IVFNCT05865015
Nutritional Status of Women Undergoing in Vitro Fertilization
An observational study of IVF and Body Weight, run by University Medical Centre Ljubljana at 2 sites in Slovenia.
Trial summary
Infertility affects around 15 % of couples in their reproductive years. Even though the use of assisted reproductive technologies (ART) in aforementioned couples is increasing, their success rate is still relatively low. Read more about this study
- Who is it for?
- Ages 20 to 39 years, women onlyHealthy volunteers can take part
- Conditions the study is for
- IVF, Body Weight, Nutrient Deficiency
- How many people
- 69 participants
- Where
- 2 sitesSlovenia
- Study dates
- 5 Jan 2023to 10 Sep 2023
- Phase
- Observational
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 20 to 39 years
- Women only
- Healthy volunteers accepted
- Adult
Study population: Women undergoing IVF treatment at the University Medical Centre Ljubljana.
Who may be able to join
- Undergoing IVF/ICSI treatment
Who cannot join
- Women's age > 39
- Endometriosis
Trial locations and contacts
2 sites in 1 country.
Slovenia2 sites
Division of Ob/Gyn, University Medical Centre Ljubljana
Ljubljana, 1000
Division of Peadiatrics, University Medical Centre Ljubljana
Ljubljana, 1000
About this study
Official title: Dietary Patterns, Physical Activity Level, Body Composition and Serum Vitamin B9, Vitamin B12 and Vitamin D Levels in Women Undergoing in Vitro Fertilization and the Outcomes of in Vitro Fertilization
Infertility affects around 15 % of couples in their reproductive years. Even though the use of assisted reproductive technologies (ART) in aforementioned couples is increasing, their success rate is still relatively low. Hence it is important to identify and better understand potential modifiable dietary and lifestyle risk factors that may influence the success of ART. This study will include women undergoing IVF with a view to investigating the relationship between preconception dietary patterns, body composition, physical activity level, serum values of vitamin B9, vitamin B12 and vitamin D and the outcomes of IVF, such as the number of obtained oocytes, fertilization rate and clinical pregnancy. Main hypothesis is that women undergoing IVF, who eat a balanced diet, maintain healthy body weight and have adequate serum levels of vitamin B9, vitamin B12 and vitamin D, have a higher chance of achieving better IVF outcomes.
Read the detailed description
Infertility, which affects around 15 % of couples of reproductive, refers to the inability of a couple to conceive after 12 months of unprotected sex. Pre-conception dietary habits have been shown to influence the outcomes of the in vitro fertilization (IVF) procedure, such as oocyte and embryo quality, embryo implantation and successful pregnancy. Thus far, a balanced diet, especially a Mediterranean diet (MED), is known to have a beneficial effect on the outcome of IVF in women before the IVF process. MED is characterised by a high intake of antioxidants that reduces oxidative stress, which otherwise increases the likelihood of infertility in women. In addition, the Mediterranean diet is characterised by a higher intake of folate and polyunsaturated omega-3 fatty acids (especially eicosapentaenoic acid), which also has a beneficial effect on the outcome of the IVF process. While some authors have not confirmed that the Mediterranean diet can increase the likelihood of pregnancy after IVF in infertile women, they have found that it can increase the number of embryos ready for transfer. On the other hand, an unbalanced diet with a typically low intake of vitamins and minerals has an adverse effect on fertility. Low intakes of vitamins B6, B9 and B12 are particularly problematic, as their deficiency leads to the accumulation of homocysteine, which can lead to hyperhomocysteinemia. Elevated levels of homocysteine in follicular fluid are known to negatively affect the number of retrieved oocytes and embryo quality in IVF and intracytoplasmic sperm injection (ICSI). Higher serum levels of vitamin B9 and vitamin B12 in women have been shown to increase the likelihood of a live birth after ART, as they have a beneficial effect on pregnancy maintenance after embryo implantation. Despite the known importance of sufficient vitamin B9 and vitamin B12 intake to support fertility and success of the IVF procedure, some women undergoing IVF still have largely insufficient serum levels of vitamin B9 and vitamin B12 prior to the IVF procedure. Vitamin D deficiency in women has also been identified as a modifiable risk factor that may affect the outcome of ART. Vitamin D is involved in steroid formation in the ovary and in the expression of genes in the endometrium that are crucial for embryo implantation. For this reason, women should have their serum vitamin D levels routinely checked before IVF. This would allow women with an identified vitamin D deficiency to start vitamin D supplementation, which may have a beneficial effect on IVF outcome. Another modifiable factor with an impact on ART outcome is excessive body weight and obesity, as adipose tissue interferes with the synthesis and bioavailability of sex hormones in women, which negatively affects oocyte quality and endometrial receptivity. In this group of women, oocytes are less likely to properly develop after IVF than oocytes from women with optimal body weight. In addition, it is known that women who are overweight or obese have a lower probability of embryo implantation, clinical pregnancy and live birth after IVF/ICSI. However, in women with obesity, regular physical activity can have a positive effect on IVF/ICSI outcomes even when body mass index is unchanged. Consequently, the time before the ART procedure presents an opportunity to establish nutritional counselling to facilitate women's achievement of optimal body weight and intake of the necessary micronutrients, which could positively influence the outcome of the ART procedure. However further studies on the impact of women's dietary habits and nutritional status on the outcome of the ART procedure are urgently needed before this can be done.
