Page last updated: 2024-10-31

metronidazole and Necrotizing Pyelonephritis

metronidazole has been researched along with Necrotizing Pyelonephritis in 6 studies

Metronidazole: A nitroimidazole used to treat AMEBIASIS; VAGINITIS; TRICHOMONAS INFECTIONS; GIARDIASIS; ANAEROBIC BACTERIA; and TREPONEMAL INFECTIONS.
metronidazole : A member of the class of imidazoles substituted at C-1, -2 and -5 with 2-hydroxyethyl, nitro and methyl groups respectively. It has activity against anaerobic bacteria and protozoa, and has a radiosensitising effect on hypoxic tumour cells. It may be given by mouth in tablets, or as the benzoate in an oral suspension. The hydrochloride salt can be used in intravenous infusions. Metronidazole is a prodrug and is selective for anaerobic bacteria due to their ability to intracellularly reduce the nitro group of metronidazole to give nitroso-containing intermediates. These can covalently bind to DNA, disrupting its helical structure, inducing DNA strand breaks and inhibiting bacterial nucleic acid synthesis, ultimately resulting in bacterial cell death.

Research Excerpts

ExcerptRelevanceReference
" Ceftolozane/tazobactam is an antibacterial with potent activity against Gram-negative pathogens and is approved for the treatment of cIAI (with metronidazole) and cUTI (including pyelonephritis)."5.24Analysis of patients with diabetes and complicated intra-abdominal infection or complicated urinary tract infection in phase 3 trials of ceftolozane/tazobactam. ( Huntington, JA; Long, J; Popejoy, MW, 2017)

Research

Studies (6)

TimeframeStudies, this research(%)All Research%
pre-19902 (33.33)18.7374
1990's1 (16.67)18.2507
2000's0 (0.00)29.6817
2010's3 (50.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Popejoy, MW1
Long, J1
Huntington, JA1
Gupta, P1
Gupta, R2
Jandial, K1
Samotra, S1
Rana, V1
Gupta, S1
Singh, J1
Christodoulidou, M1
Thomas, M1
Sharma, SD1
DRAPER, JW1
AKBARI, A1
WARD, JN1
Pühse, G1
Roos, N1
Ludwig, K1
Hertle, L1
Ingham, HR1
Rich, GE1
Selkon, JB1
Hale, JH1
Roxby, CM1
Betty, MJ1
Johnson, RW1
Uldall, PR1

Clinical Trials (2)

Trial Overview

TrialPhaseEnrollmentStudy TypeStart DateStatus
A Multicenter, Double-Blind, Randomized, Phase 3 Study to Compare the Efficacy and Safety of Intravenous CXA-201 With That of Meropenem in Complicated Intraabdominal Infections[NCT01445678]Phase 3494 participants (Actual)Interventional2011-12-23Completed
A Multicenter, Double-Blind, Randomized, Phase 3 Study to Compare the Safety and Efficacy of Intravenous CXA-201 and Intravenous Levofloxacin in Complicated Urinary Tract Infection, Including Pyelonephritis[NCT01345929]Phase 3558 participants (Actual)Interventional2011-06-20Completed
[information is prepared from clinicaltrials.gov, extracted Sep-2024]

Trial Outcomes

The Percentage of Subjects With Clinical Outcome of Cure at the Test of Cure (TOC) Visit in the Microbiological Intent to Treat (MITT) Population

Clinical cure is complete resolution or significant improvement in signs and symptoms of the index infection, such that no additional antibacterial therapy or surgical or drainage procedure was required for the index infection. (NCT01445678)
Timeframe: TOC; 26-30 days after start of study drug administration

Interventionpercentage of subjects (Number)
CXA-201 and Metronidazole as Treatment for cIAI83.0
Meropenem as Treatment for cIAI87.3

The Percentage of Subjects With Clinical Response at End of Therapy (EOT) Visit in the MITT Population

Clinical response is complete resolution or significant improvement in signs and symptoms of the index infection, such that no additional antibacterial therapy or surgical or drainage procedure was required for the index infection. (NCT01445678)
Timeframe: EOT; Within 24 hours of last study drug administration

Interventionpercentage of subjects (Number)
CXA-201 and Metronidazole as Treatment for cIAI89.2
Meropenem as Treatment for cIAI92.3

The Percentage of Subjects With Clinical Response at End of Therapy in the ME Population

Clinical response is complete resolution or significant improvement in signs and symptoms of the index infection, such that no additional antibacterial therapy or surgical or drainage procedure was required for the index infection. (NCT01445678)
Timeframe: EOT; Within 24 hours of last study drug administration

Interventionpercentage of subjects (Number)
CXA-201 and Metronidazole as Treatment for cIAI97.1
Meropenem as Treatment for cIAI97.5

The Percentage of Subjects With Clinical Response at LFU Visit in the ME Population

Clinical response is clinical cure at TOC and no signs and symptoms recur or worsen since the TOC visit (NCT01445678)
Timeframe: LFU; 38 to 45 days after first study drug administration

Interventionpercentage of subjects (Number)
CXA-201 and Metronidazole as Treatment for cIAI100
Meropenem as Treatment for cIAI99.3

