Optimizing the treatment of cystitis using nitrofurantoi

Recruiting

• Conditions: Urinary tract infection; bacterial infection; 10046590

• Registration Number: NL-OMON50420
• Lead Sponsor: Erasmus MC, Universitair Medisch Centrum Rotterdam

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Last Update Posted: 15 April 2024

Recruitment & Eligibility

• Status: Recruiting
• Sex: Not specified
• Target Recruitment: 60

Inclusion Criteria

1. Patients having been prescribed nitrofurantoin by treating physician because
suspicion of or proven urinary tract infection.
2. Age of at least 18 years.
3. Female sex
4. Glomerular filtration rate (GFR) greater than or equal to 30 ml/min based on
creatinine clearance.
5. Written informed consent by patient or legal representative

Exclusion Criteria

1. Treated with any antibiotics within 1 week of potential sampling period.
2. Known porphyria
3. Known allergic reaction or anaphylactic shock as a result of the consumption
of nitrofurantoin

Study & Design

• Study Type: Observational invasive
• Study Design: Not specified