Skip to content

Saffron in the treatment of postmenopausal hot flash

Saffron in the treatment of postmenopausal hot flash : a double-blind,randomised and placebo-controlled trial

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT201602031556N85
Enrollment
50
Registered
2016-02-04
Start date
2016-02-20
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

Hot flashing. Menopausal and female climacteric states

Interventions

Intervention 1: Capsule Saffron 30mg/day as intervention group for 6 weeks. Intervention 2: Capsule placebo as intervention group for 6 weeks.
Treatment - Drugs
Placebo
Capsule Saffron 30mg/day as intervention group for 6 weeks
Capsule placebo as intervention group for 6 weeks

Sponsors

Tehran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
45 Years to 65 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: women aged between 45-65 years old; menopause. Exclusion criteria: moderate to severe post-menopausal hot flushing-five episodes per day from 2 months ago; sopping of the mens from 12 month ago; receiving estrogen or progesterone during the last two months; receiving antidepressants during the last month; receving Selective Estrogen Receptor Modulators including raloxifen and tamoxifen during the last month; receiving aromatase inhibitors such as Anastrozole, Letrozole, Exemestane during the last month;receving Leuprolide acetate during the last month; receiving clonidine during the last month; receving gabapentine and pregabalin during the last month; receiving hot flushing reducing medications during the last month; receiving amino acid supplements during the last month.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Severity of hot flashing. Timepoint: Baseline and 2, 4, 6 weeks after beginnig of treatment. Method of measurement: By Hot flash Related Daily Interference.

Secondary

MeasureTime frame
Severity of depression. Timepoint: Baseline and 2, 4, 6 weeks after beginnig of treatment. Method of measurement: By Hamilton Depression Rating scale.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactProf. Shahin Akhondzadeh

Tehran University of Medical Sciences

S.akhond@sina.tums.ac.ir+98 21 5541 2222

Outcome results

None listed

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