Clinical Trials Directory

Trials / Completed

CompletedNCT02460614

Effects of Rhinopharyngeal Retrograde Clearance in Children With Acute Viral Bronchiolitis

Comparison Between Rhinopharyngeal Retrograde Clearance and Nasopharyngeal Aspiration in Children With Acute Viral Bronchiolitis

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
100 (actual)
Sponsor
Pontificia Universidade Católica do Rio Grande do Sul · Academic / Other
Sex
All
Age
12 Months
Healthy volunteers
Not accepted

Summary

The purpose of this study is to compare the immediate effects of retrograde rhinopharyngeal clearance with nasopharyngeal aspiration in children admitted with acute viral bronchiolitis. The investigators selected children, up to 12 months old, admitted for acute viral bronchiolitis. Patients were divided in aspiration group (AG), submitted to nasopharyngeal aspiration, and clearance group (CG), submitted to retrograde rhinopharyngeal clearance with physiological solution (0.9%) instillation (RRC) technique. In both groups children were evaluated three times in the same day in order to verify cardiorespiratory parameters, clinical score of respiratory dysfunction and adverse effects.

Detailed description

Children up to 12 months old, admitted for acute viral acute viral bronchiolitis were selected. All children participating in the study should be in the first 48 hours of hospitalization. Patients were divided in aspiration group (AG), submitted to nasopharyngeal aspiration, and clearance group (CG), submitted to retrograde rhinopharyngeal clearance (RRC) technique with physiological solution (0.9%) instillation. In both groups children were evaluated three times in the same day (data collection 1 (C1) - performed early in the morning; data collecting 2 (C2) - performed in the early afternoon; and data collecting 3 (C3) - performed in the evening). In each data collection, cardiorespiratory parameters and clinical score of respiratory dysfunction were evaluated before procedures (T0), 10 minutes after (T1) and 30 minutes after (T2). Adverse effects were evaluated during the whole day of the study.

Conditions

Interventions

TypeNameDescription
PROCEDURERhinopharyngeal clearanceAt the end of the expiratory time, the child's mouth was closed by the hand of the researcher (raising the lower jaw), leading the child to perform a nasal aspiration maneuver.
PROCEDUREAspirationA sterile aspiration catheter was connected to an extension and carefully introduced into the nasal cavity of the patient.
OTHER0.9% saline0.9% saline consists of physiological solution and was instilled in both experimental groups.

Timeline

Start date
2013-03-01
Primary completion
2013-10-01
Completion
2013-12-01
First posted
2015-06-02
Last updated
2015-06-03

Source: ClinicalTrials.gov record NCT02460614. Inclusion in this directory is not an endorsement.