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N/A Completed N=10

Portable Pves Study

Source: ClinicalTrials.gov NCT02673944 ↗
Enrolled (actual)
10
Serious AEs
0.0%
Results posted
Jun 2016
Primary outcomePrimary: Accurate Vesical PRessure — 18.56; 17.45 cm H2O

Summary

A comparative study will be conducted and the patient will undergo a conventional urodynamic study. In order to successfully determine if the Peritron+ is capturing vesical pressure measurements consistent with conventional urodynamics the two sources of Pves will be collected concurrently.

Outcome Measures

OutcomeResultp-value
PRIMARY
Accurate Vesical PRessure
18.56; 17.45

Eligibility Criteria

Inclusion Criteria

  • Patients normally indicated for urodynamic evaluation

Exclusion Criteria

  • Patients who suffer from bladder infections
  • Patients who suffer from strictures in the urethra
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT02673944). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication. Informational only — not medical advice.

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