The Percentage of Subjects With Clinical Response at Long Term Follow-Up (LFU) in the MITT Population

Clinical response is clinical cure at TOC and no signs and symptoms recur or worsen since the TOC visit. (NCT01445678)
Timeframe: LFU; 38 to 45 days after first study drug administration

Interventionpercentage of subjects (Number)
CXA-201 and Metronidazole as Treatment for cIAI82.5
Meropenem as Treatment for cIAI86.6

The Percentage of Subjects With Microbiological Outcome of Success at the TOC Visit in the Microbiologically Evaluable (ME) Population

Success is eradication (absence of the baseline pathogen in a specimen appropriately obtained from the original site of infection) or presumed eradication (absence of material to culture in a subject who was assessed as a clinical cure) for each baseline pathogen (NCT01445678)
Timeframe: TOC; 26-30 days after start of study drug administration

Interventionpercentage of subjects (Number)
CXA-201 and Metronidazole as Treatment for cIAI94.2
Meropenem as Treatment for cIAI94.7

The Percentage of Subjects Who Have Both a Per-subject Microbiological Outcome of Eradication and a Clinical Outcome of Cure at the Test of Cure (TOC) Visit in the Microbiological Modified ITT (mMITT) Population

(NCT01345929)
Timeframe: Test of Cure Visit (7 Days [± 2 days] after completion of study drug administration)

Interventionpercentage of subjects (Number)
CXA-201 as Treatment for cUTI76.9
Levofloxacin as Treatment for cUTI68.4

The Percentage of Subjects Who Have Both a Per-subject Microbiological Outcome of Eradication and a Clinical Outcome of Cure at the TOC Visit in the Microbiologically Evaluable (ME) Population.

(NCT01345929)
Timeframe: Test of Cure Visit (7 Days [± 2 days] after completion of study drug administration)

Interventionpercentage of subjects (Number)
CXA-201 as Treatment for cUTI83.3
Levofloxacin as Treatment for cUTI75.4

Trials

1 trial available for metronidazole and Necrotizing Pyelonephritis

ArticleYear
Analysis of patients with diabetes and complicated intra-abdominal infection or complicated urinary tract infection in phase 3 trials of ceftolozane/tazobactam.
    BMC infectious diseases, 2017, 05-02, Volume: 17, Issue:1

    Topics: Adult; Aged; Anti-Bacterial Agents; Bacterial Infections; Cephalosporins; Diabetes Complications; Di

2017
Analysis of patients with diabetes and complicated intra-abdominal infection or complicated urinary tract infection in phase 3 trials of ceftolozane/tazobactam.
    BMC infectious diseases, 2017, 05-02, Volume: 17, Issue:1

    Topics: Adult; Aged; Anti-Bacterial Agents; Bacterial Infections; Cephalosporins; Diabetes Complications; Di

2017
Analysis of patients with diabetes and complicated intra-abdominal infection or complicated urinary tract infection in phase 3 trials of ceftolozane/tazobactam.
    BMC infectious diseases, 2017, 05-02, Volume: 17, Issue:1

    Topics: Adult; Aged; Anti-Bacterial Agents; Bacterial Infections; Cephalosporins; Diabetes Complications; Di

2017
Analysis of patients with diabetes and complicated intra-abdominal infection or complicated urinary tract infection in phase 3 trials of ceftolozane/tazobactam.
    BMC infectious diseases, 2017, 05-02, Volume: 17, Issue:1

    Topics: Adult; Aged; Anti-Bacterial Agents; Bacterial Infections; Cephalosporins; Diabetes Complications; Di

2017

Other Studies

5 other studies available for metronidazole and Necrotizing Pyelonephritis

ArticleYear
Emphysematous pyelonephritis in the setting of diabetes mellitus.
    The Journal of the Association of Physicians of India, 2011, Volume: 59

    Topics: Anti-Infective Agents; Diabetes Mellitus, Type 2; Diagnosis, Differential; Emphysema; Escherichia co

2011
Hydronephrosis and loin pain as a presentation of tubo-ovarian abscess developing after Mirena coil removal.
    BMJ case reports, 2012, Aug-02, Volume: 2012

    Topics: Abdominal Pain; Abscess; Adult; Anti-Infective Agents; Appendicitis; Device Removal; Diagnosis, Diff

2012
THERAPEUTIC PROBLEMS IN URINARY INFECTIONS.
    Southern medical journal, 1964, Volume: 57

    Topics: Chloramphenicol; Enterobacter aerogenes; Escherichia coli Infections; Humans; Hydrocortisone; Imidaz

1964
[Intra- and peri-renal gas formation. Bilateral emphysematous pyelonephritis].
    Der Urologe. Ausg. A, 1999, Volume: 38, Issue:3

    Topics: Aged; Combined Modality Therapy; Fatal Outcome; Female; Humans; Imipenem; Kidney; Lumbar Vertebrae;

1999
Treatment with metronidazole of three patients with serious infections due to Bacteroides fragilis.
    The Journal of antimicrobial chemotherapy, 1975, Volume: 1, Issue:2

    Topics: Adolescent; Bacteroides fragilis; Bacteroides Infections; Brain Abscess; Female; Humans; Kidney Fail

1975