The investigators aim to identify which modifiable risk factors for IVF/ICSI failure are poorly managed in women and to improve understanding of the impact of women's dietary habits, physical. The investigators are interested in whether women have a balanced diet before the IVF/ICSI procedure and whether they successfully prevent vitamin B9, vitamin B12 and vitamin D deficiencies, which can negatively affects the outcomes of IVF/ICSI. By measuring women's body composition before IVF/ICSI, the investigators aim to test whether an excessive percentage of fat mass reduces the likelihood of IVF/ICSI success, as suggested by the scientific evidence to date. The information obtained will allow the design of future nutritional counselling for women before IVF/ICSI to facilitate the establishment of a healthier lifestyle and potentially increase the likelihood of success of the IVF/ICSI procedure, thereby reducing the economic burden of infertility treatment. In the first study of its kind in Slovenia, the investigators expect to identify the association between dietary habits, physical activity levels, body composition and serum levels of vitamin B9, vitamin B12 and vitamin D and IVF/ICSI outcomes, such as the number of retrieved oocytes, the rate of fertilisation of oocytes and clinical pregnancy, in women prior to undergoing IVF/ICSI. The underlying hypothesis is that women who have a balanced diet and lead a healthier lifestyle prior to IVF/ICSI will have a higher likelihood of favourable IVF/ICSI outcomes.
The research will be conducted at the Clinical Department of Reproduction, Department of Gynaecology, University Clinical Centre Ljubljana, with the collaboration of the Faculty of Biotechnology, University of Ljubljana. The study will be cross-sectional, non-interventional. Patients will be introduced to the study and its process at the time of entering the IVF/ICSI procedure. If the patient signs the informed consent form, the investigators will obtain her height and weight measurement and body composition measurement by non-invasive bioimpedance analysis. The patient will also fill in the questionnaire required for the study, which includes questions regarding sociodemographic status, dietary habits, frequency of food consumption in the past month, and physical activity level. In addition, prior to the IVF/ICSI procedure, the patient will have blood drawn for biochemical laboratory tests at the Clinical Institute of Clinical Chemistry and Biochemistry, University Clinical Centre Ljubljana (in addition to the standard tests, the investigators will also determine vitamin B9 or folate and folic acid, vitamin B12, vitamin D, oligoelements, heavy metals, hormone disruptors, etc.) The protection of personal data will be guaranteed, as each blood sample will be labelled or recorded during the study under a code identical to the code of the questionnaire completed by the patient. Information on the results of the IVF/ICSI procedure will be obtained from the patients' medical records with their consent. Statistical evaluation of the data will be performed at the Faculty of Biotechnology, University of Ljubljana. The data obtained will be subjected to appropriate statistical analysis to determine the association of dietary habits, body composition, physical activity level and serum vitamin B9, vitamin B12 and vitamin D levels of patients before the IVF/ICS procedure on IVF/ICS outcomes.
- Conditions
- IVF, Body Weight, Nutrient Deficiency, Dietary Vitamin B12 Deficiency Anemia, Dietary Folate Deficiency Anemia
- Keywords
- Dietary Patterns, Mediterranean diet, In Vitro Fertilization, Diet, Fertility, Infertility, Assisted Reproduction
- Medical subject headings
- Body Weight, Infertility
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Other
What is being measured
The primary outcome is the main question the study is designed to answer.
Oocyte number
Total Number of oocytes produced.
Measured: 3 months
Secondary outcomes (1)
Fertilization rate
Fertilization rate will be determined on day 1 after the IVF/intracytoplasmatic sperm injection procedure, and is going to calculated as the number of fertilized oocytes divided by the total number of oocytes retrieved.
Measured: 3 months
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted18 May 2023
- Study start5 Jan 2023
- Primary completion2 Mar 2023
- Study completion10 Sep 2023
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for IVFStudies of the same condition, open and under way.
