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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT00353236
Other study ID # SHEBA-06-4170-JK-CTIL
Secondary ID
Status Recruiting
Phase N/A
First received July 17, 2006
Last updated July 17, 2006

Study information

Verified date July 2006
Source Sheba Medical Center
Contact Jacob kuint, MD
Phone 972-3-5303030
Email kuint-j@sheba.health.gov.il
Is FDA regulated No
Health authority Israel: Israeli Health Ministry Pharmaceutical Administration
Study type Observational

Clinical Trial Summary

Delivery of twins or preterm infant is a very stressful episode to mothers. The purpose of this study is to characterize maternal psychological resources in dealing with this situation and compare it to mothers giving birth to singleton at term


Recruitment information / eligibility

Status Recruiting
Enrollment 0
Est. completion date
Est. primary completion date
Accepts healthy volunteers No
Gender Both
Age group N/A and older
Eligibility Inclusion Criteria:

- Study group: Mothers who give birth to twins or preterm infants

- Control: Mothers who give birth to singleton, full term infants

Exclusion Criteria:

Study Design

Observational Model: Case Control, Time Perspective: Longitudinal


Related Conditions & MeSH terms


Locations

Country Name City State
Israel Sheba Medical Center - Neonatal Department Ramat -Gan

Sponsors (1)

Lead Sponsor Collaborator
Sheba Medical Center

Country where clinical trial is conducted

Israel, 

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