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Effect of Prednisolone and Promethazine in Hyperemesis Gravidarum: A Double Blind Clinical Trial Study

Effect of Prednisolone and Promethazine in Hyperemesis Gravidarum: A Double Blind Clinical Trial Study

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT201104231760N12
Enrollment
70
Registered
2011-05-30
Start date
2006-10-17
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

Hyperemesis gravidarum. Excessive vomiting in pregnancy

Interventions

Intervention 1: group I (control): Prednisone 5 mg as capsule, three times daily for a week. In the second week in both treatment groups every three days decreased capsule gradually treatment was stop
Treatment - Drugs
group I (control): Prednisone 5 mg as capsule, three times daily for a week. In the second week in both treatment groups every three days decreased capsule gradually treatment was stopped in the secon
group II (case): Promethazine 25 mg as capsule three times daily for a week. In the second week in both treatment groups every three days decreased capsule gradually treatment was stopped in the secon

Sponsors

Vice Chancellor for Research and Technology
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 35 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: Women 18 to 35 years, First or second pregnancy, Less than 16 weeks gestational age according to last menstrual period and ultrasound, Vomiting more than three times a day with no response to outpatient treatment, Weight loss over 3 kg and a positive urine ketone. Exclusion criteria: Concurrent Medical diseases, Anti-emetic drugs with in three days, Hydatid form mole, Twin pregnancy and iron supplementation.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Severity of nausea and vomiting. Timepoint: The first day, second, third, fourth, 14th (end of treatment) and 28th (two weeks after treatment). Method of measurement: Visual Analoge Scale and the number of vomiting per day.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactNargess Gholizadeh Pasha

Fatemehzahra Fertility & reproductive Health Research Center

ngh_pa@yahoo.com+98 11 1227 4881

Outcome results

None listed

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