Trial record 10 of 2442 for:    Open Studies | "Anti-Bacterial Agents"

CRP-guided Antibiotic Treatment in COPD Exacerbations Admitted to the Hospital (CATCH)

The recruitment status of this study is unknown because the information has not been verified recently.
Verified March 2012 by Medical Center Alkmaar.
Recruitment status was  Recruiting
Sponsor:
Information provided by (Responsible Party):
W.G.Boersma, Medical Center Alkmaar
ClinicalTrials.gov Identifier:
NCT01232140
First received: November 1, 2010
Last updated: March 21, 2012
Last verified: March 2012
  Purpose

Rationale: Acute exacerbations are key events in chronic obstructive pulmonary disease (COPD), resulting in poorer quality of life. Causes include irritants, viruses and bacterial pathogens. These exacerbations are often treated with a combination of corticosteroids, bronchodilators and antibiotics, but the benefit of antibiotic therapy remains controversial. Several trials studying antibiotic treatment in AECOPD showed conflicting data, with several large studies failing to demonstrate superiority of antibiotic therapy over placebo. Other trials indicated that antibiotic therapy is effective in patients who have at least two of the following symptoms: increased dyspnoea, increased sputum volume and increased sputum purulence. Ever since sputum purulence has been used as a predictive marker in AECOPD, a strategy that has been integrated in the GOLD guideline for treatment of AECOPD. However, the color of sputum reported by patients is not always reliable and inspection of sputum is not always possible. Several serum biomarkers such as C-reactive protein (CRP) and procalcitonin (PCT) are now available. In a recent trial of doxycycline in addition to systemic corticosteroids for patients hospitalized with AECOPD we found that CRP might be valuable as a marker predictive of response to antibiotic treatment in AECOPD.


Condition Intervention
COPD
Exacerbation
Bronchitis
Sputum
C-Reactive Protein
Other: CRP-guided antibiotic treatment

Study Type: Interventional
Study Design: Allocation: Randomized
Endpoint Classification: Efficacy Study
Intervention Model: Parallel Assignment
Masking: Open Label
Primary Purpose: Treatment
Official Title: CRP-guided Antibiotic Treatment in Patients Hospitalized With Acute Exacerbations of COPD Patients. A Randomized Controlled Intervention Trial.

Resource links provided by NLM:


Further study details as provided by Medical Center Alkmaar:

Primary Outcome Measures:
  • Number of patients treated with antibiotics during hospital stay [ Time Frame: 10 days ] [ Designated as safety issue: No ]
    Sputum purulence has been used as a predictive marker in AECOPD.However, the color of sputum reported by patients is not always reliable and inspection of sputum is not always possible. Serum biomarker such as C-reactive protein (CRP) represents systemic inflammation.In the present study, we will compare CRP guided antibiotic treatment versus treatment according to GOLD strategy. Our hyposthesis is that CRP-guided therapy results in lower number of antibiotic prescriptions


Secondary Outcome Measures:
  • Time to treatment failure within 30-days [ Time Frame: 30 days ] [ Designated as safety issue: No ]
    Treatment failure within 30 days after hospital admission will be compared

  • Length of stay [ Time Frame: 30 days ] [ Designated as safety issue: No ]
    Length of hospital stay for the exacerbation

  • Time to next exacerbation [ Time Frame: 1 year ] [ Designated as safety issue: No ]
    Time to the next exacerbation with a follow-up period of one year

  • Symptom scores (VAS-LRTI, George's Respiratory Questionnaire) [ Time Frame: 30 days ] [ Designated as safety issue: No ]
    Symptom score (VAS-LRTI) and Quality of life (George's Respiratory Questionnaire) will be measured at onset and recovery.

  • Adverse events [ Time Frame: 30 days ] [ Designated as safety issue: Yes ]
    Adverse events of antibiotic treatment are recorded during follow-up


Estimated Enrollment: 220
Study Start Date: July 2011
Estimated Study Completion Date: July 2013
Estimated Primary Completion Date: March 2013 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
Experimental: CRP-guided antibiotic treatment
If CRP> 50 mg/l a patient receive antibiotic treatment, whereas in those patients with CRP =< 50 mg/l antibiotic treatment is withheld.
Other: CRP-guided antibiotic treatment
If CRP> 50 mg/l patients with AECOPD receive antibiotic treatment, whereas in those patients with CRP =< 50 mg/l antibiotic treatment are withheld. This will be compared to the regular antibiotic treatment that has been advised by the GOLD strategy
GOLD strategy-antibiotic treatment
According to the GOLD strategy a patient with an AECOPD should prescribed antibiotic treatment if a patient has symptoms of increased dyspnea, increased sputum production and change of sputum color. Two of these three criteria should be present, however change in sputum production is obligatory.
Other: CRP-guided antibiotic treatment
If CRP> 50 mg/l patients with AECOPD receive antibiotic treatment, whereas in those patients with CRP =< 50 mg/l antibiotic treatment are withheld. This will be compared to the regular antibiotic treatment that has been advised by the GOLD strategy

Detailed Description:

Objective: CRP-guided antibiotic therapy will be compared with standard antibiotic therapy in AECOPD. Our aim is that CRP guided therapy will lead to 20% reduction in antibiotic consumption.

