NCT00420446

Brief Summary

The purpose of the project is to elucidate the effect on blood pressure by daily intake of dairy products. Previous studies have demonstrated a beneficial effect on blood pressure. In total 90 subjects will be enrolled. For eight weeks, the participants will ingest one of two different dairy produces. Before, during and after the study period, the blood pressure is measured.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Timeline
Completed

Started Jan 2007

Shorter than P25 for not_applicable hypertension

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

January 1, 2007

Completed
9 days until next milestone

First Submitted

Initial submission to the registry

January 10, 2007

Completed
1 day until next milestone

First Posted

Study publicly available on registry

January 11, 2007

Completed
6 months until next milestone

Study Completion

Last participant's last visit for all outcomes

July 1, 2007

Completed
Last Updated

July 27, 2007

Status Verified

February 1, 2007

First QC Date

January 10, 2007

Last Update Submit

July 25, 2007

Conditions

Hypertension

Interventions

Adjusted dietBEHAVIORAL

Eligibility Criteria

Age18 Years - 70 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • Borderline hypertension

You may not qualify if:

  • CVD, Diabetes, any kind of antihypertensive therapy.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Department of clinical physiology, Glostrup Hospital

Glostrup Municipality, 2600, Denmark

Location

MeSH Terms

Conditions

Hypertension

Condition Hierarchy (Ancestors)

Vascular DiseasesCardiovascular Diseases

Study Officials

  • Lars T Jensen, M.D., Ph

    Department of Clinical Physiology, Glostrup Hospital, DK-2600 Glostrup, Denmark

    PRINCIPAL INVESTIGATOR

  • Hans Ibsen, M.D., D.M.Sc

    Department of Internal Medicine M, Glostrup Hospital, DK-2600 Glostrup, Denmark

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
DOUBLE
Intervention Model
PARALLEL
Sponsor Type
OTHER

Study Record Dates

First Submitted

January 10, 2007

First Posted

January 11, 2007

Study Start

January 1, 2007

Study Completion

July 1, 2007

Last Updated

July 27, 2007

Record last verified: 2007-02

Locations

DK(1)