ClinicalTrials.gg
Status unknownNCT01600911Updated May 18, 2012

Establish a Vegetable Signature Database From Human Metabolomics Responses

An interventional study of Low phytochemical diet(LPD), high phytochemical diet(HPD) in Human Metabolomic Responses to Plant Foods and Blood Pressure, sponsored by National Health Research Institutes, Taiwan. Status unknown at 1 site in Taiwan. Open to participants aged 18 Years to 60 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2012-05-18.

Sponsored by National Health Research Institutes, Taiwan · Not applicable, Interventional, and Treatment

The sponsor has not verified this record recently (last verified May 2012), so the status shown — last known as Active, not recruiting — may be out of date.
Phase
Not applicable
Study type
Interventional
Enrollment
50
Allocation
Not applicable
Ages
18 Years to 60 Years
Sex
All
01

Study summary

Vegetable is well known to prevent chronic disease,however, the mechanism of its nutrients and non-nutrients still remains to be discovered.We design a feeding study which provides plant foods to subjects one by another and monitoring metabolomic changes up to 7 hours.The goal of this study is to establish a protocol for documenting metabolomics response to plant foods and try to characterize plant foods in terms of their anti-hypertension potentials with metabolomic profiling information.

02

Conditions studied

  • Human Metabolomic Responses to Plant Foods
  • Blood Pressure

Keywords

  • metabolomics
  • nutri-metabolomics
  • plant food
  • blood pressure
03

In context

Lead sponsor

National Health Research Institutes, Taiwan is the lead sponsor of 127 studies on the registry; 29 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 60 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Age :18-60 years
  • Body Mass Index :18.5-30(kg/m2)
  • Non-smoking,alcohol abusing,and other bad hobbies

Exclusion criteria

Exclusion Criteria:

  • With regular drug intake e.g. anti-hypertensive or antidiabetes drug or history of immune, hepatic and metabolic disease or other unsuitable disorders e.g. cancer.
  • unwilling to stop regular food supplement e.g. vitamins, herb
  • cannot cooperate with designed diet
  • History of urinary tract infection or antibiotic use within the previous 3 month
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
50 participants (estimated)

Interventions

  • OtherLow phytochemical diet(LPD), high phytochemical diet(HPD)

    LPD is a basal diet which low in soy,vegetable and fruit and other plant food to approach low phytochemical. HPD is the diet which add two serving test vegetable in the lunch of LPD.

06

What researchers measure

Primary outcomes

  1. blood pressure

    fasting, before lunch,and every 1 hr after lunch

    Time frame: one day

Secondary outcomes

  1. metabolomic profile of serum and urine

    serum sample will be measure fasting ,before lunch,and every 1 hr after lunch;urine sample will be measure fasting ,before lunch(0hr),0-2 hr,2-4hr 4-7hr after lunch

    Time frame: one day

07

Study locations

1 site
  • National Health Research institues, Taiwan
    Miaoli County, Taiwan
08

Timeline

Tracking since Sep 25, 2026
Not marked actual or estimatedDates not marked actual or estimated

The record gives a start of Dec 2010, a primary completion of Dec 2013 and a completion of Dec 2013. It does not say whether these dates are actual or estimated.

How these figures are worked out, and which studies are left out of them.

Registered
May 16, 2012
First posted
May 17, 2012
Start
Dec 2010
Primary completionEst.
Dec 2013
CompletionEst.
Dec 2013
Last update
May 18, 2012
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on May 18, 2012, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT01600911
Collaborators
Tri-Service General Hospital (TSGH)
Responsible party
Sponsor
First posted
May 17, 2012
Start date
Dec 2010
Primary completion
Dec 2013 (estimated)
Completion
Dec 2013 (estimated)
Last update
May 18, 2012

Study contacts

Wen-Harn Pan, Ph.D.
principal investigator · National Health Research Institutes, Taiwan

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is status unknown, as verified in May 2012. You cannot join it, but the record below documents what was studied.

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