Skip to content

Ginger and Ondansetron tablets on Nausea and Vomiting in pregnancy

Comparison The effect of Ondansetron versus Ginger on Nausea and Vomiting in pregnancy

Status
Recruiting
Phases
Phase 2
Study type
Interventional
Source
IRCT
Registry ID
IRCT20171007036600N1
Enrollment
116
Registered
2018-02-18
Start date
2018-02-20
Completion date
Unknown
Last updated
2018-03-26

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

Conditions

Nausea and Vomiting in pregnancy. Vomiting of pregnancy, unspecified

Interventions

Intervention 1: Control group: administration of Ginger tablet, 500 mg, every 8 hours for three days. Intervention 2: Intervention group: administration of Ondanstron tablet, 4 mg, every 8 hours for t

Sponsors

Ahvaz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 35 Years

Inclusion criteria

Inclusion criteria: Age between 18-35 years Gestational age 10-15 weeks Single pregnancy knowing the exact time of last menstrual period (LMP) or having a precised sonographic result Ability to read and write

Exclusion criteria

Exclusion criteria: The presence of diseases such as kidney disease, high blood pressure, epilepsy, diabetes and hepatitis, digestive diseases that may lead to nausea and vomiting Unwanted pregnancy Severe vomiting in pregnancy Smoking Symptoms of abortion; miscarriage or molar pregnancy Pregnancy following infertility Undesirable events in the past, such as severe disagreement with a partner, death of spouse or first degree relatives Consuming agents such as iron that exacerbate nausea and vomiting during the last week Consuming anti-inflammatory drugs for at least 3 days Sensitivity to ginger

Design outcomes

Primary

MeasureTime frame
Severity of Nausea. Timepoint: Before intervention and three days after that. Method of measurement: Rodes standard questionnaire.;Rate of Nausea. Timepoint: Before intervention and three days after that. Method of measurement: Rodes standard questionnaire.;Duration of Nausea. Timepoint: Before intervention and three days after that. Method of measurement: Rodes standard questionnaire.;Severe Vomiting. Timepoint: Before intervention and three days after that. Method of measurement: Rodes standard questionnaire.;Rate of Vomiting. Timepoint: Before intervention and three days after that. Method of measurement: Rodes standard questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMitra Tadayon Najafabady

Ahvaz University of Medical Sciences

mitratadayon2000@yahoo.com+98 61 3373 8331

Outcome results

None listed

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