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Urine pH and Urinary Tract Infection (PHURINE)

V

Vaud University Hospital Center

Status

Unknown

Conditions

Urinary Stone
Urinary Tract Infections

Study type

Observational

Funder types

Other

Identifiers

NCT04598971
2020-00779

Details and patient eligibility

About

Urinary tract infections (UTI) affect the urine pH and may lead to salt precipitation such as struvite. Bacteria with urease activity are known to alkalinise urine, but not much is known on how pH is changing over time during UTI.

This study aims at following urine pH progression at the time of diagnosis of UTI and during the treatment phase.

Description of the change in urine pH over time will help understanding the risk of struvite formation and potential timing of intervention.

Full description

Adults presenting with UTI symptoms will be screened for infection and instructed to monitor urine pH during the course of treatment and 1 week after. Urine pH will be measured by the patients using calibrated pH-stix. Type of bacteria, antibiotics, and the type of diet will be monitored during the study.

Enrollment

50 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion and exclusion criteria

Group 1. Cystitis

Inclusion Criteria:

  • Symptoms of dysuria, pollakiuria, no fever AND
  • urine-stix positive for leucocytes OR positive culture (>10E5 cfu/ml)

Group 2. Pyelonephritis

Inclusion Criteria:

  • Unilateral flank pain, pollakiuria, dysuria, fever (>38.5°C) AND
  • urine-stix positive for leucocytes OR positive culture (>10E5 cfu/ml)

Exclusion Criteria (both groups):

  • known urinary tract anatomic abnormalities
  • Presence of a urine catheter
  • Sepsis - septic shock
  • Patient taking drug interfering with urine pH (diuretics, citrate, acetazolamide, topiramate,...)
  • Patients with UTI diagnosed in the preceding month
  • Patients having received antibiotics during the preceding month
  • Male patient with a diagnosis of prostatitis
  • Presence of infected kidney cyst
  • Patient with diabetes
  • Pregnant female
  • Patient with obstructive pyelonephritis

Trial design

50 participants in 2 patient groups

Cystitis
Description:
Patients with lower UTI will be included in this group
Pyelonephritis
Description:
Patients with higher UTI will be included in this group

Trial contacts and locations

1

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Central trial contact

Charlotte Desponds, BM; Alexandre Gouveia, MD

Data sourced from clinicaltrials.gov

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