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effects of Flaxseed and Sisymbrium on cervical ripening and delivery outcome

Compare the effects of Flaxseed and Sisymbrium on cervical ripening and delivery outcome in primiparous women

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20250311065045N4
Enrollment
80
Registered
2026-01-11
Start date
2026-01-21
Completion date
Unknown
Last updated
2026-02-02

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

Conditions

Delivery.

Interventions

Intervention 1: Intervention group: 40 people in the Sisymbrium seed consumption group. For the samples in this group, 28 10-gram packets of Sisymbrium seeds will be prepared and will be provided to

Sponsors

Hamedan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: Primiparity BMI< 30 Gestational age greater than 37 weeks No acute (diarrhea, nausea, vomiting, bloating, and abdominal pain) or chronic (mental disorders, heart disease, blood pressure, diabetes) illnesses Singleton pregnancy with cephalic presentation No pregnancy complications (intrauterine growth restriction, placental abruption, placenta previa, high blood pressure, and gestational diabetes)

Exclusion criteria

Exclusion criteria: Having any contraindications for natural childbirth Use of other methods of facilitating childbirth after the start of the study Mother's unwillingness to continue cooperation Irregular use or forgetting to take the medication for more than two days The occurrence of any complications related to the consumption of flaxseed or Sisymbrium

Design outcomes

Primary

MeasureTime frame
Amount of cervical ripening. Timepoint: Time of delivery. Method of measurement: Checklist of labor information including reason for hospitalization, Bishop score upon admission, length of the first and second stages of labor, number of cases requiring induction or augmentation of pain with oxytocin, first and fifth minute Apgar, type of labor, and postpartum hemorrhage.

Secondary

MeasureTime frame
Birth outcome. Timepoint: At Delivery time. Method of measurement: Checklist of labor information including reason for hospitalization, Bishop score upon admission, length of the first and second stages of labor, number of cases requiring induction or augmentation of pain with oxytocin, first and fifth minute Apgar, type of labor, and postpartum hemorrhage.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMahsa Fadakar

Hamedan University of Medical Sciences

mahsa.fadakar94@yahoo.com+98 81 3335 2226

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 7, 2026