Clinical Trial Comparing Oral Versus Intravenous Cefuroxime in Pregnant Women with Pyelonephritis (CEFURO)

Hospital de Clinicas de Porto Alegre

Status and phase: Enrolling; Phase 4

Conditions: Pyelonephritis in Pregnancy

Treatments: Drug: Cefuroxime Axetil; Drug: Cefuroxime

Study type: Interventional

Funder types: Other

Identifiers

NCT06527560

2024-0118

Details and patient eligibility

About

The goal of this clinical trial is to compare rates of cure in pregnant women with pyelonephritis. The main question aims to answer:

Can we treat pyelonephritis in pregnancy with oral cefuroxime alone?

Pregnant women with pyelonephritis treated with intravenous cefuroxime will be the comparator.

Participants will be asked to accept participation in the study and will be randomly allocated to one of the two arms:

• Intravenous cefuroxime 750 mg every 8 hours + oral placebo every 12 hours
• Oral cefuroxime 500 mg every 12 hours + intravenous saline solution every 8 hours

Full description

Urinary tract infections are common during pregnancy and can lead to pyelonephritis, a condition associated with morbidity in both the fetus and the pregnant woman. At HCPA, intravenous cefuroxime has been used until the antibiogram results from the pregnant woman's urine culture are available. However, this treatment requires hospitalization, which is financially burdensome and can affect the well-being of the pregnant woman. Despite this, there are not enough studies to investigate the use of oral cefuroxime as an initial treatment.

Objective: To compare the efficacy of cefuroxime administered orally versus intravenously in curing pyelonephritis during pregnancy, aiming to test the non-inferiority of the oral treatment.

Method: A randomized, prospective, triple-blind, two-arm study will be conducted. Pregnant women with pyelonephritis who agree to participate in the study at the time of hospitalization will receive the treatment: I) cefuroxime axetil 750mg IV every 8 hours and a placebo capsule 500mg; or II) 500mg orally every 12 hours and IV saline solution. These patients will be followed until the outcome is determined. After 48 hours in good clinical condition, the patients will be discharged and will continue treatment with cefuroxime axetil 500mg orally every 12 hours for 14 days. To analyze the difference in means and proportions with confidence intervals, Student's t-test will be performed, while nominal data will be analyzed using the chi-square test.

Enrollment: 100 estimated patients

Sex: Female

Ages: 18 to 48 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Pregnant women aged 18 years or older and less than 20 weeks of gestational age, determined by ultrasound or the date of last menstruation, who come to the HCPA emergency department with a clinical diagnosis of pyelonephritis in pregnancy, defined as:
• Presence of lower back pain associated with
• Dysuria with leukocyturia, or hematuria or nitrite in the urine test with at least one of the criteria below:
• Leukocytosis (> 14,000 leukocytes/mL)
• Warm extremities, thready pulse, and tachycardia (HR > 110 bpm)
• Cyanosis and/or pallor
• Tachypnea (RR > 30 breaths/min)
• Arterial hypotension (SBP < 90mmHg)
• Positive costovertebral angle tenderness
• Urine culture with colony growth
• Hyperthermia (≥ 37.8°C)"

Exclusion criteria

• Do not wish to participate in the project.

• Used antimicrobials prior to hospitalization (3-day period).

• those who are allergic to cefuroxime.

• Have a urine culture antibiogram resistant to cefuroxime AND absence of clinical improvement (in this case, will be excluded as modified intention to treat).

• Have a diagnosis other than pyelonephritis, for example, appendicitis.

• those in septic shock, defined as:

  • the need for vasopressor to maintain a mean arterial pressure ≥ 65 mmHg and lactate > 2 mmol/l or 2 points on qSOFA. qSOFA will be considered positive when at least two of the following clinical criteria are present:
  • Respiratory rate greater than or equal to 22 breaths per minute;
  • Altered level of consciousness (Glasgow Coma Scale score less than 15);
  • Systolic blood pressure less than or equal to 100 mmHg.

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Triple Blind

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100 participants in 2 patient groups

Intravenous cefuroxime

Active Comparator group

Description:

Intravenous cefuroxime 750 mg every 8 hours + oral placebo every 12 hours

Treatment:

Drug: Cefuroxime

Oral axetil cefuroxime

Experimental group

Description:

Oral axetil cefuroxime 500 mg every 12 hours + intravenous saline solution every 8 hours

Treatment:

Drug: Cefuroxime Axetil