- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01977664
In Vitro Maturation Induction of Oocytes From a Woman With Syndrome of Repeated Oocyte Maturation Failure in Vitro
November 6, 2013 updated by: Yang Jie, The Second Affiliated Hospital of Kunming Medical University
The Factors Primarily Intrinsic to the Oocyte Are Responsible to the Oocyte Maturation Defective: a Case Report.
Donated oocytes is from a patient with repeated oocyte maturation failure in IVF cycles.
Cytoplasm of matured metaphase II oocyte and active MPF were injected into the donated oocytes.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
The study reported a woman with syndrome of repeated oocyte maturation failure where there is repeated production of immature oocytes.She underwent two IVF cycles in other hospital.
All oocytes obtained were immature and the treatment were stopped.She underwent her third try in our hospital.
The couple gave their informed consent: ICSI will be performed if maturation occurred, otherwise, the treatment would be stopped and the oocytes would be donated for study if the oocytes were not matured after 24 hours of culture.
After ovarian hyperstimulation,14 oocytes were obtained.
None of them was matured.
The cycle was canceled and the oocytes were donated for study.To induce the immature oocytes in vitro, oocytes were 1)cultured in follicular fluid containing matured metaphase II oocyte; 2) performed intracytoplasmic sperm injection (ICSI) to induce intracellular Ca2+]i oscillations; 3)injected with active maturation promoting factor (MPF), 4)injected with cytoplasm of matured metaphase II oocyte.
Study Type
Observational
Enrollment (Actual)
1
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
-
-
Yunnan
-
Kunming, Yunnan, China, 650101
- The Second Affiliated Hospital of Kunming Medical University
-
-
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
32 years to 32 years (Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
Female
Sampling Method
Non-Probability Sample
Study Population
a patient with repeated oocyte maturation failure in IVF cycles
Description
Inclusion Criteria:
Clinical diagnosis of syndrome of repeated oocyte maturation
Exclusion Criteria:
patients with matured oocytes in IVF cycles
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
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
---|---|
oocyte maturation failure
no intervention
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
Oocyte nucleus maturation
Time Frame: April,2012
|
April,2012
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Principal Investigator: Jie Yang, M.Sc, The Second Affiliated Hospital of Kunming Medical University
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
March 1, 2012
Primary Completion (Actual)
April 1, 2012
Study Completion (Actual)
April 1, 2012
Study Registration Dates
First Submitted
October 9, 2013
First Submitted That Met QC Criteria
November 6, 2013
First Posted (Estimate)
November 7, 2013
Study Record Updates
Last Update Posted (Estimate)
November 7, 2013
Last Update Submitted That Met QC Criteria
November 6, 2013
Last Verified
October 1, 2013
More Information
Terms related to this study
Other Study ID Numbers
- 201301
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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