- More trials run by University Medical Centre LjubljanaThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Observational
- Observational model
- Cohort
- Time perspective
- Cross-sectional
- Enrolment
- 69 participants (actual)
Sponsor and investigators
- Lead sponsor
- University Medical Centre Ljubljana
- Sponsor type
- University, hospital or other
- Responsible party
- Sponsor
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT05865015
- Sponsor's protocol ID
- TP20210218
- Status last verified
- Feb 2024
- First submitted
- 9 May 2023
- Last updated
- 9 May 2024
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- Undecided
Study at a glance
From the registry record, last updated by the sponsor on 9 May 2024. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Dietary Patterns, Physical Activity Level, Body Composition and Serum Vitamin B9, Vitamin B12 and Vitamin D Levels in Women Undergoing in Vitro Fertilization and the Outcomes of in Vitro Fertilization
- ClinicalTrials.gov ID
- NCT05865015
- Acronym / sponsor ID
- TP20210218
- Conditions
- IVF, Body Weight, Nutrient Deficiency, Dietary Vitamin B12 Deficiency Anemia, Dietary Folate Deficiency Anemia
- Keywords
- Dietary Patterns, Mediterranean diet, In Vitro Fertilization, Diet, Fertility, Infertility, Assisted Reproduction
- Study type
- Observational
- Recruitment status
- Completed
- Enrolment
- 69 participants (actual)
- Lead sponsor
- University Medical Centre LjubljanaUniversity, hospital or other
- Study start
- 5 Jan 2023 (actual)
- Primary completion
- 2 Mar 2023 (actual)
- Study completion
- 10 Sep 2023 (actual)
- First posted
- 18 May 2023 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
Infertility affects around 15 % of couples in their reproductive years. Even though the use of assisted reproductive technologies (ART) in aforementioned couples is increasing, their success rate is still relatively low. Hence it is important to identify and better understand potential modifiable dietary and lifestyle risk factors that may influence the success of ART. This study will include women undergoing IVF with a view to investigating the relationship between preconception dietary patterns, body composition, physical activity level, serum values of vitamin B9, vitamin B12 and vitamin D and the outcomes of IVF, such as the number of obtained oocytes, fertilization rate and clinical pregnancy. Main hypothesis is that women undergoing IVF, who eat a balanced diet, maintain healthy body weight and have adequate serum levels of vitamin B9, vitamin B12 and vitamin D, have a higher chance of achieving better IVF outcomes.
Detailed description
Infertility, which affects around 15 % of couples of reproductive, refers to the inability of a couple to conceive after 12 months of unprotected sex. Pre-conception dietary habits have been shown to influence the outcomes of the in vitro fertilization (IVF) procedure, such as oocyte and embryo quality, embryo implantation and successful pregnancy. Thus far, a balanced diet, especially a Mediterranean diet (MED), is known to have a beneficial effect on the outcome of IVF in women before the IVF process. MED is characterised by a high intake of antioxidants that reduces oxidative stress, which otherwise increases the likelihood of infertility in women. In addition, the Mediterranean diet is characterised by a higher intake of folate and polyunsaturated omega-3 fatty acids (especially eicosapentaenoic acid), which also has a beneficial effect on the outcome of the IVF process. While some authors have not confirmed that the Mediterranean diet can increase the likelihood of pregnancy after IVF in infertile women, they have found that it can increase the number of embryos ready for transfer. On the other hand, an unbalanced diet with a typically low intake of vitamins and minerals has an adverse effect on fertility. Low intakes of vitamins B6, B9 and B12 are particularly problematic, as their deficiency leads to the accumulation of homocysteine, which can lead to hyperhomocysteinemia. Elevated levels of homocysteine in follicular fluid are known to negatively affect the number of retrieved oocytes and embryo quality in IVF and intracytoplasmic sperm injection (ICSI). Higher serum levels of vitamin B9 and vitamin B12 in women have been shown to increase the likelihood of a live birth after ART, as they have a beneficial effect on pregnancy maintenance after embryo implantation. Despite the known importance of sufficient vitamin B9 and vitamin B12 intake to support fertility and success of the IVF procedure, some women undergoing IVF still have largely insufficient serum levels of vitamin B9 and vitamin B12 prior to the IVF procedure. Vitamin D deficiency in women has also been identified as a modifiable risk factor that may affect the outcome of ART. Vitamin D is involved in steroid formation in the ovary and in the expression of genes in the endometrium that are crucial for embryo implantation. For this reason, women should have their serum vitamin D levels routinely checked before IVF. This would allow women with an identified vitamin D deficiency to start vitamin D supplementation, which may have a beneficial effect on IVF outcome. Another modifiable factor with an impact on ART outcome is excessive body weight and obesity, as adipose tissue interferes with the synthesis and bioavailability of sex hormones in women, which negatively affects oocyte quality and endometrial receptivity. In this group of women, oocytes are less likely to properly develop after IVF than oocytes from women with optimal body weight. In addition, it is known that women who are overweight or obese have a lower probability of embryo implantation, clinical pregnancy and live birth after IVF/ICSI. However, in women with obesity, regular physical activity can have a positive effect on IVF/ICSI outcomes even when body mass index is unchanged. Consequently, the time before the ART procedure presents an opportunity to establish nutritional counselling to facilitate women's achievement of optimal body weight and intake of the necessary micronutrients, which could positively influence the outcome of the ART procedure. However further studies on the impact of women's dietary habits and nutritional status on the outcome of the ART procedure are urgently needed before this can be done.
