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Can your diet boost your chances of getting pregnant?

NCT ID NCT01093378

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed This study
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 27, 2026 · Last updated Jun 27, 2026

Summary

This study looked at 400 couples to understand how diet, lifestyle habits like smoking and exercise, and genetics influence fertility. Researchers compared fertile and infertile couples to find nutritional factors that may help or hinder conception. No treatment was given; the goal was to gather information for future guidance.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Participants

400 people

The number who actually took part.

Start date

Oct 2009

Finished

Jun 2015

Lead sponsor

Other sponsor

The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Who is studied

Defined population after a screening in out-hospitalized patients in selected investigation sites

Ages

18 to 45 years

Sex

Anyone

Healthy volunteers

Not accepted

This study is not open to healthy volunteers. The entry requirements below say who it is open to.

Show the full entry requirements

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

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

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Conditions

The condition(s) this trial relates to.

Body Weight infertility disorder Obesity

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Contacts and locations

Locations

  • Laboratoire d'Histologie- Embryologie - Cytogénétique - CECOS

    Bondy, 93143, France

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Other studies related to the condition(s) this trial covers.