NCT01255930

Brief Summary

The aim of this study is to evaluate placenta maturity by the sonographic textures.The evaluation of placenta maturity by the sonographic textures is related to anticipative pregnancy and actual pregnancy . By analyzing this theory, the investigators want to bring up another objective and accurate analysis method in order to provide information for the evaluation of clinical trials.

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 2010

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

January 1, 2010

Completed
11 months until next milestone

First Submitted

Initial submission to the registry

December 6, 2010

Completed
2 days until next milestone

First Posted

Study publicly available on registry

December 8, 2010

Completed
24 days until next milestone

Study Completion

Last participant's last visit for all outcomes

January 1, 2011

Completed
Last Updated

December 8, 2010

Status Verified

December 1, 2010

First QC Date

December 6, 2010

Last Update Submit

December 7, 2010

Conditions

Pregnant Women

Keywords

Pregnant WomenSonographic Textures

Eligibility Criteria

Age20 Years+
Sexfemale
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodProbability Sample
Study Population

pregnant women

You may qualify if:

  • pregnant women
  • Placenta Maturity by the Sonographic Textures

You may not qualify if:

  • intrauterine-growth retardation(IUGR)
  • Pre-eclampsia
  • Higher Blood Pressure
  • Fetal Distress during a labor

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Taipei Medical University-WanFang Hospital

Taipei, Taiwan

RECRUITING

Study Officials

  • Szu-Yuan Chou

    Taipei Medical University WanFang Hospital

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Szu-Yuan Chou

CONTACT

886-2-2930793098229@wanfang.gov.tw

Study Design

Study Type
observational
Observational Model
CASE ONLY
Time Perspective
RETROSPECTIVE
Sponsor Type
OTHER

Study Record Dates

First Submitted

December 6, 2010

First Posted

December 8, 2010

Study Start

January 1, 2010

Study Completion

January 1, 2011

Last Updated

December 8, 2010

Record last verified: 2010-12

Locations

TW(1)