Chronic Obstructive Pulmonary Disease (COPD). Clinical Trial
Official title:
A Phase III Single-blind, Randomised Placebo Controlled Trial of Long Term Therapy in Patients With Stable COPD Using Moxifloxacin, Azithromycin and Doxycycline: a Bayesian Decision Analysis, Including Other Criteria, Will be Used to Distinguish the Optimal Antibiotic Treatment
Chronic Obstructive Pulmonary Disease (COPD) is the cause of considerable deaths, and exacerbations (flare up of symptoms) are a major cause of hospital admission in the UK. Bacterial infections play an important role in the development of COPD, however, there is little information available about the use of long term antibiotics in the treatment of this disease. Therefore the purpose of this study is to identify the best antibiotic regime for treating patients with COPD who have persistent bacterial infection in their lung. We will test a variety of approaches including both older and newer regimes prescribed either on a daily basis at a lower dose or in "pulsed" courses (for example, every other day or five days every month). The three antibiotics tested in this study are: moxifloxacin, azithromycin and doxycycline. This is a 13 weeks study conducted at the Royal Free Hospital, London. It is expected that approximately 200 patients will be selected for this study. The information we get from this study may help us to treat future patients with COPD better.
This is a 14 week study in which 200 patients with COPD will be selected for this study from
GP practices up to a 15 mile radius from the Royal Free Hospital to participate in this
study. The 3 antibiotic regimes (plus a placebo group) will be used in this study are:
Moxifloxacin: an oral dose of 400 mg once daily for 5 consecutive days every 4 weeks.
Azithromycin: an oral dose of 250 mg once daily three times a week (every other day).
Doxycycline: an oral dose of 100 mg once daily.
Placebo will be given as one table once daily.
Study recruitment and enrollment will take place through the Primary Care Research Network
(PCRN). Potentially eligible participants aged ≥ 45 will be identified from GP practices up
to a 15 mile radius from the RFH. Potential eligible patients will be contacted by letter
with an accompanying patient information sheet (PIS) describing the study in detail and
inviting the patient to attend a hospital visit and enroll. If patients have not responded
to the invitation letter, this will be followed by a reminder letter approximately 2 weeks
later. Non responders to the reminder letter will be followed up by a final telephone call.
Patients expressing an interest in participation will be offered a screening appointment at
the Royal Free Hospital. Patients will be asked to visit the hospital 3 times and will be
contacted twice by telephone during the course of the study.
At the Screening Visit (V1), the following will take place:
- The study will be discussed again with the patient during this visit and if he/she
agree to participate, they will be asked to sign the consent form.
- A medical history of the patient will be taken. This will include smoking history,
antibiotic Hypersensitivity, as well as patient concomitant medication.
- A full physical examination will be performed and height and weight of patients will be
recorded.
- A lung function test (spirometry assessment) will be performed.
- A blood sample will be collected in order to perform routine haematology/blood
chemistry and liver function.
- A sputum sample will be taken and analysed to determine number of bacteria in the lung
and to screen for Tuberculosis.
- A urine pregnancy test will be carried out on females of childbearing potential.
- Patients will be asked to complete two sets of questionnaires; "St. George's
respiratory questionnaire" (SGRQ) which includes simple questions about the patients
COPD condition and how it affects their life; the second an EQ5D questionnaire which
includes simple questions relating to the general quality of their life.
- Patients will be given daily diary cards and asked to record their symptoms.
- An ECG will be performed on all patients.
If patients are eligible for the trial, they will be randomised to one of the following
groups:
Moxifloxacin: an oral dose of 400 mg once daily for 5 consecutive days every 4 weeks for a
total duration of 13 weeks.
Azithromycin: an oral dose of 250 mg once daily three times a week (every other day) for a
total duration of 13 weeks.
Doxycycline: an oral dose of 100 mg once daily, for a total duration of 13 weeks Placebo: an
oral daily dose of one capsule, for a total duration of 13 weeks.
This is a single-blind trial. Patients will be blinded to treatment; the investigator will
be unblinded. Microbiologists will also be blind to treatment allocation when assessing
sputum samples.
Following randomisation of eligible patients, patients will be asked to return to the
hospital for a second visit (within 1 week) to collect their medication from the research
fellow who will instruct the patient to start taking the medication within 3 days. At this
visit, the research team will check if patients are happy filling in their diary cards and
will be happy to answer any questions they may have.
In week 5 and week 9 of treatment, each patient will be contacted by telephone to:
- Monitor progress and compliance.
- Remind patients to take medication.
- Encourage patients to contact the GP/investigator if symptoms worsen.
- The occurrence of any adverse effects/serious adverse effects (AE/SAE) or an
exacerbation will be checked and recorded.
- Remind patients to fill in their daily diary cards
End of Study Visit (at week 14):
Patients will be asked to return to the hospital and the following assessments will be made:
- The occurrence of AE/SAE or exacerbations will be checked and recorded.
- A spirometry assessment to test their lung function.
- Diary cards will be collected by the investigator.
- SGRQ and EQ5D questionnaires will be completed at this visit by the patient.
- A sputum sample will be taken from the patients to determine bacterial number in their
lung.
- Unused study medication and packaging will be collected from the patient.
;
Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Single Blind (Subject)
| Status | Clinical Trial | Phase | |
|---|---|---|---|
| Completed |
NCT01962935 -
Study to Investigate Safety, Tolerability and Effect of Multiple Dosing With AZD 4721 and/or With AZD 5069
|
Phase 1 |