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Clinical Trial for the Assessment of Delayed Antibiotic Treatment in Pediatric (DAP-Pediatrics) (DAP)

Primary Purpose

Rhinosinusitis, Acute Bronchitis, Acute Otitis Media

Status
Completed
Phase
Phase 4
Locations
Spain
Study Type
Interventional
Intervention
Antibiotic prescription strategies
Sponsored by
Asociacion Colaboracion Cochrane Iberoamericana
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Rhinosinusitis focused on measuring Delayed antibiotic treatment, Acute respiratory infections, Pediatrics, Satisfaction

Eligibility Criteria

2 Years - 14 Years (Child)All SexesDoes not accept healthy volunteers

General Inclusion Criteria:

In this study can be enrolled children (2 to 14 ages) with non-complicated acute respiratory tract infections, including pharyngotonsillitis, rhinosinusitis, acute bronchitis and acute media otitis. The doctors include children with these infections if they have reasonable doubts if they should treat with antibiotics.

General Exclusion Criteria:

  • Patients not aged between 2 and 14.
  • Patients have participated in the DAP-pediatrics previously.
  • Patients are severely affected or patients has been felt severely affected for one week (all time).
  • Patients with symptoms and signs suggestive of serious illness or severely affected and/or complications (particularly pneumonia, mastoiditis, peritonsillar abscess, peritonsillar cellulitis, intraorbital or intracranial complications).
  • Patients at high risk of serious complications due to prior comorbidity. This includes significant heart disease, lung, kidney, liver or neuromuscular, immunosuppression, cystic fibrosis.

Sites / Locations

  • Asociación Colaboración Cochrane Iberoamericana

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Active Comparator

No Intervention

Experimental

Arm Label

Direct antibiotic treatment

No antibiotic treatment

Delayed antibiotic prescription

Arm Description

The doctor gives to parents an antibiotic prescription for their son's respiratory infection which he should start immediately.

The doctor does not give to parents an antibiotic prescription for their son's respiratory infection.

The doctor gives to parents an antibiotic prescription for their son's respiratory infection with the advice to use it if needed, in case of worsening of symptoms or not improve.

Outcomes

Primary Outcome Measures

Duration and severity of symptoms
Coordination Centre performed telephone interviews.

Secondary Outcome Measures

Antibiotic consumption
Self-reported by the patients and checked at the Regional Pharmacy's Units.
Parents satisfaction with treatment
Likert scale.
Parents' belief in the efficacy of antibiotics
Likert scale
Impact of DAP strategy on the reconsultation
Medical history review
The prescription of antibiotics in the previous two years predicts the effect of prescribing strategies in reconsultation.
Medical history review

Full Information

First Posted
February 26, 2013
Last Updated
July 27, 2017
Sponsor
Asociacion Colaboracion Cochrane Iberoamericana
Collaborators
Instituto de Salud Carlos III, Ministry of Health, Spain
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1. Study Identification

Unique Protocol Identification Number
NCT01800747
Brief Title
Clinical Trial for the Assessment of Delayed Antibiotic Treatment in Pediatric (DAP-Pediatrics)
Acronym
DAP
Official Title
Clinical Trial for the Assessment of Delayed Antibiotic Treatment in the Non-complicated Acute Respiratory Tract Infections in Pediatric (Study DAP-Pediatrics)
Study Type
Interventional

2. Study Status

Record Verification Date
July 2017
Overall Recruitment Status
Completed
Study Start Date
June 2012 (Actual)
Primary Completion Date
June 7, 2016 (Actual)
Study Completion Date
June 7, 2016 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Asociacion Colaboracion Cochrane Iberoamericana
Collaborators
Instituto de Salud Carlos III, Ministry of Health, Spain

