NCT00487955

Brief Summary

The purpose of our study is to evaluate the metabolic contribution of the human microbiota to resting energy expenditure

Trial Health

43
At Risk

Trial Health Score

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

Trial has exceeded expected completion date
Enrollment
40

participants targeted

Target at P25-P50 for all trials

Timeline
Completed

Started Jun 2007

Shorter than P25 for all trials

Geographic Reach
1 country

1 active site

Status
unknown

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

June 1, 2007

Completed
17 days until next milestone

First Submitted

Initial submission to the registry

June 18, 2007

Completed
1 day until next milestone

First Posted

Study publicly available on registry

June 19, 2007

Completed
6 months until next milestone

Study Completion

Last participant's last visit for all outcomes

December 1, 2007

Completed
Last Updated

June 19, 2007

Status Verified

March 1, 2007

First QC Date

June 18, 2007

Last Update Submit

June 18, 2007

Conditions

Gastritis

Keywords

gastritishelicobacter pyloriREEpatients with gastritis that refers to helicobacter pylori treatment

Interventions

Resting Energy Expenditure examinationPROCEDURE

Eligibility Criteria

Age20 Years - 60 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64)

You may qualify if:

  • patients that refers to helicobacter pylori treatment
  • Aged 20-60 years old
  • Kg/m2 ≤ BMI ≤ 30 Kg/m2
  • Functional GI trace with permanent stool number
  • Keeping on a permanent diet
  • Written informed consent
  • Stated availability throughout the study period
  • Mental ability to understand and follow the protocol

You may not qualify if:

  • Use of laxatives
  • Confirmed GI tract infections or inflammatory bowel disease
  • Any major chronic illness
  • Pregnancy
  • Participation in other clinical trials
  • Use of oral or intravenous antibiotics during 8 weeks prior to recruitment

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

The Unit of Clinical Nutrition

Tel Aviv, Israel

RECRUITING

MeSH Terms

Conditions

Gastritis

Condition Hierarchy (Ancestors)

GastroenteritisGastrointestinal DiseasesDigestive System DiseasesStomach Diseases

Study Officials

  • Nachum Vaisman, Prof.

    STUDY DIRECTOR

Central Study Contacts

Nachum Vaisman, Prof.

CONTACT

+972-524-266-596vaisman@tasmc.health.gov.il

Aharon Halak, Dr.

CONTACT

+972-522-311-929efratmo@tasmc.health.gov.il

Study Design

Study Type
observational
Observational Model
DEFINED POPULATION
Time Perspective
OTHER
Sponsor Type
OTHER GOV

Study Record Dates

First Submitted

June 18, 2007

First Posted

June 19, 2007

Study Start

June 1, 2007

Study Completion

December 1, 2007

Last Updated

June 19, 2007

Record last verified: 2007-03

Locations

IL(1)