Survey and comparison of the efficacy of Granisetron and Promethazine in control of Hyperemesis Gravidarum
Not Applicable
- Conditions
- Hyperemesis gravidarum.Hyperemesis gravidarum with metabolic disturbance
- Registration Number
- IRCT201108144927N2
- Lead Sponsor
- Aburaihan Pharmaceutical Company
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- Female
- Target Recruitment
- 120
Inclusion Criteria
the women in the 20 weeks of pregnancy; referred to gynecology and obstetrics emergency room in Dr.Shariati hospital; inappropriate response to outpatient antiemetic therapies; presenting more than one plus ketonuria in complete analysis of urine; nausea and vomiting score more than 13 (according to the pregnancy unique qualification of emesis) and signing the study written consent.
Exclusion criteria: molar pregnancy and sever thyroid or liver disease
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method ausea. Timepoint: 48 hours. Method of measurement: Physical examination.;Vomoting. Timepoint: 48 hours. Method of measurement: Physical examination.
- Secondary Outcome Measures
Name Time Method