Study design: randomized controlled intervention trial Study population: Hospitalised COPD patients with acute exacerbation. Intervention (if applicable): Patients with type 1 and 2 exacerbation will be assigned to either CRP guided therapy or antibiotic therapy according to GOLD guidelines.

Main study parameters/endpoints: The main endpoint of the study is the reduction in antibiotic consumption. Furthermore, the real incidence of infiltrates in AECOPD with fever will be studied. As secondary outcome the objectives length of hospitalization, time to treatment failure within 30-days and time to next exacerbation will be assessed. The relation between the level of biomarkers the presence of infiltrates on the HRCT will be investigated.

Subjective improvement in symptoms will be measured by symptoms (VAS-LRTI) and quality of life will be assessed by St George's Respiratory Questionnaire. Finally, adverse effects of the antibiotic treatment will be recorded.

In order to observe a significant difference of antibiotic consumption, 60% in standard antibiotic group and 40% in CRP guided antibiotic group, with a power of 0.8, a total of 110 patients have to be assigned by randomisation to each group.

Nature and extent of the burden and risks associated with participation, benefit and group relatedness: Patients in both treatment arms will receive a non-experimental treatment. Both treatment options are recognized as part of standard care. The burden associated with participation is limited to a total of 3 visits to the hospital and phone call for data assessment at regular follow-up. There are no specific risks involved in participating. Less adverse effects may be beneficially for the patient.

  Eligibility

Ages Eligible for Study:   40 Years and older
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • Age 40 or over. No upper age limit will be employed.
  • Written informed consent obtained.
  • AECOPD according to the GOLD guideline. An exacerbation of COPD is defined as an event in the natural course of the disease characterized by a change in the patient's baseline dyspnoea, cough, and/or sputum that is beyond normal day-to-day variations, is acute in onset, and may warrant a change in regular medication in a patient with underlying COPD.
  • Criteria for hospital admission according to the GOLD: marked increase in symptoms (i.e. resting dyspnoea), severe underlying COPD, onset of new physical signs (cyanosis, edema), failure to respond to initial medical management, significant co morbidities, frequent exacerbations, newly occurring arrhythmias, diagnostic uncertainty.
  • Former of current smoker with a minimum smoking history of 10 pack years.
  • Patients have to be capable of ingesting oral medication.
  • Patients have to be mentally capable of participating in the study (able to complete questionnaires and perform lung function tests).
  • Life expectancy ≥ 30 days.

Exclusion Criteria:

  • Pregnant or lactating women, or women of childbearing age not using an acceptable method of contraception.
  • Pretreatment with corticosteroids (cumulative dose >210 mg) for the present exacerbation.
  • Progression or new radiographic abnormalities on the chest X-ray or CT scan compatible with pneumonia.
  • bronchiectasis (HRCT confirmed).
  • Cystic fibrosis.
  • Tuberculosis.
  • Immunodeficiency disorders such as AIDS, humoral immune defect, ciliary dysfunction etc., and the use of immunosuppressive drugs (>30 mg prednisolone/day maintenance dose or equivalent for more than 4 weeks).
  • Recent or unresolved lung malignancy.
  • Other disease likely to require antibiotic therapy, such as recurrent sinusitis or urinary tract infection.
  • Significant gastrointestinal or other conditions that may affect study drug absorption.
  • Class III or IV congestive heart failure or stroke.
  • Newly diagnosed pulmonary embolism
  Contacts and Locations
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its ClinicalTrials.gov identifier: NCT01232140

Locations
Netherlands
W.G.Boersma Recruiting
Alkmaar, Noord-Holland, Netherlands, 1829JC
Contact: W.G. Boersma, PHD,MD    0031-725482750    w.boersma@mca.nl   
Contact: J.M.A. Daniels, PHD, MD    0031204444444    j.daniels@vumc.nl   
Principal Investigator: W.G. Boersma, PHD, MD         
Principal Investigator: J.M.A. Daniels, PHD,MD         
Sub-Investigator: C.S. de Graaff, MD         
Sponsors and Collaborators
Medical Center Alkmaar
Investigators
Study Director: W.G. Boersma, PHD,MD Medical Centre Alkmaar
  More Information

Publications:
Responsible Party: W.G.Boersma, PhD, Medical Center Alkmaar
ClinicalTrials.gov Identifier: NCT01232140     History of Changes
Other Study ID Numbers: CATCH study, AECOPD
Study First Received: November 1, 2010
Last Updated: March 21, 2012
Health Authority: Netherlands: The Central Committee on Research Involving Human Subjects (CCMO)

Keywords provided by Medical Center Alkmaar:
COPD
exacerbation
antibiotic treatment
CRP
sputum
inflammation

Additional relevant MeSH terms:
Anti-Bacterial Agents
Antibiotics, Antitubercular
Bronchitis
Pulmonary Disease, Chronic Obstructive
Bronchial Diseases
Respiratory Tract Diseases
Lung Diseases, Obstructive
Lung Diseases
Respiratory Tract Infections
Anti-Infective Agents
Therapeutic Uses
Pharmacologic Actions
Antitubercular Agents

ClinicalTrials.gov processed this record on July 22, 2014