Working…
COVID-19 is an emerging, rapidly evolving situation.
Get the latest public health information from CDC: https://www.coronavirus.gov.

Get the latest research information from NIH: https://www.nih.gov/coronavirus.
ClinicalTrials.gov
ClinicalTrials.gov Menu

Evaluation of Placenta Maturity by the Sonographic Textures

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
 
ClinicalTrials.gov Identifier: NCT01255930
Recruitment Status : Unknown
Verified December 2010 by Taipei Medical University WanFang Hospital.
Recruitment status was:  Recruiting
First Posted : December 8, 2010
Last Update Posted : December 8, 2010
Sponsor:
Information provided by:
Taipei Medical University WanFang Hospital

Tracking Information
First Submitted Date December 6, 2010
First Posted Date December 8, 2010
Last Update Posted Date December 8, 2010
Study Start Date January 2010
Primary Completion Date Not Provided
Current Primary Outcome Measures Not Provided
Original Primary Outcome Measures Not Provided
Change History No Changes Posted
Current Secondary Outcome Measures Not Provided
Original Secondary Outcome Measures Not Provided
Current Other Pre-specified Outcome Measures Not Provided
Original Other Pre-specified Outcome Measures Not Provided
 
Descriptive Information
Brief Title Evaluation of Placenta Maturity by the Sonographic Textures
Official Title Evaluation of Placenta Maturity by the Sonographic Textures
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.
Detailed Description Not Provided
Study Type Observational
Study Design Observational Model: Case-Only
Time Perspective: Retrospective
Target Follow-Up Duration Not Provided
Biospecimen Not Provided
Sampling Method Probability Sample
Study Population pregnant women
Condition Pregnant Women
Intervention Not Provided
Study Groups/Cohorts Not Provided
Publications * Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Recruitment Information
Recruitment Status Unknown status
Estimated Enrollment
 (submitted: December¬†7,¬†2010)
150
Original Estimated Enrollment Same as current
Estimated Study Completion Date January 2011
Primary Completion Date Not Provided
Eligibility Criteria

Inclusion Criteria:

  • pregnant women
  • Placenta Maturity by the Sonographic Textures

Exclusion Criteria:

  • intrauterine-growth retardation(IUGR)
  • Pre-eclampsia
  • Higher Blood Pressure
  • Fetal Distress during a labor
Sex/Gender
Sexes Eligible for Study: Female
Ages 20 Years and older   (Adult, Older Adult)
Accepts Healthy Volunteers No
Contacts Contact information is only displayed when the study is recruiting subjects
Listed Location Countries Taiwan
Removed Location Countries  
 
Administrative Information
NCT Number NCT01255930
Other Study ID Numbers 99016
Has Data Monitoring Committee No
U.S. FDA-regulated Product Not Provided
IPD Sharing Statement Not Provided
Responsible Party Szu-Yuan Chou, Obsterics & Gynecology
Study Sponsor Taipei Medical University WanFang Hospital
Collaborators Not Provided
Investigators
Principal Investigator: Szu-Yuan Chou Taipei Medical University WanFang Hospital
PRS Account Taipei Medical University WanFang Hospital
Verification Date December 2010