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The effect of Saccharomyces Cerevisiae enriched with selenium and mineral selenium on postpartum depression and sexual satisfaction

Comparison of the effect of Saccharomyces Cerevisiae enriched with selenium and mineral selenium on postpartum depression and sexual satisfaction:A triple-blind randomized controlled trial

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20110606006709N23
Enrollment
108
Registered
2021-09-13
Start date
2021-08-02
Completion date
Unknown
Last updated
2021-11-01

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Postpartum Depression. Postpartum mood disturbance

Interventions

Intervention 1: Intervention group 1: Capsules containing Saccharomyces Cerevisiae enriched with selenium 200 micrograms, one for 8 weeks. Drugs will be made in the Faculty of Nutrition of Tabriz Uni

Sponsors

Tabriz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 45 Years

Inclusion criteria

Inclusion criteria: Women over 18 years who are in the first 15 to 90 days after giving birth. Willingness to participate in research Having a record of care in health centers

Exclusion criteria

Exclusion criteria: A score above 23 on the Edinburgh Questionnaire History of depression or any other mental disorder Death or hospitalization of the baby in the intensive care unit Stillbirth Hospitalization of the mother due to postpartum complications Having chronic diseases such as liver and kidney disease Allergy to fungi and yeast Loss of loved ones between two months before delivery and two months after delivery Having frequent miscarriages and having a history of infertility Having a history of a child with a mental or physical disability Divorce over the past three months

Design outcomes

Primary

MeasureTime frame
Depression score. Timepoint: Before and after the intervention at intervals of 8 weeks. Method of measurement: Edinburgh Depression Inventory.;Sexual satisfaction. Timepoint: Before and after the intervention at intervals of 8 weeks. Method of measurement: Sexual Satisfaction Questionnaire.

Secondary

MeasureTime frame
Side events. Timepoint: During 8 weeks of intervention. Method of measurement: Side accident assessment form.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactParnian Rahimi

Tabriz University of Medical Sciences

parnian9797.md@gmail.com+98 41 3475 3906

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026