Does Additional Use of Preoperative Azithromycin Decrease Posthysterectomy Infections
Launched by HELSINKI UNIVERSITY CENTRAL HOSPITAL · Apr 14, 2022
Trial Information
Current as of June 26, 2025
Recruiting
Keywords
ClinConnect Summary
This clinical trial is looking at whether taking an additional antibiotic called azithromycin before surgery can help reduce the risk of infections after a hysterectomy, which is the surgical removal of the uterus. During this surgery, bacteria can enter the body and potentially lead to infections, affecting about 5% of women who undergo the procedure. The study aims to find out if giving azithromycin, along with a commonly used antibiotic called cefuroxime, can lower the chances of infections compared to using cefuroxime alone. Researchers will also explore if this approach impacts other types of infections and any side effects that might arise.
To participate in this trial, women aged 65 to 74 who are having a hysterectomy for non-cancerous reasons at specific hospitals in Finland may be eligible, as long as they don’t have any allergies to the study medications or certain heart conditions. Participants will be asked questions about their health and will undergo a heart test before being enrolled. This study not only aims to improve patient care by reducing infections but also hopes to understand more about factors like bacterial infections and the body’s natural bacteria after surgery.
Gender
FEMALE
Eligibility criteria
- Inclusion Criteria:
- • Women undergoing hysterectomy for benign indication in University Hospitals (Helsinki University Hospital, Turku University Hospital, Tampere University Hospital, Oulu University Hospital and Kuopio University Hospital) who have not any contraindications for azithromycin or cefuroxime.
- Exclusion Criteria:
- • Inability to understand the study protocol.
- • Allergy for either cefuroxime or azithromycin.
- • Congenital or acquired prolonged Q-T-corrected interval. All the participants will be asked about arrhythmias and whether they have congenital arrhythmias in the family,
- • Electrocardiogram will be checked for all the participants.
- • Use of medicines that may prolong Q-T-corrected interval (class Ia arrhythmia medications, quinidine, procainamide, and class III arrhythmia medications dofetilide, amiodarone and sotalol).
- • Use of selective serotonin reuptake inhibitor medication and prolonged Q-T-corrected interval.
About Helsinki University Central Hospital
Helsinki University Central Hospital (HUCH) is a leading academic medical institution in Finland, dedicated to advancing healthcare through innovative research and clinical excellence. As a pivotal sponsor of clinical trials, HUCH integrates cutting-edge medical practices with rigorous scientific inquiry, fostering collaborations between researchers, healthcare professionals, and patients. The hospital is committed to enhancing patient outcomes and contributing to the global body of medical knowledge by conducting high-quality, ethically sound clinical studies across a diverse range of therapeutic areas. With a strong emphasis on education and training, HUCH plays a vital role in shaping the next generation of healthcare leaders and researchers.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Helsinki, , Finland
Turku, , Finland
Tampere, , Finland
Jyväskylä, , Finland
Kuopio, , Finland
Oulu, , Finland
Patients applied
Trial Officials
Päivi Rahkola-Soisalo, Adj prof, MD
Principal Investigator
Helsinki University Central Hospital
Tomi Mikkola, Prof, MD
Study Chair
Helsinki University Central Hospital
Päivi Rahkola-Soisalo, Adj prof, MD
Study Director
Helsinki University Central Hospital
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported
Similar Trials