Study on the Effectiveness and Safety of Cefepime/Nacubactam and Aztreonam/Nacubactam for Adults with Complicated Urinary Tract Infections or Acute Pyelonephritis

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What is this study about?

This clinical trial is focused on studying the treatment of complicated urinary tract infections (cUTI) and acute uncomplicated pyelonephritis (AP) in adults. These are types of infections that affect the urinary system, which includes the kidneys, bladder, and the tubes that connect them. The study will compare the effectiveness and safety of two different treatment combinations: cefepime/nacubactam and aztreonam/nacubactam, against another treatment called imipenem/cilastatin. All these medications are given through an intravenous (IV) infusion, which means they are administered directly into a vein.

The purpose of the study is to evaluate how well these treatments work and how safe they are for patients with these infections. Participants in the study will receive one of the treatment combinations or a placebo, and their progress will be monitored over a period of time. The study will involve regular visits to the clinic for check-ups and assessments to see how the infection is responding to the treatment. The goal is to find out which treatment is most effective in curing the infection and preventing it from coming back.

Throughout the study, participants will be closely observed to ensure their safety and to monitor any side effects that may occur. The study aims to provide valuable information that could help improve the treatment of these types of infections in the future. By comparing the different treatment options, researchers hope to identify the best approach for managing cUTI and AP, ultimately leading to better outcomes for patients.

1 joining the study

Upon joining the study, eligibility is confirmed based on criteria such as age, weight, and the need for intravenous antibiotics for at least 5 days.

The study focuses on treating complicated urinary tract infections (cUTI) or acute uncomplicated pyelonephritis (AP).

2 treatment assignment

Participants are randomly assigned to receive either cefepime/nacubactam, aztreonam/nacubactam, or imipenem/cilastatin.

All medications are administered through intravenous infusion.

3 medication administration

The treatment involves receiving the assigned medication intravenously. The specific dosage and frequency are determined by the study protocol.

The duration of the treatment is based on the medical condition and response to the medication.

4 monitoring and assessments

Throughout the treatment period, regular monitoring and assessments are conducted to evaluate the effectiveness and safety of the medication.

These assessments include clinical evaluations and laboratory tests to track progress and any side effects.

5 test of cure visit

A visit is scheduled to determine the success of the treatment, known as the Test of Cure (TOC) visit.

Success is measured by the resolution of symptoms and the eradication of the infection.

6 follow-up period

After the treatment, a follow-up period is conducted to ensure the infection does not return and to monitor for any delayed side effects.

Additional visits may be scheduled to assess long-term outcomes.

Who Can Join the Study?

Patients must be male or female and 18 years or older. This means they must be adults or at the age of legal consent.
Patients must weigh 140 kg or less. This is about 308 pounds.
The doctor must believe that the patient’s complicated urinary tract infection (cUTI) or acute uncomplicated pyelonephritis (AP) will need treatment with at least 5 days of intravenous (IV) antibiotics. Intravenous means the medicine is given directly into a vein.

Who Cannot Join the Study?

Patients who have a history of severe allergic reactions to any of the study medications.
Patients with a known allergy to beta-lactam antibiotics, which include penicillins and cephalosporins.
Patients who have a history of liver disease or liver problems.
Patients with kidney problems that require dialysis.
Patients who are pregnant or breastfeeding.
Patients who have participated in another clinical trial within the last 30 days.
Patients with a history of drug or alcohol abuse.
Patients who have a condition that, in the opinion of the study doctor, would make it unsafe for them to participate.

Where you can join this trial?

Verified and Recommended Sites

No sites found in this category

Verified Sites

Site Name	City	Country	Status
Acibadem City Clinic Diagnostic And Consultation Center Tokuda EAD	Sofia	Bulgaria

