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Clinical Trial Details — Status: Withdrawn

Administrative data

NCT number NCT03507322
Other study ID # 1605-SEV-034-IR
Secondary ID
Status Withdrawn
Phase
First received
Last updated
Start date November 7, 2017
Est. completion date September 10, 2018

Study information

Verified date September 2018
Source IVI Sevilla
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

This study is focused on analysing the application of ultrasound scanning techniques as new biomarkers in reproductive medicine. Those biomarkers are based on the analysis of ultrasound texture in different areas of uterine tissue, using 2D/3D ultrasound scanning. Investigators will use the algorithm Text® to analyse the ultrasound texture of the endometrium and myometrium. The aim of the project is to study if it is possible to obtain measurable, objective and reproducible data in healthy volunteers which can be used to predict pregnancy and determine the best moment to perform embryo transfer in assisted reproductive technology (ART) cycles


Recruitment information / eligibility

Status Withdrawn
Enrollment 0
Est. completion date September 10, 2018
Est. primary completion date September 10, 2018
Accepts healthy volunteers No
Gender Female
Age group 18 Years to 49 Years
Eligibility Inclusion Criteria:

- Body mass index (BMI) between 18 and 30 kg/m2

- Not taking the contraceptive pill in a previous cycle

- Non-pregnant: beta human chorionic gonadotropin (HCG) test with negative result at the beginning of the study)

- No previous history of inflammatory diseases, circulatory diseases, abdomen or pelvic diseases

- Physical gynecological exploration without pathological findings

- Gynecological ultrasound study of the uterus with a normal result

Exclusion Criteria:

- Ultrasound studies with technical defects in image acquisition

- Simultaneous participation in other studies

- Previous participation in other study which can affect the results of the present study

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Ultrasound texturization
Along several visits to the clinic, the patients will be subjected to 2D/3D ultrasound scanning.

Locations

Country Name City State
Spain IVI Sevilla Sevilla

Sponsors (1)

Lead Sponsor Collaborator
IVI Sevilla

Country where clinical trial is conducted

Spain, 

Outcome

Type Measure Description Time frame Safety issue
Primary Clinical pregnancy rate Detection of gestational sac through ultrasound scanning indicating clinical pregnancy Around 5-6 weeks after embryo transfer
Primary Biochemical miscarriage rate Interruption of pregnancy after a positive result in the beta HCG test Up to one month after embryo transfer
Primary Clinical miscarriage rate Interruption of pregnancy after confirming clinical pregnancy using ultrasound scanning Up to 20 weeks after embryo transfer
Primary Chemical pregnancy rate Positive result in beta HCG test indicating pregnancy Around 14 days after embryo transfer
Primary beta HCG level Level of beta HCG in the test performed to detect pregnancy Around 14 days after embryo transfer
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