Lifestyle and Fertility Study (ISIS)
Recruitment status was Recruiting
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Purpose
Researchers believe that certain lifestyle factors can influence a couple's ability to conceive and have a baby. The ISIS Study will look at the health habits of couples who are planning their first pregnancy, and then attempt to measure the effect these habits have on the couple's fertility. The ISIS Study hopes to clarify the link between lifestyle and fertility, and believes that information gained in this project may help future couples in their attempts to conceive.
| Condition |
|---|
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Infertility Pregnancy Early Preconception Care Women's Health Lifestyle Factors |
| Study Type: | Observational |
| Study Design: | Observational Model: Cohort Time Perspective: Prospective |
| Official Title: | Antioxidant Status, Diet and Early Pregnancy |
- Time to pregnancy [ Time Frame: Couples will be followed from preconception to the outcome of pregnancy. ] [ Designated as safety issue: No ]Time to pregnancy is defined as the number of menstrual cycles from the cessation of contraception to a clinically recognized pregnancy.
- Early pregnancy loss [ Time Frame: First trimester of pregnancy ] [ Designated as safety issue: No ]Pregnancy and subsequent early loss will be determined by measuring urinary human chorionic gonadotropin (hCG).
Biospecimen Retention: Samples With DNA
Whole blood, plasma, serum, urine
| Estimated Enrollment: | 1150 |
| Study Start Date: | March 2008 |
| Groups/Cohorts |
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1
Healthy couples who are planning their first pregnancy.
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Detailed Description:
Only one-fourth to one-third of fertilized human eggs are likely to survive to produce a term baby. The causes of these reproductive failures are substantially unknown, but scientific evidence suggests that they may, in part, be due to exposures such as pre-conception nutrition, that may result in insults to the oocyte and periconceptual embryo. Early reproductive events may have long-lasting impact as several have recently been identified as antecedents to adult-onset diseases. The goal of this prospective epidemiologic study is to evaluate the hypothesis that increased oxidative stress results in delayed time-to-pregnancy or early pregnancy loss. Recently, reactive oxygen species (ROS) have been associated with spontaneous abortion, preeclampsia, and premature preterm rupture of the membranes in women and defective sperm function in men. In living cells ROS are formed continuously as a consequence of both biochemical reactions and external factors. In this prospective cohort study of healthy couples who are planning pregnancy, we are evaluating time-to-pregnancy, defined as the number of menstrual cycles from the cessation of contraception to a clinically recognized pregnancy, and early unrecognized pregnancy loss. Unrecognized pregnancy and subsequent early loss will be determined by measuring urinary human chorionic gonadotropin (hCG). Diet will be assessed in both partners prior to conception using the Block food frequency questionnaire and serum assays for the antioxidants vitamins C and E, the carotenoids, and selenium. Two urinary biomarkers of oxidative stress, 8-hydroxy-2'-deoxyguanosine and F2a-isoprostanes, and a serum biomarker of antioxidative capacity, oxygen radical absorbance capacity, will be measured in the women. The proposed study has a number of strengths: 1) it is large and prospective in design, with diet and oxidative stress measured prior to conception; 2) a highly sensitive and specific assay for hCG will be used to detect conceptions as early as the time of implantation; 3) dietary intake and biomarker assays of antioxidant status will be assessed twice during the preconception period using state-of-the-art assessment methods including a diet calibration substudy; 4) the proposed research has the potential to fill gaps in our understanding of the role of diet in achieving successful conception, an area where very little investigation has been done.
Eligibility| Ages Eligible for Study: | 18 Years to 39 Years |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | Yes |
| Sampling Method: | Non-Probability Sample |
We are looking for couples who are planning a pregnancy. This must be a first pregnancy for women, ages 18 to 39, and both partners must be in good general health with no history of infertility.
Inclusion Criteria:
- Female is between 18 and 39 years of age
- Female is having regular periods
- Couple is currently using some form of contraception (e.g., oral contraceptives, barrier methods, timing method), but planning to get pregnant in the near future.
Exclusion Criteria:
- Female has a previous pregnancy
- Female has tried for 12 months or more to achieve a pregnancy without success, or has undergone fertility treatment
- Female has received a diagnosis of polycystic ovary syndrome (PCOS)
- Female has another serious medical condition (e.g. heart disease, kidney disease, diabetes, thyroid disease, clinical depression, or an acute chronic infection)
- Male has tried for 12 months or more to achieve a conception without success
- Male has had a fertility related condition (e.g., zoo- or oligospermia, other abnormal semen analysis, cryptorchidism, or testicular cancer)
- Male has another serious medical condition (e.g. heart disease, kidney disease, diabetes, thyroid disease, clinical depression, or an acute chronic infection)
Contacts and Locations| Contact: Study Coordinator | 781-434-6556 | isisfertility@dartmouth.edu |
| Contact: Toll free -- contact us at: | 877-777-2581 |
| United States, Massachusetts | |
| Dartmouth Medical School/Boston IVF | Recruiting |
| Waltham, Massachusetts, United States, 02451 | |
| Contact: Study Coordinator 781-434-6556 isisfertility@dartmouth.edu | |
| Contact 877-777-2581 | |
| Principal Investigator: Marlene B. Goldman, ScD | |
| United States, New Hampshire | |
| Dartmouth-Hitchcock Medical Center | Recruiting |
| Lebanon, New Hampshire, United States, 03756 | |
| Contact: Study Coordinator 781-434-6556 isisfertility@dartmouth.edu | |
| Principal Investigator: Marlene B. Goldman, ScD | |
| United States, Pennsylvania | |
| Penn State University | Recruiting |
| University Park, Pennsylvania, United States, 16802 | |
| Contact: Terryl J. Hartman, PhD, MPH 814-865-8747 tjh9@psu.edu | |
| Principal Investigator: Terryl J. Hartman, PhD | |
| Principal Investigator: | Marlene B. Goldman, MS, ScD | Dartmouth-Hitchcock Medical Center |
More Information
Additional Information:
Publications:
| Responsible Party: | Marlene B. Goldman, ScD, Dartmouth College |
| ClinicalTrials.gov Identifier: | NCT00642590 History of Changes |
| Other Study ID Numbers: | R01 HD049762 |
| Study First Received: | March 21, 2008 |
| Last Updated: | February 13, 2011 |
| Health Authority: | United States: Federal Government |
Keywords provided by Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD):
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Fertility Pregnancy Conception Infertility |
Behavioral Lifestyle Preconception care Women's Health |
Additional relevant MeSH terms:
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Infertility Genital Diseases, Male Genital Diseases, Female |
ClinicalTrials.gov processed this record on June 17, 2013