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Status unknownNCT01618175Updated Jun 13, 2012

Home Oxygen Treatment of Childhood Acute Bronchiolitis

An interventional study of Home oxygen therapy in Bronchiolitis, Viral and Home Nursing, sponsored by Soroka University Medical Center. Status unknown. Open to participants aged 2 Months to 24 Months. Per ClinicalTrials.gov, last updated 2012-06-13.

Sponsored by Soroka University Medical Center · Not applicable, Interventional, and Treatment

The sponsor has not verified this record recently (last verified May 2012), so the status shown — last known as Not yet recruiting — may be out of date.
Phase
Not applicable
Study type
Interventional
Enrollment
85
Allocation
Not applicable
Ages
2 Months to 24 Months
Sex
All
01

Study summary

Background: acute bronchiolitis (AB) is a common reason for hospitalization of infants in all population groups, and is usually due to respiratory syncytial virus (RSV) infection. The main cause for hospitalization is often a need for oxygen, but can also include high fever (with a suspected secondary bacterial infection) or increasing respiratory distress. In a minority of cases (some of which can be identified in advance by defining risk groups) a serious illness may develop, including risk of respiratory failure and death. Most cases will just require supplemental oxygen and suction of secretions from the nose (as listed in the recommendations of the American Academy of Pediatrics - AAP). However, this apparently "simple" treatment still requires continued hospitalization. This results in a sharp increase in bed occupancy in Israeli hospital pediatric departments in the winter months. In recent years two studies from developed countries have been published where safety has been demonstrated for home oxygen treatment for babies with AB. However, feasibility studies have not been published yet, for example for populations living in poor conditions. The General Health Services (Klalit) in Israel provides integrated hospital and community health service to the majority of the population living o in our region, thus presenting an opportunity for optimal interventions related to this disease.

Read the detailed description

Objective: To develop a model of community based safe handling of AB in various communities in southern Israel.

Methods: A prospective intervention study examining the safety and health expenditures in infants with AB treated first in hospital but then discharged earlier with home oxygen while monitored in the community.

Contribution to the focus areas, and the impact of results on health policy planning: 1) Reducing hospitalization days and general financial savings. 2) Ability to implement these findings to populations with variable socio-economic backgrounds. 3) Prevention of nosocomial infections related morbidity.

Innovation and uniqueness in the study: test of this hypothesis precisely in our region, where populations have different socio-economic backgrounds, will build a model that may be suitable for all levels of society.

02

Conditions studied

  • Bronchiolitis, Viral
  • Home Nursing

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Keywords

  • Bronchiolitis, Viral
  • Home oxygen therapy
  • Home Nursing
  • Outcome and Process Assessment (Health Care)
  • bronchiolitis severity score
03

In context

Bronchiolitis, Viral

30 studies on the registry are indexed under Bronchiolitis, Viral; 2 are open to participants now.

This study's planned enrollment of 85 is close to the median of 85 across 25 interventional studies indexed under Bronchiolitis, Viral.

Browse Bronchiolitis, Viral studies →

Lead sponsor

Soroka University Medical Center is the lead sponsor of 160 studies on the registry; 2 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
2 Months to 24 Months
Sexes eligible
All
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  1. Age: 2-24 months, but age postconception of over 44 weeks.
  2. Ac. bronchiolitis clinical diagnosis: acute respiratory illness including nasal congestion, coughing and wheezing or crackles simplified, Tachypnea or retractions of the chest.
  3. X-ray confirms a viral diagnosis of bronchiolitis
  4. First attack of wheezing
  5. O2 Saturation \< 91% room air while arrival to the ER
  6. The baby and his family have a way to return to the ER after discharge
  7. The family lives a distance of less than 30 minutes drive from the center of Emergency Medicine
  8. The baby lives in an environment with no smoking
  9. The baby's family is available by phone
  10. The baby's family is ready for continuous monitoring of the baby at home 11th. Disease severity index (RDSS) of \< 4 (see definitions)

Exclusion criteria

Exclusion Criteria:

  1. Previous morbidity: cardiac, pulmonary, neuromuscular, nutrition (including FTT). And congenital or acquired airway problem.
  2. Age since conception is less than -44 weeks.
  3. History of apneas
  4. Bacterial pneumonia suggested by a localized-focal finding on X-ray
  5. Previous wheezing attack
  6. O2 Saturation > 92% on room air
  7. Family has no transportation available follow-up visits
  8. The family lives at a distance greater than 30 minutes drive from the medical facility
  9. The baby was treated with for this attack
  10. There is no continuous monitoring of the baby at home
Terms in these criteria, in plain language(1)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

Corticosteroids (steroids)

Anti-inflammatory medicines such as prednisone, prednisolone and dexamethasone — not the anabolic steroids used for muscle.

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05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
85 participants (estimated)

Study arms

  • Experimental
    Home oxygen therapy

    Infants with acute bronchiolitis of low to moderate severity will be discharged home with supplemental oxygen and monitored by phone calls and home visits.

    Device: Home oxygen therapy

Interventions

  • DeviceHome oxygen therapy

    Oxygen will be provided using a generator, through nasal prongs at a flow rate up to 1 L/min. During home stay the parents will be guided on how to suspect signs of clinical deterioration. General treatment: If oxygen saturation by pulse oximeter is greater than 92%, the oxygen will be reduced by a quarter liter per minute while monitoring for 15 minutes. If oxygen saturation decreased to less than 92% of the child will remain with the best previous oxygen flow until the next visit. Once the child reaches - 0.06 l / min for 15 minutes, he will will be checked back on room air. Cessation of oxygen therapy: when the oxygen saturation remains above 92% on room air. Every day that no home visit was performed a phone call will be done and follow-up questionnaire will be filled daily, including oxygen saturation registration.

06

What researchers measure

Primary outcomes

  1. Rate of hospital readmission within 10 days after discharge with home oxygen

    Readmission to the hospital because of (1) increased oxygen requirement (\> 1 L\\ minute through the nose) to maintain oxygen saturation of\> 92%. (2) event of apnea. 3) feeding of less than 50% of normal with clinical evidence of dehydration, (4) the parents or pediatrician wish remove the child from the study.

    Time frame: Within 10 days from discharge home with O2

07

Study locations

No study locations are listed for this record.

08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jun 13, 2012, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT01618175
Responsible party
Sponsor
First posted
Jun 13, 2012
Start date
Oct 2012
Primary completion
Jun 2013 (estimated)
Completion
Aug 2014 (estimated)
Last update
Jun 13, 2012
View the source record on ClinicalTrials.gov ↗

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This study is status unknown, as verified in May 2012. You cannot join it, but the record below documents what was studied.

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