NCT Number: NCT00618865
Omega-3 Fatty Acids for Major Depressive Disorder During Pregnancy
Whether high-dose omega-3 fatty acids supplement would be an effective treatment in patients with major depressive disorder during pregnancy and breast-feeding.
Looking for future studies?
Notify MeKey information
Age range
18 year–40 year
Sex eligibility
Female
Study type
Interventional
Phase
Not applicable
Who can participate
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
- Eligible participants were pregnant women, aged 18 to 40 years, with major depressive disorder onset between their 16th week (second trimester) and 32nd week (third trimester) of gestation at the Department of Obstetrics.
Exclusion criteria
- Subjects were excluded with a DSM-IV diagnosis of bipolar disorders, psychotic disorders, substance abuse or dependence for at least 3 months, or any Axis-II diagnosis of borderline or antisocial personality disorder.
Treatment and study plan
Sponsors and collaborators
Lead sponsor
National Science and Technology Council, Taiwan
Other Gov
Registry information
Official study title
Omega-3 Polyunsaturated Fatty Acids in Women With Major Depressive Disorders During Pregnancy
Important dates
- Study start
- 2004
- Primary completion
- 2004
- Study completion
- 2004
- First posted
- Feb 20, 2008
- Registry last updated
- Feb 20, 2008
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
Related clinical trials
Published trials that share one or more normalized conditions with this study.
Trial of Transcranial Photobiomodulation for Depression With PET and EEG Outcomes
NCT06934135
Anxiety Disorders, Behavior
Lima, Peru
View Trial DetailsOptimizing tDCS Protocol for Clinical Use in Major Depressive Disorder
NCT06165445
Cognition Disorders, Cognitive Dysfunction
Zanjan, Zanjan Province, Iran
View Trial DetailsPharmacogenomic-Guided Antidepressant Drug Prescribing in Cancer Patients
NCT03674138
Anxiety, Anxiety Disorders
Tampa, Florida, United States
View Trial DetailsEffect of Probiotic Supplement on Improvement of Depressive Symptoms in Patients With Substance-Induced Depressive Disorder
NCT06790823
Depressive Disorder, Depressive Disorder, Major
Shiraz, Fars, Iran
View Trial Details