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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01031485
Other study ID # Valio-70
Secondary ID
Status Completed
Phase Phase 3
First received December 11, 2009
Last updated December 19, 2014
Start date January 2010
Est. completion date August 2010

Study information

Verified date December 2009
Source Valio Ltd
Contact n/a
Is FDA regulated No
Health authority Finland: Ethics Committee
Study type Interventional

Clinical Trial Summary

The purpose of this study is to investigate the effects of bioactive milk peptides on blood pressure in mildly hypertensive subjects.


Recruitment information / eligibility

Status Completed
Enrollment 0
Est. completion date August 2010
Est. primary completion date June 2010
Accepts healthy volunteers
Gender Both
Age group 30 Years to 60 Years
Eligibility Inclusion Criteria:

- age 30-60 years

- systolic blood pressure 140-160 mmHg and diastolic blood pressure 90-99 mmHg in office measurement

- apparently healthy

Exclusion Criteria:

- antihypertensive and lipid-lowering drugs

- unstable coronary artery disease, diabetes, malignant diseases, secondary hypertension

- BMI > 32 kg/m2

- milk allergy

- smoking

- alcohol abuse

- pregnancy, lactation

- simultaneous participation in other clinical trial

Study Design

Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Double-Blind


Related Conditions & MeSH terms


Intervention

Dietary Supplement:
Milk peptides and plant sterols

Other:
Placebo


Locations

Country Name City State
Finland Valio Ltd Helsinki Uusimaa

Sponsors (2)

Lead Sponsor Collaborator
Valio Ltd Helsinki University

Country where clinical trial is conducted

Finland, 

Outcome

Type Measure Description Time frame Safety issue
Primary Blood pressure
See also
  Status Clinical Trial Phase
Completed NCT01508026 - Study of the Efficacy and Safety of the Combination of Two FDA Approved Oral Medications, Nebivolol and Valsartan for Treatment of Stage 1 or 2 Hypertension Phase 3
Terminated NCT04402385 - Aspirin to Prevent Preeclampsia in Women With Elevated Blood Pressure and Stage 1 Hypertension (ASPPIRE) Phase 2