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Diet and Its Relationship With Couple Infertility

Impact of the Diet Fertility : A Case-control Multicentric Study

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01093378
Acronym
ALIFERT
Enrollment
400
Registered
2010-03-25
Start date
2009-10-01
Completion date
2015-06-01
Last updated
2026-03-04

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Infertility

Keywords

Infertility, Obesity, Dietary intake, Fertility, nutrition, diet, weight

Brief summary

This case-control multicentric study involving fertile and infertile couples aims at evaluating the impact on conception rate of nutritional parameters (biologic, clinic, anthropometric, and food questionnaire).

Detailed description

Infertility affects about 15% of couples. Many factors relating to lifestyle and environment are likely to influence fertility. As an adapted nutrition could prevent 30% of cancers, diet could be essential, but largely neglected, in the prevention of infertility. Some studies tried to explore the impact of diet on male or female fertility, but very few focused on both. The aim of our study is to assess the role of nutrition in both fertile and infertile couples, taking into account most of factors relating to lifestyle. Clinical, anthropometric (BMI, fat mass), biological markers (non specific - glycaemia, lipids, inflammation, electrolytes - and specific - vitamins E, A, C, D, B, including folates and MTHFR polymorphism) and semen analysis, will be combined with validated questionnaires (nutrition, drugs, alcohol, tobacco, physical activity, sleep and stress). The statistical analysis of correlations between nutritional and clinical data will provide information concerning the impact of nutrition on fertility.

Interventions

None listed

Sponsors

Assistance Publique - Hôpitaux de Paris
Lead SponsorOTHER
Institut National de la Santé Et de la Recherche Médicale, France
CollaboratorOTHER_GOV
University Paris 7 - Denis Diderot
CollaboratorOTHER
URC-CIC Paris Descartes Necker Cochin
CollaboratorOTHER

Study design

Observational model
CASE_CONTROL
Time perspective
CROSS_SECTIONAL

Eligibility

Sex/Gender
ALL
Age
18 Years to 45 Years
Healthy volunteers
No

Inclusion criteria

Common to both infertile and fertile couples: * Couples where both members are over eighteen and at childbearing age (≤38 for women and ≤ 45 for men) * Couples where both members agreed to take part in the study * Couples where both members completed a medical check-up and gave an informed consent. Infertile couples could be included following a medical consultation for infertility * Couples with none of its member facing any comprehension difficulty in oral or written French language * Couples where both members are affiliated to the French NHS \[national health service\] (beneficiary or legal claimant) Specific to fertile couples: \- fertile couples who naturally and spontaneously conceived a or many children with a time to conceive shorter than 12 months. Specific to infertile couples: * Infertile couples (primary, infertility, inability to conceive a child after 12 months of unprotected sexual intercourse) * Couples where the male partner has sperm parameters compatible with a natural conception * Couples where the female partner does not present anovulation, ovarian insufficiency and or any uterus-tubal pathology

Exclusion criteria

Common to both infertile and fertile couples: * couples where one of the members is under eighteen or not a childbearing age (\>38 for women an \>45 for men) * couples where at least one member refused to give written agreement for the study * couples where at least one member shows any known cardiovascular risk (diabetes, hypercholesterolemia, HBR) * couples where at least one member shows any known cardiovascular pathology, digestive pathology, no good absorptive pathology or a cancer * couples where at least one member faces some difficulty in understanding French language * couples where at least one member is not affiliated with the French NHS (beneficiary or legal claimant) Specific to fertile couples: •Couples where the woman had a miscarriage or medical termination of pregnancy with current partner Specific to infertile couples: * Couples in which it is not the first pregnancy * Couples with the male member showing either: * severe oligozoospermia (\<5 millions/ml) or a confirmed azoospermia (absence of spermatozoid in the ejaculate) * a moderate non idiopathic oligozoospermia (5-20 millions/ml), related to one more of the following factors: 1. toxic (chemotherapy, radiotherapy, drugs with a demonstrated effect on spermatogenesis) 2. infectious 3. anatomic: vasectomy, congenital anomaly (agenesis of vas deferens), long post-traumatic ischemia 4. endocrine: hypogonadotropic, hypogonadism 5. cytogenetic: klinefelter syndrome, translocation * couples whose male partner shows an abnormality of the male genital tractus : VARICOCEME undescended,testis, testicular volume \< 12ml * couples whose female partner presents an anovulation, ovarian insufficiency or a proven uterus-tubal pathology

Design outcomes

Primary

MeasureTime frame
Evaluate the nutritional status of fertile and infertile couples (food questionnaire - biologic, anthropometric and clinical balance).24 hours

Secondary

MeasureTime frame
Impact of genetic polymorphism on clinical and biological phenotypes linked to food behaviour in infertility context (MTHFR polymorphism for folates metabolism)12 months
Impact of lifestyle (alcohol and tabacco consumption, physical activity, anxiety and sleep) on diet and fertility24 hours
Impact of nutritional status on fertility and ART parameters24 hours
Fertility : time to pregnancy (TTP)in the 6 months
Male infertility : quantitative or qualitative semen abnormalitiesin the 6 months
Pregnancy and obstetrical pathologies, prematurity, twin birth, weight of the new-born in infertile couplesin the 6 months
ART parameters, if appropriatein the 6 months

Countries

France

Contacts

PRINCIPAL_INVESTIGATORRachel Levy, MD, PhD

Assistance Publique - Hôpitaux de Paris

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 18, 2026