NCT01372852

Brief Summary

The objective of present study were to compare plasma adiponectin isoform status, their bioactivities newly diagnosed Chinese with healthy volunteer.

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
300

participants targeted

Target at P75+ for all trials

Timeline
Completed

Started May 2010

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

May 1, 2010

Completed
1.1 years until next milestone

First Submitted

Initial submission to the registry

June 11, 2011

Completed
3 days until next milestone

First Posted

Study publicly available on registry

June 14, 2011

Completed
4 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

October 1, 2011

Completed
2 months until next milestone

Study Completion

Last participant's last visit for all outcomes

December 1, 2011

Completed
Last Updated

June 14, 2011

Status Verified

May 1, 2010

Enrollment Period

1.4 years

First QC Date

June 11, 2011

Last Update Submit

June 13, 2011

Conditions

Keywords

Diabetes mellitus

Outcome Measures

Primary Outcomes (1)

  • plasma adiponectin concentration, isoform distribution and activity.

    participants will be followed for the duration of hospital stay, an expected average of 1 week

Study Arms (2)

T2DM patients

newly diagnosed T2DM patients and untreated with any drugs.

Non-diabetic Control Group

Eligibility Criteria

Age30 Years - 70 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodProbability Sample
Study Population

This study enrolls a group of 30-70years patients from primary care clinic who have diabetes history within 12 months and without taking any treatment.

You may qualify if:

  • Having a diabetic history within 12 months
  • BMI smaller than 30kg/m2

You may not qualify if:

  • Having any kinds of treatment affecting glucose
  • pregnant
  • uncontrolled hypertension, active cardiac disease, or other major liver, kidney disease

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Xijing Hospital

Xi'an, Shaanxi, 710032, China

RECRUITING

Biospecimen

Retention: SAMPLES WITHOUT DNA

blood,abdominal fat tissue

MeSH Terms

Conditions

Diabetes Mellitus

Condition Hierarchy (Ancestors)

Glucose Metabolism DisordersMetabolic DiseasesNutritional and Metabolic DiseasesEndocrine System Diseases

Study Officials

  • Ling Tao, M.D Ph.D

    Department of Cardiology of Xijing Hospital, Fourth Military Medical University

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Ling Tao, M.D Ph.D

CONTACT

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
CROSS SECTIONAL
Sponsor Type
OTHER

Study Record Dates

First Submitted

June 11, 2011

First Posted

June 14, 2011

Study Start

May 1, 2010

Primary Completion

October 1, 2011

Study Completion

December 1, 2011

Last Updated

June 14, 2011

Record last verified: 2010-05

Locations