Abstract | BACKGROUND: OBJECTIVES: SEARCH STRATEGY: We searched the Cochrane Cystic Fibrosis and Genetic Disorders Group trials register which comprises references identified from comprehensive electronic database searches, handsearching relevant journals and abstract books of conference proceedings. Additional searches were carried out on MEDLINE (1966 to 2002) and EMBASE (1981 to 2002).Date of the most recent search of the Group's haemoglobinopathies register: May 2002. SELECTION CRITERIA: Randomised or quasi-randomised controlled trials. Trials using quasi-randomisation methods will be included in future updates of this review if there is sufficient evidence that the treatment and control groups are similar at baseline. DATA COLLECTION AND ANALYSIS: MAIN RESULTS: REVIEWER'S CONCLUSIONS:
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Authors | J A Knight-Madden, I R Hambleton |
Journal | The Cochrane database of systematic reviews
(Cochrane Database Syst Rev)
Issue 3
Pg. CD003733
( 2003)
ISSN: 1469-493X [Electronic] England |
PMID | 12917983
(Publication Type: Journal Article, Review, Systematic Review)
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Chemical References |
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Topics |
- Acute Disease
- Anemia, Sickle Cell
(complications)
- Bronchodilator Agents
(administration & dosage)
- Chest Pain
(drug therapy, etiology)
- Cough
(drug therapy, etiology)
- Dyspnea
(drug therapy, etiology)
- Fever
(drug therapy, etiology)
- Humans
- Nebulizers and Vaporizers
- Syndrome
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