Minia University Hospital
Minya, Egypt
Location status: Recruiting
Location contact
asmaa Elsayed, Ph.D.
CONTACT
NCT Number: NCT06607887
Comparison between postoperative parenteral prophylactic antibiotics, and oral antibiotics regarding the incidence of post laparoscopic cholecystectomy infection.
Interested in participating?
Request Info18 year and older
All sexes
Interventional
Phase 4
Minya, Egypt
Location status: Recruiting
asmaa Elsayed, Ph.D.
CONTACT
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Parenteral prophylactic antibiotics (cefazolin), 1st dose at the time of induction of anesthesia, 2nd dose after 12hs from the surgery.
Parenteral prophylactic antibiotic (cefazolin), dose at the time of induction of anesthesia and then oral antibiotic for five days postoperative.
Time frame: 4 weeks
DSSI = deep surgical site infection; SSSI = superficial surgical site infection.
Time frame: 4 weeks
Time frame: 4 weeks
Time frame: 4 weeks
Contact information is provided by the study sponsor or research team.
Minia University Hospital
Other
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
Published trials that share one or more normalized conditions with this study.
NCT05153694
Bacterial Infections, Bacterial Infections and Mycoses
Munich, Outside U.S./Canada, Germany
View Trial DetailsNCT04192435
Anesthesia, Bleeding
Melbourne, Victoria, Australia
View Trial DetailsNCT04753723
Burn Wound, Burns
San Antonio, Texas, United States
View Trial DetailsNCT04516148
Burn, Burns
Washington D.C., District of Columbia, United States
View Trial Details