- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg NCT01008761
Trial for the Treatment of Acute Asthma in Wheezy Pre-school Aged Children
11. juli 2012 opdateret af: Janielee Williamson
A Double Blind Randomized Control Trail of Azithromycin for the Acute Management of Wheezy Pre-school Children
To determine if treatment of pre-school children with a history of wheeze who present to an Emergency Department with an acute wheezing episode with azithromycin for 5 days will resolve their symptoms more quickly, will require less short acting beta agonist (SABA), and allow these children to remain symptom free for a longer period of time.
Studieoversigt
Status
Ukendt
Betingelser
Intervention / Behandling
Undersøgelsestype
Interventionel
Tilmelding (Forventet)
440
Fase
- Ikke anvendelig
Kontakter og lokationer
Dette afsnit indeholder kontaktoplysninger for dem, der udfører undersøgelsen, og oplysninger om, hvor denne undersøgelse udføres.
Studiesteder
-
-
Alberta
-
Calgary, Alberta, Canada, T3B 6A8
- Rekruttering
- Alberta Children's Hospital
-
Ledende efterforsker:
- David Johnson, MD
-
Kontakt:
- Janielee Williamson, RN
- Telefonnummer: 403-955-3186
- E-mail: janie.williamson@albertahealthservices.ca
-
Kontakt:
- Paula Finnson
- Telefonnummer: 403-955-7873
- E-mail: paula.finnson@albertahealthservices.ca
-
Underforsker:
- Sheldon Spier, MD
-
Underforsker:
- James D Kellner, MD
-
Underforsker:
- Candice Bjornson, MD
-
Underforsker:
- Michael Surrette, PhD
-
Underforsker:
- Alberto Nettle-Aguire, PhD
-
Edmonton, Alberta, Canada, T6G 2V7
- Rekruttering
- Stollery Children's Hospital
-
Kontakt:
- Piush Mandhane, MD
- E-mail: piush.mandhane@albertahealthservices.ca
-
Ledende efterforsker:
- Piush Mandhane, MD
-
Underforsker:
- William Craig, MD
-
Underforsker:
- Darryl Adamko, MD
-
Underforsker:
- Bonita Lee, MD
-
Underforsker:
- Carina Majaesic, MD
-
-
Deltagelseskriterier
Forskere leder efter personer, der passer til en bestemt beskrivelse, kaldet berettigelseskriterier. Nogle eksempler på disse kriterier er en persons generelle helbredstilstand eller tidligere behandlinger.
Berettigelseskriterier
Aldre berettiget til at studere
1 år til 5 år (Barn)
Tager imod sunde frivillige
Ingen
Køn, der er berettiget til at studere
Alle
Beskrivelse
Inclusion Criteria:
- 12-60 months
- wheeze on auscultation
Exclusion Criteria:
- antibiotic use in the past 30 days
- macrolide allergy
- underlying medical condition
- significant co-morbidities
- current enrollment
- language barrier or no access to phone for follow up
Studieplan
Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
- Primært formål: Behandling
- Tildeling: Randomiseret
- Interventionel model: Parallel tildeling
- Maskning: Firedobbelt
Våben og indgreb
Deltagergruppe / Arm |
Intervention / Behandling |
|---|---|
|
Aktiv komparator: Zithromax, 100 mgmgs; 5mls suspension
Azithromycin given at 10 mg/kg/day for day 1, then 5 mg/kg for 4 days Each syringe will contain 12.5 mls (250 mgs) sufficient drug to adequately dose children who with up to 25 kgs (95%tile for weight for 60 month old child)
|
Azithromycin given at 10 mg/kg/day for day 1, then 5 mg/kg for 4 days Each syringe will contain 12.5 mls (250 mgs) sufficient drug to adequately dose children who with up to 25 kgs (95%tile for weight for 60 month old child)
Andre navne:
|
|
Placebo komparator: Suspension placebo,
placebo (suspension produced by CDC Edmonton.)
given at 10 mg/kg/day for day 1, then 5 mg/kg for 4 days.
|
Placebo suspension will be administered on day 1 at 10mg/kg and then for the next 4 days at 5 mg/kg
Andre navne:
|
Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Tidsramme |
|---|---|
|
To determine if treatment of pre-school children with a history of wheeze who present to an Emergency department (ED) with an acute wheezing episode with Azithromycin for 5 days will resolve their symptoms more quickly
Tidsramme: Patient is followed by phone day 1,3,5,7,14, with an in person return visit on day 21 and then by phone again every 2 weeks for 6 months
|
Patient is followed by phone day 1,3,5,7,14, with an in person return visit on day 21 and then by phone again every 2 weeks for 6 months
|
Sekundære resultatmål
Resultatmål |
Tidsramme |
|---|---|
|
Treatment of pre-school children with acute wheezing symptoms with 5 days of azithromycin will cause these children to use less rescue beta2 agonists than those treated with placebo
Tidsramme: Patient is followed by phone day 1,3,5,7,14, with an in person return visit on day 21 and then by phone again every 2 weeks for 6 months
|
Patient is followed by phone day 1,3,5,7,14, with an in person return visit on day 21 and then by phone again every 2 weeks for 6 months
|
|
Treatment of pre-school children with acute wheezing symptoms with 5 days of azithromycin will allow these children to remain free of subsequent wheezy episodes longer than those treated with placebo.
Tidsramme: Patient is followed by phone day 1,3,5,7,14, with an in person return visit on day 21 and then by phone again every 2 weeks for 6 months
|
Patient is followed by phone day 1,3,5,7,14, with an in person return visit on day 21 and then by phone again every 2 weeks for 6 months
|
Samarbejdspartnere og efterforskere
Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.
Sponsor
Samarbejdspartnere
Efterforskere
- Ledende efterforsker: David W Johnson, MD, Alberta Children's Hospital/University of Calgary
- Ledende efterforsker: Piush Mandhane, MD, Stollery Children's Hospital Edmonton
Datoer for undersøgelser
Disse datoer sporer fremskridtene for indsendelser af undersøgelsesrekord og resumeresultater til ClinicalTrials.gov. Studieregistreringer og rapporterede resultater gennemgås af National Library of Medicine (NLM) for at sikre, at de opfylder specifikke kvalitetskontrolstandarder, før de offentliggøres på den offentlige hjemmeside.
Studer store datoer
Studiestart
1. januar 2010
Primær færdiggørelse (Forventet)
1. december 2012
Studieafslutning (Forventet)
1. december 2013
Datoer for studieregistrering
Først indsendt
4. november 2009
Først indsendt, der opfyldte QC-kriterier
5. november 2009
Først opslået (Skøn)
6. november 2009
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Skøn)
12. juli 2012
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
11. juli 2012
Sidst verificeret
1. juli 2012
Mere information
Begreber relateret til denne undersøgelse
Nøgleord
Yderligere relevante MeSH-vilkår
Andre undersøgelses-id-numre
- ALAWhZy2010
Disse oplysninger blev hentet direkte fra webstedet clinicaltrials.gov uden ændringer. Hvis du har nogen anmodninger om at ændre, fjerne eller opdatere dine undersøgelsesoplysninger, bedes du kontakte register@clinicaltrials.gov. Så snart en ændring er implementeret på clinicaltrials.gov, vil denne også blive opdateret automatisk på vores hjemmeside .
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-
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-
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