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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT00405626
Other study ID # Hompostpartum-HMO-CTIL
Secondary ID
Status Not yet recruiting
Phase Phase 1
First received November 29, 2006
Last updated November 29, 2006
Start date April 2007
Est. completion date September 2007

Study information

Verified date February 2006
Source Hadassah Medical Organization
Contact David Mankuta, MD
Phone 5791070
Email mankuta@yahoo.com
Is FDA regulated No
Health authority Israel: Israeli Health Ministry Pharmaceutical Administration
Study type Interventional

Clinical Trial Summary

To look at the antihemmorhagic effect of 2 homeopathic drugs in women post delivery Bellis Perenis and Arnica montana


Description:

To look at the antihemmorhagic effect of 2 homeopathic drugs in women post delivery Bellis Perenis and Arnica montana compare it with placebo


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 210
Est. completion date September 2007
Est. primary completion date
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 18 Years and older
Eligibility Inclusion Criteria:

- healthy women during delivery

Exclusion Criteria:

- Scarred uterus, multifetal ,multiparty,bleeding problems,cesarean sectons,chorioamnionitis

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double-Blind, Primary Purpose: Prevention


Related Conditions & MeSH terms


Intervention

Drug:
Bellis Perenis ,Arnica montana


Locations

Country Name City State
Israel Haddasah Medical Organization Jerusalem

Sponsors (2)

Lead Sponsor Collaborator
Hadassah Medical Organization Shaare Zedek Medical Center

Country where clinical trial is conducted

Israel, 

References & Publications (1)

Oberbaum M, Galoyan N, Lerner-Geva L, Singer SR, Grisaru S, Shashar D, Samueloff A. The effect of the homeopathic remedies Arnica montana and Bellis perennis on mild postpartum bleeding--a randomized, double-blind, placebo-controlled study--preliminary re — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary hemoglobin levels 2 days post partum
Secondary pain
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