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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT03736187
Other study ID # Antibiotics for SSI
Secondary ID
Status Not yet recruiting
Phase N/A
First received
Last updated
Start date April 2019
Est. completion date December 2019

Study information

Verified date November 2018
Source Ain Shams University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Effect of cephalexin plus metronidazole on SSI better than cephalexin alone in obese women undergoing CS


Description:

Comparison between efficacy of cephalexin alone and cephalexin plus metronidazole on surgical site infection in obese women undergoing CS and follow up of any signs of wound infection


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 280
Est. completion date December 2019
Est. primary completion date October 2019
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group N/A and older
Eligibility Inclusion Criteria:

- obese women under elective CS

Exclusion Criteria:

- immunodeficient women

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Cephalexin
Giving cephalexin and metronidazole in one group &cephalexin alone in another group

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Ain Shams University

Outcome

Type Measure Description Time frame Safety issue
Primary Wound infection Fever, redness, ecchymosis and tenderness One week
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