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Treating Pyelonephritis an Urosepsis With Pivmecillinam (MePUr)

Primary Purpose

Pyelonephritis, Urinary Tract Infections

Status
Completed
Phase
Phase 4
Locations
Norway
Study Type
Interventional
Intervention
pivmecillinam
Sponsored by
Sykehuset i Vestfold HF
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Pyelonephritis focused on measuring Pivmecillinam

Eligibility Criteria

18 Years - 110 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • E.coli in blood culture
  • AND identical isolate in urine sample (>= 1.000 CFU) OR relevant clinical signs of UTI

Exclusion Criteria:

  • Bacterial infection origin from another organ (e.g. pneumonia)
  • Severe sepsis with multiorgan failure
  • Perinephritic abscess
  • Pyonephrosis requiring drainage
  • Allergy to pivmecillinam
  • E.coli isolate resistant to pivmecillinam
  • Pregnancy/breastfeeding
  • Severe neutropenia
  • Prostatitis
  • Severe kidney failure (eGFR<15 ml/min)
  • Using valproate

Sites / Locations

  • Vestfold Hospital Trust

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Pivmecillinam

Arm Description

Patients treated with pivmecillinam

Outcomes

Primary Outcome Measures

Clinical efficacy
Defined as abscence of fever, no need for other antibiotics than prescribed and improvement of symptoms (self-reported improvement and EQ 5D VAS-scale).

Secondary Outcome Measures

C-reactive protein-level (CRP)
Compare CRP-level on day 0 with day 17.
Readmission due to urinary tract infection (UTI)
Check if participants are readmitted due to UTI.
Readmission - any cause
Check if participants have been readmitted to hospital
Adverse effects
Registrate frequency of rash/skin problems, abdominal pain, clostridium difficile associated diarrhea
Microbial efficacy
Defined as <1.000 CFU E.coli in urine

Full Information

First Posted
April 25, 2017
Last Updated
April 21, 2020
Sponsor
Sykehuset i Vestfold HF
Collaborators
University of Oslo
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1. Study Identification

Unique Protocol Identification Number
NCT03282006
Brief Title
Treating Pyelonephritis an Urosepsis With Pivmecillinam
Acronym
MePUr
Official Title
The Efficacy and Safety of Pivmecillinam in Treating Bacteriemic Urosepsis Caused by E.Coli
Study Type
Interventional

2. Study Status

Record Verification Date
April 2020
Overall Recruitment Status
Completed
Study Start Date
September 29, 2017 (Actual)
Primary Completion Date
April 21, 2020 (Actual)
Study Completion Date
April 21, 2020 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Sykehuset i Vestfold HF
Collaborators
University of Oslo

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Febrile urinary tract infections and urosepsis are common and potentially serious infections that require effective antimicrobial treatment. The duration of parenteral treatment depends on oral alternatives. These alternatives are few and due to antimicrobial resistance, quinolones are "standard of care". The increased use of quinolones is concerning because of its negative ecological aspects and it is confirmed an increasing incidence of resistant E.coli to quinolones in Norwegian isolates. Pivmecillinam is an antibiotic with high susceptibility to E.coli but the evidence for treating febrile urinary tract infections is insufficient. This trial will investigate the efficacy and safety of pivmecillinam in treating pyelonephritis and urosepsis caused by E.coli. The hypothesis is that urosepsis can safely be treated with pivmecillinam when it is given after 2-3 days with empirical i.v. antibiotics.
Detailed Description
This trial will be conducted at Vestfold Hospital, Norway, and is a prospective observational study with intention to treat. Participants will be consecutively included among hospitalized patients suffering from urosepsis - see eligibility criteria. After 3 days with parenteral antibiotics, when clinical improvement and absence of fever/leukocytosis is confirmed, the participants will start on pivmecillinam 400mg four times daily and be discharged. Pivmecillinam is to be taken for one week. The participants will be contacted by phone on day 4, 10 and 33 (days after admission). On day 17 (test of cure, TOC) they will meet for physical examination. They will report symptom score (standardized schema) on day 0, and 17. Urine samples will be collected on day 10 and 17. Blood samples on day 17. All data will be stored anonymously. The trial will be monitored by extern resources.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Pyelonephritis, Urinary Tract Infections
Keywords
Pivmecillinam

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
53 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Pivmecillinam
Arm Type
Experimental
Arm Description
Patients treated with pivmecillinam
Intervention Type
Drug
Intervention Name(s)
pivmecillinam
Other Intervention Name(s)
Selexid, Penomax
Intervention Description
Oral treatment of bacteremic pyelonephritis following standard initial parenteral treatment
Primary Outcome Measure Information:
Title
Clinical efficacy
Description
Defined as abscence of fever, no need for other antibiotics than prescribed and improvement of symptoms (self-reported improvement and EQ 5D VAS-scale).
Time Frame
Day 17
Secondary Outcome Measure Information:
Title
C-reactive protein-level (CRP)
Description
Compare CRP-level on day 0 with day 17.
Time Frame
Day 17
Title
Readmission due to urinary tract infection (UTI)
Description
Check if participants are readmitted due to UTI.
Time Frame
Day 33
Title
Readmission - any cause
Description
Check if participants have been readmitted to hospital
Time Frame
Day 33
Title
Adverse effects
Description
Registrate frequency of rash/skin problems, abdominal pain, clostridium difficile associated diarrhea
Time Frame
Day 33
Title
Microbial efficacy
Description
Defined as <1.000 CFU E.coli in urine
Time Frame
Day 17

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
110 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: E.coli in blood culture AND identical isolate in urine sample (>= 1.000 CFU) OR relevant clinical signs of UTI Exclusion Criteria: Bacterial infection origin from another organ (e.g. pneumonia) Severe sepsis with multiorgan failure Perinephritic abscess Pyonephrosis requiring drainage Allergy to pivmecillinam E.coli isolate resistant to pivmecillinam Pregnancy/breastfeeding Severe neutropenia Prostatitis Severe kidney failure (eGFR<15 ml/min) Using valproate
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Tore Stenstad, MD, PhD
Organizational Affiliation
The Hospital of Vestfold
Official's Role
Principal Investigator
Facility Information:
Facility Name
Vestfold Hospital Trust
City
Tønsberg
State/Province
Vestfold
ZIP/Postal Code
3103
Country
Norway

12. IPD Sharing Statement

Citations:
PubMed Identifier
35590284
Citation
Hansen BA, Grude N, Lindbaek M, Stenstad T. The efficacy of pivmecillinam in oral step-down treatment in hospitalised patients with E. coli bacteremic urinary tract infection; a single-arm, uncontrolled treatment study. BMC Infect Dis. 2022 May 19;22(1):478. doi: 10.1186/s12879-022-07463-7.
Results Reference
derived

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Treating Pyelonephritis an Urosepsis With Pivmecillinam

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