Other Sites

Site Name	City	Country
Fakultni Nemocnice Hradec Kralove	Novy Hradec Kralove	Czechia
Louna-Eesti Haigla AS	Voru	Estonia
Uyqxrbjtyq Mnohwyiagvfq Hrnacvle Fph Akqlfw Tylpqhawl Azy Ehsowveaa Mvgwmszv N I Puugwfs	Sofia	Bulgaria
Djjdrrhowsfjyxyajtgtrfp coxuri “gudcmugjcbhuiuf Ebbx	Sofia	Bulgaria
Nunsn Eipzurm Malmffq Cbictv Fousxwyqio	Tallin	Estonia
Pmfbx Sfquwtvk Cmuxwhfi Urwrvvjuow Hafcglpf	Riga	Latvia
Vboavkba mjycma kqnbypubs lclowhbi Vsbxh	Vilnius	Lithuania
Rwkfaaiknxgl Vjjtrikj ucidgvlwgaifhg lxxkuamq Vjrdo	Vilnius	Lithuania
Lqfdxwoe sgwodunmd mvhoip uvoikioraczs Kwika lkrgbjls	Kaunas	Lithuania
Fjhgucyh Tpmkarodgss nmvfzwilj	Prague	Czechia
Kcdeceb natprahso Lfjoyjz ahjr	Liberec	Czechia
Taaot Uwlrfagltm Hpfroyrc	Tartu	Estonia
Rbujs Aimhidob kcilldiy uxgtxocjwpuma svyoqzyr Slx	Riga	Latvia
Lswzaszagytasr Kysjhcjbdc Ax	Pohja-Tallinna Linnaosa	Estonia
Vpfzkuua Scwckpty Ssz	Valmiera	Latvia
Lzyxboaq sahxjoyjz mdbuzr uslsjuvxcxea lhelvyld Kefca klyayujb	Kaunas	Lithuania
Kasagdt znsqwgogu aguv	Teplice	Czechia
Swvvcqglpi Iunxxqdf Kbwxadbjjb	Kohtla-Jarve Linn	Estonia
Uynjtyysji Muqftkqhegzhkccqo Hgfwsojp Fgv Amxclf Tfosnxffg Klydf Aq	Ruse	Bulgaria
Amci Hmajlpiu Gqivqhi Lb Squxtzh Sfojuab aboi	Svidnik	Slovakia
Mhvtwzgulhzte Hidnsydt fmw Azfure Trycudszn Hfbsu ack Bdnax Epg	Pleven	Bulgaria
Nrfvqrcgm S Pwtselzyefda Sm Lswfzq Gnolotb aisj	Galanta	Slovakia
Ptbvn Hsrpyvqry Sl agaa	Rimavska Sobota	Slovakia
Mwocwmfrldmu Hptvppmj Fvu Amryen Ttlqvoiev Sfaivoou Ao	Silistra	Bulgaria

Trial status

Country	Status	Recruitment Start
Bulgaria	Not recruiting	22.05.2023
Czechia	Not recruiting	22.05.2023
Estonia	Not recruiting	22.05.2023
Latvia	Not recruiting	22.05.2023
Lithuania	Not recruiting	22.05.2023
Slovakia	Not recruiting	22.05.2023

Trial locations

Investigated Drugs:

Cefepime/Nacubactam is a combination medication used in this study to treat complicated urinary tract infections or acute uncomplicated kidney infections. Cefepime is an antibiotic that helps kill bacteria, while Nacubactam enhances the effectiveness of Cefepime by preventing bacteria from breaking it down.

Aztreonam/Nacubactam is another combination medication being tested in the trial. Aztreonam is an antibiotic that targets and kills bacteria, and Nacubactam is included to boost the antibiotic’s effectiveness by protecting it from bacterial resistance mechanisms.

Imipenem/Cilastatin is a standard treatment used as a comparison in this study. Imipenem is a powerful antibiotic that fights a wide range of bacteria, and Cilastatin is added to prevent the breakdown of Imipenem in the kidneys, ensuring it remains effective in treating infections.

Investigated Diseases:

Complicated Urinary Tract Infection (cUTI) – This condition involves infections of the urinary tract that occur in the presence of an underlying complicating factor, such as a structural or functional abnormality of the urinary tract. It can affect the bladder, kidneys, or both, and is often caused by bacteria. Symptoms may include frequent urination, pain during urination, and abdominal pain. The infection can progress to involve the kidneys, leading to more severe symptoms. It is more challenging to treat than uncomplicated urinary tract infections due to these complicating factors.

Acute Uncomplicated Pyelonephritis (AP) – This is a sudden and severe kidney infection that typically results from bacteria traveling from the bladder to the kidneys. It is characterized by symptoms such as fever, chills, back or side pain, and nausea. The condition primarily affects healthy individuals without structural or functional abnormalities of the urinary tract. If not addressed, it can lead to more severe kidney involvement. The infection is usually caused by common bacteria found in the urinary tract.

Trial ID:

2024-515463-55-00

Protocol code:

OP0595-5

NCT ID:

NCT05887908

Trial Phase:

Therapeutic confirmatory (Phase III)

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Study on the Effectiveness and Safety of Cefepime/Nacubactam and Aztreonam/Nacubactam for Adults with Complicated Urinary Tract Infections or Acute Pyelonephritis

What is this study about?

Who Can Join the Study?

Who Cannot Join the Study?