NCT00800631

Brief Summary

The development and severity of sepsis induced myocardial dysfunction can be monitored from the serum biomarker.

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
150

participants targeted

Target at P50-P75 for all trials

Timeline
Completed

Started Jan 2008

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

January 1, 2008

Completed
11 months until next milestone

First Submitted

Initial submission to the registry

December 1, 2008

Completed
1 day until next milestone

First Posted

Study publicly available on registry

December 2, 2008

Completed
1 month until next milestone

Primary Completion

Last participant's last visit for primary outcome

January 1, 2009

Completed
11 months until next milestone

Study Completion

Last participant's last visit for all outcomes

December 1, 2009

Completed
Last Updated

December 2, 2008

Status Verified

December 1, 2008

Enrollment Period

1 year

First QC Date

December 1, 2008

Last Update Submit

December 1, 2008

Conditions

Sepsis

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodProbability Sample
Study Population

sepsis

You may qualify if:

  • Sepsis patients with 2 of the followings when arrival ER and treated \> 6 hours:
  • BT \>38℃ or\<36℃
  • HR \>90/min
  • RR \>20/min or PaCO2 \< 32 mmHg
  • WBC count \>12×109/L or \<4×109/L or immature form \>10％

You may not qualify if:

  • Age \< 18
  • Major trauma patients
  • Pregnancy
  • Willing to do not aggressive treatment

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

ER of National Taiwan Univeristy Hospital

Taipei, 100, Taiwan

RECRUITING

MeSH Terms

Conditions

Sepsis

Condition Hierarchy (Ancestors)

InfectionsSystemic Inflammatory Response SyndromeInflammationPathologic ProcessesPathological Conditions, Signs and Symptoms

Central Study Contacts

ChiungYuan Hsu, Mph

CONTACT

886-2-23123456dtemer01@gmail.com

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER

Study Record Dates

First Submitted

December 1, 2008

First Posted

December 2, 2008

Study Start

January 1, 2008

Primary Completion

January 1, 2009

Study Completion

December 1, 2009

Last Updated

December 2, 2008

Record last verified: 2008-12

Locations

TW(1)