The investigators aim to identify which modifiable risk factors for IVF/ICSI failure are poorly managed in women and to improve understanding of the impact of women's dietary habits, physical. The investigators are interested in whether women have a balanced diet before the IVF/ICSI procedure and whether they successfully prevent vitamin B9, vitamin B12 and vitamin D deficiencies, which can negatively affects the outcomes of IVF/ICSI. By measuring women's body composition before IVF/ICSI, the investigators aim to test whether an excessive percentage of fat mass reduces the likelihood of IVF/ICSI success, as suggested by the scientific evidence to date. The information obtained will allow the design of future nutritional counselling for women before IVF/ICSI to facilitate the establishment of a healthier lifestyle and potentially increase the likelihood of success of the IVF/ICSI procedure, thereby reducing the economic burden of infertility treatment. In the first study of its kind in Slovenia, the investigators expect to identify the association between dietary habits, physical activity levels, body composition and serum levels of vitamin B9, vitamin B12 and vitamin D and IVF/ICSI outcomes, such as the number of retrieved oocytes, the rate of fertilisation of oocytes and clinical pregnancy, in women prior to undergoing IVF/ICSI. The underlying hypothesis is that women who have a balanced diet and lead a healthier lifestyle prior to IVF/ICSI will have a higher likelihood of favourable IVF/ICSI outcomes.
The research will be conducted at the Clinical Department of Reproduction, Department of Gynaecology, University Clinical Centre Ljubljana, with the collaboration of the Faculty of Biotechnology, University of Ljubljana. The study will be cross-sectional, non-interventional. Patients will be introduced to the study and its process at the time of entering the IVF/ICSI procedure. If the patient signs the informed consent form, the investigators will obtain her height and weight measurement and body composition measurement by non-invasive bioimpedance analysis. The patient will also fill in the questionnaire required for the study, which includes questions regarding sociodemographic status, dietary habits, frequency of food consumption in the past month, and physical activity level. In addition, prior to the IVF/ICSI procedure, the patient will have blood drawn for biochemical laboratory tests at the Clinical Institute of Clinical Chemistry and Biochemistry, University Clinical Centre Ljubljana (in addition to the standard tests, the investigators will also determine vitamin B9 or folate and folic acid, vitamin B12, vitamin D, oligoelements, heavy metals, hormone disruptors, etc.) The protection of personal data will be guaranteed, as each blood sample will be labelled or recorded during the study under a code identical to the code of the questionnaire completed by the patient. Information on the results of the IVF/ICSI procedure will be obtained from the patients' medical records with their consent. Statistical evaluation of the data will be performed at the Faculty of Biotechnology, University of Ljubljana. The data obtained will be subjected to appropriate statistical analysis to determine the association of dietary habits, body composition, physical activity level and serum vitamin B9, vitamin B12 and vitamin D levels of patients before the IVF/ICS procedure on IVF/ICS outcomes.
Study design
- Observational model
- Cohort
- Time perspective
- Cross-sectional
Who may qualify
- Ages
- 20 to 39 years
- Sex
- Female only
- Healthy volunteers
- Accepted
- Age groups
- Adult
- Study population
- Women undergoing IVF treatment at the University Medical Centre Ljubljana.
Key inclusion criteria (1 listed)
- Undergoing IVF/ICSI treatment
Key exclusion criteria (2 listed)
- Women's age > 39
- Endometriosis
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Other | – |
Primary outcome
Oocyte number
Time frame: 3 months
Total Number of oocytes produced.
1 secondary outcome
Fertilization rate
Time frame: 3 months
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 9 May 2024.
- Individual participant dataSharing planned: Undecided
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
The record lists no contact. Use the official record to reach the sponsor.
2 sites in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
An observational study of IVF and Body Weight, run by University Medical Centre Ljubljana at 2 sites in Slovenia.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 1 inclusion and 2 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: finished, as of the sponsor's last update on 9 May 2024. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 2 sites in Slovenia. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Oocyte number (time frame: 3 months). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 9 May 2024.