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Effect of saffron on labor anxiety

Effect of saffron capsule on labor anxiety in primiparous women

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT201707133860N30
Enrollment
60
Registered
2017-08-08
Start date
2017-09-23
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

anxiety. Anxiety that is generalized and persistent but not restricted to, or even strongly predominating in, any particular environmental circumstances (i.e. it is

Interventions

Intervention 1: Saffron capsule In this research, Goldaro Company produced 50 g of weighed saffron powder with powdered electric pulp and percolated with 70% alcohol percolation for 72 hours extractio
Treatment - Drugs
Placebo
Saffron capsule In this research, Goldaro Company produced 50 g of weighed saffron powder with powdered electric pulp and percolated with 70% alcohol percolation for 72 hours extraction. Then, it was
Placebo Capsule In order to remove the bias in the control group, the placebo containing 250 mg of lactose powder was prepared

Sponsors

Vice Chancellor for research of Shahid Beheshti University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 35 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: age between 18 to 35, first pregnancy; single pregnancy pregnancy; embryonic cephalic presentation; gestational age 40 to 41 weeks or more based on the first day of the last menstruation and ultrasonography of the first trimester; no uterine contraction; bishop score lower or equal to 4; healthy gestational sac; regular fetal heart rate; normal non-stress test; estimated embryo weighing 2500-4000; a low risk pregnancy (no known signs of internal and surgical diseases, or complications such as preeclampsia and Placental abruption and absence of known embryonic problems); pelvic stenosis; don’t receive any herbal remedy or medication such as misoprostol, prostaglandin, Oxytocin 36 hours before treatment; no sexual intercourse from 24 hours before and up to the end of the study. Exclusion criteria: oral consumption of saffron; uterine contraction; fetal heart rate abnormalities and absence of fetal movement, use of stimulants for uterine contractions during the study; such as castor oil; midwifery requiring emergency procedures, such as intense hemorrhage.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Anxiety. Timepoint: at the time of entering the study-- when admitted to the labor sector. Method of measurement: Spielberger anxiety questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactGiti Ozgoli

Shahid Beheshti University of Medical Sciences

gozgoli@gmail.com+98 21 8820 2012

Outcome results

None listed

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