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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00046124
Other study ID # 8957-CP-001
Secondary ID
Status Completed
Phase N/A
First received September 20, 2002
Last updated September 1, 2006

Study information

Verified date September 2006
Source National Institute of Environmental Health Sciences (NIEHS)
Contact n/a
Is FDA regulated No
Health authority United States: Federal Government
Study type Observational

Clinical Trial Summary

This prospective cohort study assesses the effects of exposure to organophosphate (OP) pesticides on adverse reproductive outcomes in both male and female agricultural workers in China. We will enroll women and their spouses, who are attempting to become pregnant, and observe reproductive endpoints including (1) semen parameters (concentration, total count, motility, progression and morphology), (2) menstrual disorders (oligomenorrhea, amenorrhea, polymenorrhea, intermenstrual bleeding, prolonged menstrual bleeding, dysmenorrhea, and irregular menstruation); (3) alterations in hormone patterns including reduced estrogen excretion (REE), anovulation, abnormal luteal phase (ALP), and abnormal follicular phase (AFP) in women and abnormalities of LH, FSH, TSH, SHBG, inhibin-B and testosterone in men; (4) fecundability; and (5) pregnancy outcomes including spontaneous abortion, preterm delivery, low birth weight, and intrauterine growth retardation.


Recruitment information / eligibility

Status Completed
Enrollment 0
Est. completion date
Est. primary completion date
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 20 Years to 34 Years
Eligibility Inclusion Criteria:

- it must be the first marriage for both the woman and her husband and they must currently live in the study area;

- the female's age must range from 20 to 34 years;

- the couple has no plan to leave the study area in which they live for the next two years.

Exclusion Criteria:

- those who are currently pregnant;

- those who have tried unsuccessfully to get pregnant for at least 1 year;

- those who are current or former smokers;

- those who plan to move in the coming year.

Study Design

Observational Model: Defined Population, Time Perspective: Longitudinal


Locations

Country Name City State
China Anhui Medical University Anqing City Anhui

Sponsors (1)

Lead Sponsor Collaborator
National Institute of Environmental Health Sciences (NIEHS)

Country where clinical trial is conducted

China, 

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