Use of Juice+ food supplements, when initiated in the first trimester and used continuously thereafter, will result in a lower incidence of preeclampsia and pregnancy complications. Study sponsored by National Safety Associates, LLC.
Official Title
Minimising Early Pregnancy Oxidative Stress to Maximise Healthy Pregnancy Outcome: Reducing Preeclampsia and Reproductive Loss With Antioxidant-Rich Tablet Supplementation Initiated in the First Trimester
Conditions
- Preeclampsia
- Pregnancy Loss
Study Type
Observational
Study Design
Case Control, Prospective
Further Details
-
Development of preeclampsia during pregnancy
Secondary Outcome Measures:
-
The observed incidence of preterm labor, premature rupture of membranes, perinatal loss
Biospecimen Retention: Samples Without DNA
Study Start
May 2004
Eligibility & Criteria
Official Title
Minimising Early Pregnancy Oxidative Stress to Maximise Healthy Pregnancy Outcome: Reducing Preeclampsia and Reproductive Loss With Antioxidant-Rich Tablet Supplementation Initiated in the First Trimester
Conditions
- Preeclampsia
- Pregnancy Loss
Study Type
Observational
Study Design
Case Control, Prospective
Further Details
-
Development of preeclampsia during pregnancy
Secondary Outcome Measures:
-
The observed incidence of preterm labor, premature rupture of membranes, perinatal loss
Biospecimen Retention: Samples Without DNA
Study Start
May 2004
Eligibility & Criteria
Eligibility
- Ages Eligible for Study: 18 Years to 44 Years
- Genders Eligible for Study: Female
- Accepts Healthy Volunteers: No
- Sampling Method: Non-Probability Sample
Study Population
Patients cared for in the University of Mississippi Medical Center
Inclusion Criteria:
- Pregnant Patients seen in first trimester with low or high risk pregnancy
Exclusion Criteria:
- Pregnant patients first seen after the first trimester
- Unlikely to continue care in our system
- Unwilling to comply with rigor of taking food supplements throughout gestation
Total Enrolment
600
Contact Details
Please refer to this study by its ClinicalTrials.gov identifier: NCT00583635
Contacts
Contact: James N Martin, Jr, MD 601-984-6719 jnmartin@ob-gyn.umsmed.edu
Locations
United States, Mississippi
University of Mississippi Medical Center Recruiting
Jackson, Mississippi, United States, 39216
Contact: James N Martin, Jr., MD 601-984-6719 jnmartin@ob-gyn.umsmed.edu
Contact: Pamela Tazik 601-815-5007 ptazik@dor.umsmed.edu
Principal Investigator: James N Martin, Jr, MD
Sponsors and Collaborators
University of Mississippi Medical Center
Investigators
Principal Investigator: James N Martin, Jr., MD University of Mississippi Medical Center
Total Enrolment
600
Contact Details
Please refer to this study by its ClinicalTrials.gov identifier: NCT00583635
Contacts
Contact: James N Martin, Jr, MD 601-984-6719 jnmartin@ob-gyn.umsmed.edu
Locations
United States, Mississippi
University of Mississippi Medical Center Recruiting
Jackson, Mississippi, United States, 39216
Contact: James N Martin, Jr., MD 601-984-6719 jnmartin@ob-gyn.umsmed.edu
Contact: Pamela Tazik 601-815-5007 ptazik@dor.umsmed.edu
Principal Investigator: James N Martin, Jr, MD
Sponsors and Collaborators
University of Mississippi Medical Center
Investigators
Principal Investigator: James N Martin, Jr., MD University of Mississippi Medical Center
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