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The study was stopped prematurely due to low recruitment rate
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| Name | Class |
|---|---|
| Eugonia IVF Unit, Athens, Greece | OTHER |
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Oocyte quality is a basic parameter that affects embryo quality and therefore it influences the outcome of assisted reproduction. It has been suggested that oocyte quality is improved by the intake of vitamins and antioxidants.
Ova-Max is a dietary supplement that consists of vitamins, minerals and antioxidants which improve women's oocytes by preventing oxidative stress. Specifically, Ovamax includes Chasteberry, Melatonin, Myo-Inositol, Folic Acid, Co-Enzyme Q10, Vitamin E, L-Arginine, Grape seed extract and Alpha-lipoic Acid. The purpose of this study is to evaluate the influence of Ova-max intake on oocyte quality in women undergoing In Vitro Fertilization.
According to the research hypothesis the administration of Ova-Max for three months increases oocyte quality in women undergoing intracellular sperm injection after ovarian stimulation and oocyte retrieval.
Randomisation
This study is a blind randomized control trial to evaluate the association between Ova-Max intake and the quality of oocytes retrieved after ovarian stimulation. Randomization will be performed at least three months prior to initiation of treatment and patients will be assigned to either Ova-max or placebo by a computer-generated randomization list.
Ovarian Stimulation
A standard ovarian stimulation protocol for all patients will be followed with 200-300 IU of recombinant FSH and GnRH antagonist starting on day 5 of stimulation.
Induction of final oocyte maturation will be performed by recombinant hCG or GnRH agonist. Women who are planned for fresh embryo transfer, will be administered subcutaneous progesterone for luteal phase support starting on the day of oocyte retrieval.
Oocyte Quality Assessment
After oocyte retrieval the cumulus cells of the Cumulus Oocyte complex (COC) are removed and quality of all mature, metaphase II (MII) oocytes is assessed according to the following parameters:
Each parameter is graded as worst (-1), average (0), or best (1) and a total oocyte score (TOS) is calculated by summing up individual parameter assessments.
The maximal TOS of an oocyte, therefore, could be +6, the lowest -6.
The 6 individual parameters are assessed in detail as follows:
After having assessed the TOS of all MII oocytes, the Mean Oocyte Score (MOS) of the patient is calculated by dividing the sum of all TOS of the patient by the number of her oocytes.
Statistical analysis
Group sample sizes of 79 and 79 achieve 80% power to detect a difference of -1.0 between the null hypothesis that both group TOS means are -1.1 and the alternative hypothesis that the mean TOS of the Ova-Max group is -0.1, with known group standard deviations of 2.2 and 2.2 and with a significance level (alpha) of 0.05000 using a two-sided Mann-Whitney test assuming that the actual distribution is uniform
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Ova-max | Active Comparator | antioxidant, dietary supplement |
|
| Placebo | Placebo Comparator | placebo |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Ova-max | Other | use Ova-max 3 months prior to treatment initiation |
| |
| Measure | Description | Time Frame |
|---|---|---|
| Mean oocyte score | The sum of the total oocyte scores of the patient divided by the number of her oocytes. Oocytes is assessed according to the following parameters:
Each parameter is graded as worst (-1), average (0), or best (1) and a total oocyte score (TOS) is calculated by summing up individual parameter assessments. The maximal TOS of an oocyte, therefore, could be +6, the lowest -6. | 1-3 hours after oocyte retrieval |
| Measure | Description | Time Frame |
|---|---|---|
| Percentage of mature oocytes | number of mature oocytes of a woman divided by her total oocyte number | 2-4 hours after oocyte retrieval |
| Percentage of fertilised oocytes | number of oocytes of a woman that are fertilised divided by the total oocyte injected with sperm |
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Inclusion Criteria:
Exclusion criteria:
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| Name | Affiliation | Role |
|---|---|---|
| Efstratios M Kolibianakis, Professor | Aristotle University Thessaloniki | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Papageorgiou Hospital | Thessaloniki | Central Macedonia | 54631 | Greece |
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| Type | Date | Date Unknown |
|---|---|---|
| Release | Jan 22, 2026 | |
| Reset | Feb 9, 2026 |
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| Release Date | Unrelease Date | Unrelease Date Unknown | Reset Date | MCP Release Number |
|---|---|---|---|---|
| Jan 22, 2026 | Feb 9, 2026 | |||
| Jun 28, 2026 |
| ID | Term |
|---|---|
| D007246 | Infertility |
| C565840 | Long Qt Syndrome 3 |
| ID | Term |
|---|---|
| D000091662 | Genital Diseases |
| D000091642 | Urogenital Diseases |
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randomised controlled trial
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use of placebo, masked randomisation list
| placebo |
| Other |
use placebo 3 months prior to treatment initiation |
|
| 16-18 hours after fertilisation |
| Blastulation rate | the number of embryos that have reached blastocyst stage divided by the number of fertilised oocytes | day 5 after fertilisation |
| Pregnancy rate | the number of women who got pregnant divided by the number of women who underwent embryo transfer | 6 weeks after embryo transfer |
| Total number of COCs collected | total number of cumulus oocyte complexes collected from each woman | immediately after oocyte retrieval |