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NCT Number: NCT07202234

Bacteriophage Cocktail Therapy for Multidrug-Resistant Gram-Negative Ventilator-Associated Pneumonia

The purpose of this study is to systematically evaluate the efficacy and safety of bacteriophage cocktail therapy in patients with ventilator-associated pneumonia caused by Gram-negative bacterial infections.

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Key information

About this study

This study investigates the clinical application of bacteriophage therapy in severe infections through a prospective, randomized, multi-center trial targeting ventilator-associated pneumonia (VAP) caused by multidrug-resistant Gram-negative bacteria. The trial will comprehensively assess the efficacy, safety, and applicability of inhaled bacteriophage cocktail therapy, providing high-quality clinical evidence to support the establishment of an evidence-based framework for phage therapy. The primary endpoint is clinical response rate, with secondary endpoints including bacterial clearance and 28-day mortality, aiming to determine the therapeutic potential and clinical value of phage cocktails in VAP treatment.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Diagnosed with ventilator-associated pneumonia (VAP);
  • Identified infection with MDR Klebsiella pneumoniae, Acinetobacter baumannii, or Pseudomonas aeruginosa via MROSE evaluation and antimicrobial susceptibility testing (AST) from this or other tertiary hospitals;
  • Aged 18 to 85 years;
  • Written informed consent obtained from the patient or legal guardian.

Exclusion criteria

  • Pregnant or breastfeeding women;
  • FiO₂ ≥ 70% or PEEP ≥ 15 cmH₂O;
  • Hemodynamic instability (vasopressor dose increased by ≥30% in the last 6 hours or norepinephrine > 0.5 μg/kg/min);
  • Known allergy to phage components.

Treatment and study plan

Phage cocktail administered via nebulization

Drug

Phage cocktail administered via nebulization,BID

Nebulized normal saline inhalation therapy

Drug

Nebulized normal saline inhalation therapy, BID

Primary outcomes

  1. Clinical response rate

    Time frame: From enrollment to the end of treatment (within 10 days of enrollment)

Secondary outcomes

  1. Bacterial clearance rate

    Time frame: 10 days after enrollment

  2. 28-day mortality

    Time frame: 28 days after enrollment

  3. Length of hospital stay

    Time frame: 28 days after enrollment

  4. Length of invasive mechanical ventilation

    Time frame: 28 days after enrollment

  5. CPIS score

    Time frame: 1,5,10 days after enrollment

    Full Title: Clinical Pulmonary Infection Score (CPIS);Range: Minimum: 0, Maximum: 12

    ;Interpretation: Higher score indicates more severe infection.

  6. SOFA score

    Time frame: 1,5,10 days after enrollment

    Full Title: Sequential Organ Failure Assessment (SOFA) Score;Range: Minimum: 0, Maximum: 24

    ;Interpretation: Higher score indicates greater organ dysfunction.

Study contacts

Contact information is provided by the study sponsor or research team.

Weihua Zhang

CONTACT

[email protected]

+86 18610607819

Xiuli Wang

CONTACT

[email protected]

+86 18686045253

Sponsors and collaborators

Lead sponsor

Chinese PLA General Hospital

Other

Collaborators

  • Chinese the Eighth Medical Center of the General Hospital of the People's Liberation Army
  • Henan Provincial People's Hospital
  • Peking University Third Hospital
  • The First Affiliated Hospital of Zhengzhou University
  • The First Medical Center of Chinese PLA General Hospital
  • Zhengzhou Central Hospital

Registry information

Official study title

A Randomized Controlled Trial of Bacteriophage Cocktail Therapy for Multidrug-Resistant Gram-Negative Ventilator-Associated Pneumonia

Important dates

Study start
2025
Primary completion
2028
Study completion
2028
First posted
Oct 1, 2025
Registry last updated
Oct 1, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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