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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT03007706
Other study ID # MiniaMUH
Secondary ID
Status Not yet recruiting
Phase N/A
First received December 29, 2016
Last updated December 30, 2016
Start date January 2017
Est. completion date October 2017

Study information

Verified date December 2016
Source Minia Maternity University Hospital
Contact n/a
Is FDA regulated No
Health authority Egypt : Minia maternity university hospital
Study type Observational [Patient Registry]

Clinical Trial Summary

This study aims to determine the effectiveness of skin cleansing and prophylactic antibiotics given to women undergoing a cesarean section for reducing the incidence of postpartum infectious morbidity and to assess potential maternal adverse effects and any impact on the infant.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 200
Est. completion date October 2017
Est. primary completion date June 2017
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 18 Years to 45 Years
Eligibility Inclusion Criteria:

1. Women undergoing cesarean delivery, both elective and non-elective.

2. Rupture of membranes and labor contractions will be allowed.

Exclusion Criteria:

1. Unknown outcome from the patient.

2. Refusing to participate in the study from the admission conse

3. Allergy to antibiotics.

4. Any visible infection.

Study Design

Observational Model: Case-Only, Time Perspective: Prospective


Related Conditions & MeSH terms


Intervention

Procedure:
Women undergo cesarean section delivery


Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Raghda Gamal Mohamed

Outcome

Type Measure Description Time frame Safety issue
Primary role of skin cleansing and prophylactic antibiotics given to women undergoing a cesarean section for reducing the incidence of postpartum infectious morbidity 2 weeks following cesarean section Yes