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Spots Global Cancer Trial Database for Does Cefoxitin or Piperacillin-Tazobactam Prevent Postoperative Surgical Site Infections After Pancreatoduodenectomy?

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Trial Identification

Brief Title: Does Cefoxitin or Piperacillin-Tazobactam Prevent Postoperative Surgical Site Infections After Pancreatoduodenectomy?

Official Title: A Phase III Multicenter, Open Label Randomized Controlled Trial of Cefoxitin Versus Piperacillin-Tazobactam as Surgical Antibiotic Prophylaxis in Patients Undergoing Pancreatoduodenectomy

Study ID: NCT03269994

Study Description

Brief Summary: The purpose of this study is to figure out which commonly used antibiotic, cefoxitin or piperacillin-tazobactam, is better at decreasing the rate of surgical site infections after pancreatoduodenectomy.

Detailed Description:

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

UC Davis Comprehensive Cancer Center, Sacramento, California, United States

Emory University School of Medicine, Atlanta, Georgia, United States

Northwestern Medicine (Data Collection), Chicago, Illinois, United States

NorthShore University Health System, Evanston, Illinois, United States

Indiana University, Indianapolis, Indiana, United States

University of Iowa, Iowa City, Iowa, United States

Massachusetts General Hospital, Boston, Massachusetts, United States

University of Washington School of Medicine, Saint Louis, Missouri, United States

University of Nebraska Medical Center, Omaha, Nebraska, United States

Memorial Sloan Kettering Basking Ridge (Consent only), Basking Ridge, New Jersey, United States

Hackensack Meridian Health / Hackensack University Medical Center Cancer Center, Hackensack, New Jersey, United States

Montefiore Health Systems (Montefiore Medical Center), Bronx, New York, United States

Memorial Sloan Kettering Commack (Consent only), Commack, New York, United States

Memoral Sloan Kettering Westchester (Consent only), Harrison, New York, United States

Mount Sinai Hospital, New York, New York, United States

Mount Sinai West, New York, New York, United States

Memorial Sloan Kettering Cancer Center, New York, New York, United States

Duke University, Durham, North Carolina, United States

Brody School of Medicine at East Carolina University, Greenville, North Carolina, United States

Ohio State University, Columbus, Ohio, United States

Providence Health & Services (Portland Med Ctr), Portland, Oregon, United States

Pennsylvania State Hershey, Hershey, Pennsylvania, United States

Thomas Jefferson University Hospital, Philadelphia, Pennsylvania, United States

Baptist Memorial Healthcare, Memphis, Tennessee, United States

Baylor Scott & White Health, Dallas, Texas, United States

Intermountain Healthcare, Murray, Utah, United States

University of Utah, Salt Lake City, Utah, United States

Gundersen Lutheran Medical Foundation, La Crosse, Wisconsin, United States

University of Wisconsin, Madison, Wisconsin, United States

Hamilton Health Sciences Center (Juravinski Hospital), Hamilton, Ontario, Canada

Ottawa Hospital, Ottawa, Ontario, Canada

Sunnybrook Health Sciences Centre, Toronto, Ontario, Canada

Contact Details

Name: Michael D'Angelica, MD

Affiliation: Memorial Sloan Kettering Cancer Center

Role: PRINCIPAL_INVESTIGATOR

Useful links and downloads for this trial

Clinicaltrials.gov

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