Respiratory Tract Infections Clinical Trial
— STOP-ABOfficial title:
Safety of Discontinuing Patient Antibiotic Treatment When Physicians no Longer Consider it Necessary
NCT number | NCT02900820 |
Other study ID # | 16/101 |
Secondary ID | |
Status | Completed |
Phase | N/A |
First received | |
Last updated | |
Start date | January 2017 |
Est. completion date | December 2020 |
Verified date | October 2020 |
Source | Spanish Society of Family and Community Medicine |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
There is no evidence that discontinuing antibiotic therapy for non-bacterial infections is safe. The main objective of this study is to determine whether discontinuation of antibiotic therapy when a clinician no longer considers it necessary makes any difference in terms of the number of days with severe symptoms. This is a multicentre, open-label, randomised controlled clinical trial. The study will be conducted in ten primary care centres in Spain. We will include patients from 18 to 75 years of age with uncomplicated acute respiratory tract infections (RTIs) in whom: antibiotics are not necessary; or those diagnosed with clinical conditions for which antibiotics might be necessary but according to the history and clinical examination the physician considers that antibiotics are not needed or the patient feels that the antibiotic regimen has not worked as expected; or several doses of an antibiotic have been taken from leftovers found in the household or obtained at the pharmacy without any medical prescription for a clinical condition for which antibiotics are not necessary. The patients will be randomly assigned to the usual strategy of continuing antibiotic treatment (usual intervention group) or discontinuing antibiotic therapy (novel intervention group). A sample size of 215 patients per group was calculated on the basis of a reduction of one day in the duration of severe symptoms as a clinically relevant outcome. The primary outcome will be duration of severe symptoms, i.e. symptoms scored 5 or 6 by means of a symptom diary. Secondary outcomes will include: antibiotics taken, adverse events, patient satisfaction, and complications within the first 3 months.
Status | Completed |
Enrollment | 430 |
Est. completion date | December 2020 |
Est. primary completion date | June 2020 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years to 75 Years |
Eligibility | Inclusion Criteria: Patients with uncomplicated respiratory tract infections [common cold, influenza, pharyngitis, rhinosinusitis, acute bronchitis, and acute exacerbations of mild-to-moderate chronic obstructive pulmonary disease] who has previously taken any dose of antibiotic due to any of the following 3 clinical scenarios and accepts to participate in the clinical trial will be included: - Patients diagnosed with clinical conditions for which antibiotics are not necessary; - Patients diagnosed with a clinical condition for which antibiotics might be necessary but according to the history and clinical examination the primary health physician considers that antibiotics are not needed to be taken or the patients feel that the antibiotic regimen has not worked as expected and feel they need clinical reassessment - Patients who have taken some doses of an antibiotic (from leftovers found in the household or obtained at the pharmacy without any medical prescription) for a clinical condition for which antibiotics are not necessary Exclusion Criteria: - Subjects under 18 and over 75 years of age - Patients with confirmed bacterial infection - Patients requiring hospital admission - Severe impairment of signs (impairment of consciousness, respiratory rate > 30 respirations per minute, heart rate > 125 beats per minute, systolic blood pressure < 90 mm Hg, diastolic blood pressure < 60 mm Hg, temperature > 40°C, oxygen saturation < 92%) - Problems to comply with treatment at home - sociopathy or psychiatric problems, drug or alcohol addiction, or within an inadequate family setting - - Lack of tolerance to oral treatment, such as the presence of nausea and vomiting, gastrectomy, post-surgery and/or diarrhoea - Significant comorbidity, including severe renal failure, hepatic cirrhosis, severe heart failure, immunosuppression - chronic HIV infection, transplantation, neutropenic, or patients receiving immunosuppressive drugs or corticosteroids - - Terminal disease - Admitted to a long-term residence - Difficulty to attend the programmed visits - Refusal to participate in the study |
Country | Name | City | State |
---|---|---|---|
Spain | Guinardó Primary Care Center | Barcelona | Catalonia |
Spain | La Marina Primary Care Center | Barcelona | Catalonia |
Spain | Manso - Via Roma Primary Care Center | Barcelona | Catalonia |
Spain | Coll d'en Rabassa Primary Health Center | Palma de Mallorca | Balearic Islands |
Spain | Jaume I Primary Care Center | Tarragona | Catalonia |
Lead Sponsor | Collaborator |
---|---|
Spanish Society of Family and Community Medicine |
Spain,
Costelloe C, Metcalfe C, Lovering A, Mant D, Hay AD. Effect of antibiotic prescribing in primary care on antimicrobial resistance in individual patients: systematic review and meta-analysis. BMJ. 2010 May 18;340:c2096. doi: 10.1136/bmj.c2096. Review. — View Citation
Dekker AR, Verheij TJ, van der Velden AW. Inappropriate antibiotic prescription for respiratory tract indications: most prominent in adult patients. Fam Pract. 2015 Aug;32(4):401-7. doi: 10.1093/fampra/cmv019. Epub 2015 Apr 24. — View Citation
Gilbert GL. Knowing when to stop antibiotic therapy. Med J Aust. 2015 Feb 16;202(3):121-2. — View Citation
Goossens H, Ferech M, Vander Stichele R, Elseviers M; ESAC Project Group. Outpatient antibiotic use in Europe and association with resistance: a cross-national database study. Lancet. 2005 Feb 12-18;365(9459):579-87. — View Citation
Morgan DJ, Okeke IN, Laxminarayan R, Perencevich EN, Weisenberg S. Non-prescription antimicrobial use worldwide: a systematic review. Lancet Infect Dis. 2011 Sep;11(9):692-701. doi: 10.1016/S1473-3099(11)70054-8. Epub 2011 Jun 12. Review. — View Citation
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Duration of severe symptoms | Days with symptoms scoring 5 or 6 by means of a six-point Likert scale | From 14 to 28 days after the index visit | |
Secondary | Adverse effects of the medication | Any adverse effect appearing from day 0 to 28 | From index visit to 28 days after the initial visit | |
Secondary | Antibiotic consumption | Any antibiotic taken by the patient | From index visit to day 28 | |
Secondary | Satisfaction with health care by means of a questionnaire | Satisfaction degree stated by the patient at day 28 | Day 28 after the index visit | |
Secondary | Belief in the effectiveness of antibiotic therapy by means of a questionnaire | Degree of patient's belief in how effective antibiotics are for uncomplicated respiratory tract infections | Day 28 after the index visit | |
Secondary | Rate of complications | Any complication related to the uncomplicated respiratory tract infection within the 3 first months after the index visit | Within the first 3 months |
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