- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03382002
Association Between Oxidative Parameters in Fertilization Medium of Cumulus Oocyte Complex and Outcome in IVF
January 31, 2019 updated by: Zofnat Wiener, Carmel Medical Center
Evaluation of Association Between Oxidative Parameters in Fertilization Medium of Cumulus Oocyte Complex (COC( as Measured by the TCL Assay and Clinical and Laboratory Outcome Parameters in IVF
Medium of cumulus-oocyte complex will be assessed for oxidative status.
Study Overview
Study Type
Observational
Enrollment (Anticipated)
322
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
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-
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Haifa, Israel
- Recruiting
- Carmel Medical Center
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Contact:
- Zofnat Wiener, MD
- Phone Number: 97248250335
- Email: wiener_zofnat@clalit.org.il
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Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years to 45 years (Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
Female
Sampling Method
Non-Probability Sample
Study Population
Patients undergoing in vitro fertilization
Description
Inclusion Criteria:
•Patients undergoing in vitro fertilization treatment
Exclusion Criteria:
•Patients undergoing intracytoplasmic sperm injection
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Association of parameters of oxidative state with cycle outcome (pregnancy: yes/no)
Time Frame: two years
|
The oxidative status in the incubation medium of the cumulus-oocyte complex will be assessed looking for an association between oxidative parameters and cycle outcome (pregnancy: yes/no))
|
two years
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
November 28, 2017
Primary Completion (Anticipated)
November 28, 2019
Study Completion (Anticipated)
April 28, 2020
Study Registration Dates
First Submitted
November 29, 2017
First Submitted That Met QC Criteria
December 21, 2017
First Posted (Actual)
December 22, 2017
Study Record Updates
Last Update Posted (Actual)
February 1, 2019
Last Update Submitted That Met QC Criteria
January 31, 2019
Last Verified
January 1, 2019
More Information
Terms related to this study
Other Study ID Numbers
- CarmelMC
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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