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The general hypothesis is that delayed antibiotic treatment strategy present similar effectiveness, when compared with non-prescription of antibiotics or the prescription of antibiotics, in the non-complicated acute respiratory tract infections in pediatric patients.
Detailed Description
The current project (DAP Pediatrics) is a study that explores the optimization of antibiotic prescribing in our country by evaluating the delayed prescription of antibiotics. The proposed trial will take place in the context of a prior similar study we conducted in adults. The study currently underway is the DAP-Adults study (a randomised controlled trial that evaluates several antibiotic prescribing strategies, including de delayed prescription in uncomplicated acute respiratory infections in adults in primary care). The aim of this study DAP-Pediatrics (randomized, multicenter parallel) to determine the efficacy and safety of delayed prescription of antibiotics compared to direct prescription and non-prescription of antibiotic in uncomplicated acute respiratory infections in pediatric patients. This 3 arms clinical trial will include 450 children and will evaluate the duration and severity of symptoms, antibiotic consumption, parents' satisfaction, the perceived efficacy of antibiotics and the number of visits generated. The project also includes a qualitative study, by means of structured interviews, to assess the perception and attitudes of parents towards the different treatment strategies and carry out a full analysis of economic evaluation.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Rhinosinusitis, Acute Bronchitis, Acute Otitis Media, Pharyngotonsillitis
Keywords
Delayed antibiotic treatment, Acute respiratory infections, Pediatrics, Satisfaction

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Model Description
Antibiotic treatment versus delayed antibiotic treatment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
450 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Direct antibiotic treatment
Arm Type
Active Comparator
Arm Description
The doctor gives to parents an antibiotic prescription for their son's respiratory infection which he should start immediately.
Arm Title
No antibiotic treatment
Arm Type
No Intervention
Arm Description
The doctor does not give to parents an antibiotic prescription for their son's respiratory infection.
Arm Title
Delayed antibiotic prescription
Arm Type
Experimental
Arm Description
The doctor gives to parents an antibiotic prescription for their son's respiratory infection with the advice to use it if needed, in case of worsening of symptoms or not improve.
Intervention Type
Other
Intervention Name(s)
Antibiotic prescription strategies
Intervention Description
The patients enrolled will be randomized between three treatment strategies or arms. Patients randomized to delayed treatment arm or direct treatment, doctors can choose the antibiotic that they consider appropriate depending on such local resistance or practice.
Primary Outcome Measure Information:
Title
Duration and severity of symptoms
Description
Coordination Centre performed telephone interviews.
Time Frame
30 days
Secondary Outcome Measure Information:
Title
Antibiotic consumption
Description
Self-reported by the patients and checked at the Regional Pharmacy's Units.
Time Frame
30 days
Title
Parents satisfaction with treatment
Description
Likert scale.
Time Frame
30 days
Title
Parents' belief in the efficacy of antibiotics
Description
Likert scale
Time Frame
30 days
Title
Impact of DAP strategy on the reconsultation
Description
Medical history review
Time Frame
1 year
Title
The prescription of antibiotics in the previous two years predicts the effect of prescribing strategies in reconsultation.
Description
Medical history review
Time Frame
1 year
Other Pre-specified Outcome Measures:
Title
Complications of disease
Description
Included by doctors or coordination centre
Time Frame
30 days

10. Eligibility

Sex
All
Minimum Age & Unit of Time
2 Years
Maximum Age & Unit of Time
14 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
General Inclusion Criteria: In this study can be enrolled children (2 to 14 ages) with non-complicated acute respiratory tract infections, including pharyngotonsillitis, rhinosinusitis, acute bronchitis and acute media otitis. The doctors include children with these infections if they have reasonable doubts if they should treat with antibiotics. General Exclusion Criteria: Patients not aged between 2 and 14. Patients have participated in the DAP-pediatrics previously. Patients are severely affected or patients has been felt severely affected for one week (all time). Patients with symptoms and signs suggestive of serious illness or severely affected and/or complications (particularly pneumonia, mastoiditis, peritonsillar abscess, peritonsillar cellulitis, intraorbital or intracranial complications). Patients at high risk of serious complications due to prior comorbidity. This includes significant heart disease, lung, kidney, liver or neuromuscular, immunosuppression, cystic fibrosis.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Pablo Alonso Coello, PhD
Organizational Affiliation
Asociación Colaboración Cochrane Iberoamericana
Official's Role
Principal Investigator
Facility Information:
Facility Name
Asociación Colaboración Cochrane Iberoamericana
City
Barcelona
ZIP/Postal Code
08041
Country
Spain

12. IPD Sharing Statement

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Clinical Trial for the Assessment of Delayed Antibiotic Treatment in Pediatric (DAP-Pediatrics)

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