- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT00512382
The Nature of Reflux-respiratory Symptoms Association in Difficult to Treat Wheezing\Coughing Babies
September 4, 2011 updated by: Avigdor Mandelberg, Wolfson Medical Center
The Nature of Reflux-respiratory Symptoms Association in Difficult to Treat Asthmatic/Wheezing Babies Using Impedance and Wheezy Monitoring
GER and respiratory symptoms are both common phenomenon in children.
Both can coexist in the same patient by chance alone.
Research reveals increased incidence for both to coexist leading to suspect a temporal association and possible causality.
Therefore we conducted an observational study To determine the primary cause (RS or GER)using for the first time both PH-Impedance as measurements of GER and Wheezy monitoring (WEEM) that records simultaneously wheeze and cough noises.
Both modalities will be recorded for 12-24 hours.
If GER precedes cough/wheeze recordings it points to GER being the possible precipitating factor and vice versa.
Study Overview
Status
Completed
Intervention / Treatment
Detailed Description
GER and respiratory symptoms are both common phenomenon in children.
Both can coexist in the same patient by chance alone.
Research reveals increased incidence for both to coexist leading to suspect a temporal association and possible causality.
Therefore we conducted an observational study To determine the primary cause (RS or GER)using for the first time both PH-Impedance as measurements of GER and Wheezy monitoring (WEEM) that records simultaneously wheeze and cough noises.
Both modalities will be recorded for 12-24 hours.
If GER precedes cough/wheeze recordings it points to GER being the possible precipitating factor.However, If cough/wheeze precedes GER recordings it points to cough/wheeze being the possible precipitating factor.
The recordings will be investigated 1 minute before and one minute after each event.
Study Type
Observational
Enrollment (Actual)
15
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
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Holon, Israel
- Wolfson Medical center and Sackler School of Medicine, Tel Aviv University, Tel
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-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
1 month to 1 year (Child)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Probability Sample
Study Population
We studied 23 consecutive Difficult to treat infants and children suspected of suffering from both RS and GER with chronic respiratory symptoms.
However, four dropted due to technical problems wiht the equipment.
In 19 patients We fully analyzed the respiratory sounds one minute during and one minute before and one minute after each GER episode, and in all parental markings of cough.
Description
Inclusion Criteria:
- Children 1 month - 18 years old
- Difficult to treat asthma
- Difficult to treat cough
- Difficult to treat other respiratory symptoms
Exclusion Criteria:
- Children on artificial ventilation
- Children not compliant with PH-Metria and/or WEEM
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Observational Models: Case-Only
- Time Perspectives: Prospective
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
A
Babies and small children 1-24 months
|
loudspeaker recording (WEEM) is attached externally to the chest simultaneously with PH-Impedance.
|
|
B
Children 2-18 years old
|
loudspeaker recording (WEEM) is attached externally to the chest simultaneously with PH-Impedance.
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Study Director: Avigdor Mandelberg, MD, Edith Wolfson Medical Center, and Sackler School of Medicine, Tel Aviv University, Tel aviv
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
March 1, 2007
Primary Completion (Actual)
March 1, 2011
Study Completion (Actual)
September 1, 2011
Study Registration Dates
First Submitted
August 6, 2007
First Submitted That Met QC Criteria
August 6, 2007
First Posted (Estimate)
August 7, 2007
Study Record Updates
Last Update Posted (Estimate)
September 7, 2011
Last Update Submitted That Met QC Criteria
September 4, 2011
Last Verified
September 1, 2011
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 688 special
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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