NCT01261195

Brief Summary

HUVEC primary cells for researches about the relation between plasma leakage and infections.

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
60

participants targeted

Target at P25-P50 for all trials

Timeline
Completed

Started Mar 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

March 1, 2010

Completed
10 months until next milestone

First Submitted

Initial submission to the registry

December 14, 2010

Completed
2 days until next milestone

First Posted

Study publicly available on registry

December 16, 2010

Completed
12 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 1, 2011

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

December 1, 2011

Completed
Last Updated

August 17, 2011

Status Verified

June 1, 2011

Enrollment Period

1.8 years

First QC Date

December 14, 2010

Last Update Submit

August 16, 2011

Conditions

Eligibility Criteria

Sexfemale
Healthy VolunteersYes
Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

healthy pregnant women

You may qualify if:

  • healthy pregnant women
  • would like to join this study

You may not qualify if:

  • venereal disease

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Kaohsiung Medical University Chung-Ho Memorial Hospital

Kaohsiung City, Kaohsiung, 807, Taiwan

RECRUITING

Biospecimen

Retention: SAMPLES WITH DNA

the umbilical cord

Study Officials

  • Jih-Jin Tsai, Doctor

    KMUH Tropical Medicine Center

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Jessie Jou, Assistant

CONTACT

Study Design

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

Study Record Dates

First Submitted

December 14, 2010

First Posted

December 16, 2010

Study Start

March 1, 2010

Primary Completion

December 1, 2011

Study Completion

December 1, 2011

Last Updated

August 17, 2011

Record last verified: 2011-06

Locations