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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT00391599
Other study ID # OS-SL-002
Secondary ID
Status Not yet recruiting
Phase Phase 2
First received October 22, 2006
Last updated August 6, 2007

Study information

Verified date June 2006
Source Wolfson Medical Center
Contact n/a
Is FDA regulated No
Health authority Israel: Ministry of Health
Study type Interventional

Clinical Trial Summary

Enemas are not anymore used routinely before vaginal deliveries.The intention of this study is to elucidate whether there is a benefit in routine use of enema before cesarean section.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 0
Est. completion date
Est. primary completion date
Accepts healthy volunteers No
Gender Female
Age group 18 Years to 50 Years
Eligibility Inclusion Criteria:

- Cesarean Section, Elective

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Supportive Care


Related Conditions & MeSH terms

  • Complications After Cesarean Section

Intervention

Procedure:
enema


Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Wolfson Medical Center