Healia Clinical Trials Information Database

An Intervention Program to Control Diabetes

Study to evaluate the effectiveness of a structured intervention to improve diabetes control.

Status: Completed (Phase 4). Started on May 1st, 2005.

Enrollment: 150 subjects

Study Type: Interventional

Study Design:

  • Treatment
  • Randomized
  • Open Label
  • Active Control
  • Parallel Assignment
  • Efficacy Study

Conditions:

Interventions:

  • Other: daily enteral nutritional product and/or behavioral changes

Eligibility

Inclusion Criteria:

  • informed consent

  • 18-70 adults

  • Type 2 Diabetes

  • Males and non-pregnant females

Exclusion Criteria:

  • Use of exogenous insulin for glucose control

  • Use of medications or supplements for weight loss

  • Advanced diabetes complications

  • Recent history of cardiovascular event

Gender

Both

Mininum Age

18 Years

Maximum Age

70 Years


Resources

Source: Abbott Nutrition

Authority: China: Ethics Committee

Locations

  • Huandong Hospital
    Shanghai
    China

Officials

  • Jianqin Sun, MD, MPH (Principal Investigator, Clinical Nutrition Center, Huadong Hospital)

Sponsors

  • Abbott Nutrition (Lead Sponsor)

References

None.

Links

None.


Date Verified
October 1st, 2007
First Received
October 12th, 2007
Last Changed
October 12th, 2007

Information obtained from ClinicalTrials.gov on July 15, 2008. Link to the current ClinicalTrials.gov record.


All data in the Healia Clinical Trials Information Database and content displayed by the Healia Clinical Trials Search Engine are licensed from the National Institutes of Health (National Library of Medicine), which collects and maintains the data.

The Healia Clinical Trials Search Engine searches the data set at clinicaltrials.gov, providing up-to-date information about current clinical trials. In the Healia Clinical Trials Database you can find information on new experimental drugs, medical devices, and other types of treatments for all types of diseases. Each clinical trial description includes information about the phase of the trial (phase I, phase II, or phase III), the trial’s methods, such as whether it is a randomized, placebo controlled, double blind study, and the status of the trial including whether or not the trial is currently enrolling new participants.


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