Primary Ovarian Insufficiency Clinical Trial
— OLIVAOfficial title:
in Vivo Activation of Ovarian Cortex in Premature Ovarian Insufficiency
Verified date | January 2017 |
Source | Hadassah Medical Organization |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
The OLIVA device will enable to perform shallow slashes on the ovarian cortex in patients undergoing oophorectomy. Prior to the resection of the ovary from the pedicle we will perform 5 parallel slashes 3 cm long. following oophorectomy investigation by the pathologist as to the depth of cuts and proximity to blood vessels and later.
Status | Not yet recruiting |
Enrollment | 30 |
Est. completion date | June 2018 |
Est. primary completion date | December 2017 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | Female |
Age group | 18 Years to 65 Years |
Eligibility |
Inclusion Criteria: - Peri/menopausal women undergoing laparoscopic oophorectomy Exclusion Criteria: - Women with ovarian malignancy - Women with polycystic ovarian syndrome |
Country | Name | City | State |
---|---|---|---|
n/a |
Lead Sponsor | Collaborator |
---|---|
Hadassah Medical Organization |
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Depth of cuts and closeness to blood vessel | The pathologist will measure the ovarian tissue after oophorectomy. The pathologist will assess whether the cuts into the cortex are superficial or penetrating the cortex into the medulla of the ovary. Another assessment is proximity of the cuts to ovarian vessels. The pathology report will aggregate the results of all measurements and will assess the safety of the OLIVA device | Up to 30 days after procedure | |
Secondary | Proximity of cuts to blood vessel | The pathologist will measure the ovarian tissue after oophorectomy. The pathologist will assess whether the cuts into the cortex are superficial or penetrating the cortex into the medulla of the ovary. Another assessment is proximity of the cuts to ovarian vessels. The pathology report will aggregate the results of all measurements and will assess the safety of the OLIVA device | Up to 30 days after procedure |
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