Efficacy evaluation of concurrent Zingiber and Vitamin B6 in morning sickness of pregnant wome
Phase 1
Recruiting
- Conditions
- morning sickness.Vomiting of pregnancy, unspecified
- Registration Number
- IRCT2017080635529N1
- Lead Sponsor
- Deputy of Resaerch, TUMS
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- Female
- Target Recruitment
- 240
Inclusion Criteria
Inclusion Criteria: Pregnant women with nausea or vomiting in the first 17 weeks of pregnancy; no other underlying conditions; no other medications; no history of hospitalization due to severe nausea and vomiting; no hyperemesis gravidarum; no history of hypersensitivity to ginger or vitamin B6; non pregnancy of twin or multiplexes.
Exclsion criteria: Serious complications following the use of ginger and vitamin B6; Very severe nausea (hyperemesis gravidarum) during the study, which leads to hospitalization; other drugs used to control nausea.
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Severity of nausea. Timepoint: 2 time daily for 4 days. Method of measurement: Qualitative.
- Secondary Outcome Measures
Name Time Method Reduce of vomiting severity by medication. Timepoint: 2 times daily for 4 days. Method of measurement: Qualitative.