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Measurement of Fibroid Volume and 2D, 3D US

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ClinicalTrials.gov Identifier: NCT02638688
Recruitment Status : Completed
First Posted : December 23, 2015
Last Update Posted : December 23, 2015
Sponsor:
Information provided by (Responsible Party):
Sherin A Shazly, Zagazig University

Study Description
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Brief Summary:
Objective: To compare 2-dimensional and 3-dimensional ultrasound measurements with the actual myomas volume after surgical removal, to clinically test the validity and usability of 3D ultrasound technology as opposed to conventional 2D real-time ultrasound and to assess the reliability of different ultrasound methods to measure volume of uterine fibroids.

Condition or disease Intervention/treatment
Gynecology Other: ultrasound

Study Design
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Study Type : Observational
Actual Enrollment : 3 participants
Observational Model: Case-Only
Time Perspective: Cross-Sectional
Official Title: Uterine Fibroid Volume After Myomectomy Compared to Pre-operative Measurement by Two and Three-dimensional Ultrasound
Study Start Date : September 2012
Actual Primary Completion Date : June 2015
Actual Study Completion Date : June 2015

Resource links provided by the National Library of Medicine

MedlinePlus related topics: Ultrasound

Groups and Cohorts
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Group/Cohort Intervention/treatment
2D ultrasound
2D-US measurements are the most accurate method for measuring fibroid volumes
 Other: ultrasound
3D ultrasound
3D-US measurements are the most accurate method for measuring fibroid volumes
 Other: ultrasound
postoperative
actual volume using change in water path measurements are the most accurate method for measuring fibroid volumes
 Other: ultrasound


Outcome Measures
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Primary Outcome Measures :
  1. measuring fibroid volumes [ Time Frame: 2012-2015 ]

Eligibility Criteria
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Information from the National Library of Medicine

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Ages Eligible for Study:   22 Years to 50 Years   (Adult)
Sexes Eligible for Study:   Female
Accepts Healthy Volunteers:   No
Sampling Method:   Probability Sample
Study Population
44
Criteria

Inclusion Criteria:

  • surgical intervention

Exclusion Criteria:

  • unfit for surgery
Contacts and Locations
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No Contacts or Locations Provided
More Information
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Top of Page Study Description Study Design Groups and Cohorts Outcome Measures Eligibility Criteria Contacts and Locations More Information
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Responsible Party: Sherin A Shazly, Faculty, Zagazig University
ClinicalTrials.gov Identifier: NCT02638688    
Other Study ID Numbers: s.shazly
2011 ( Registry Identifier: sherin )
First Posted: December 23, 2015    Key Record Dates
Last Update Posted: December 23, 2015
Last Verified: December 2015
Additional relevant MeSH terms:
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Leiomyoma
Neoplasms, Muscle Tissue
Neoplasms, Connective and Soft Tissue
Neoplasms by Histologic Type
Neoplasms