail.com
Is FDA regulated No
Health authority Israel: Ministry of Health
Study type Interventional

Clinical Trial Summary

50 men will be recruited to this study. Participants will be asked to ingest commercially available bovine milk. Hormonal profile will be analyzed before and after consumption.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 50
Est. completion date January 2019
Est. primary completion date January 2018
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Male
Age group 18 Years to 30 Years
Eligibility Inclusion Criteria:

- healthy, non infertile males

Exclusion Criteria:

- lactose intolerance

Study Design

Allocation: Randomized, Endpoint Classification: Bio-availability Study, Intervention Model: Parallel Assignment, Masking: Open Label


Related Conditions & MeSH terms

  • Gonadotrophin and Sex Hormone Changes

Intervention

Other:
water

bovine milk


Locations

Country Name City State
Israel Hadassah Medical Organization Jerusalem

Sponsors (2)

Lead Sponsor Collaborator
Hadassah Medical Organization Ministry of Health, Israel

Country where clinical trial is conducted

Israel, 

Outcome

Type Measure Description Time frame Safety issue
Primary sex hormone profile gonadotropin levels (Testosterone, Estradiol) 4 hours after consumption No