Schwartzstein 1987.
Methods | Double‐blind, randomised, cross‐over trial | |
Participants | 12 patients (male = 8, female = 4) with chronic stable asthma Mean age 28 years (22 to 44) Mean duration of asthma 16 years (3 to 30) |
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Interventions |
Treatments administered in identical capsules |
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Outcomes | FEV1 and FVC collected at: 0, 15, 30, 45, 60, 75, 90, 105, 120, 150, 180, 210, 240 minutes
If FEV1 declined ≥ 10%, FEV1 and FVC were also measured at 270, 300, 330, 360 minutes Symptoms: 24, 48 hours |
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Notes | Diagnostic criteria: American Thoracic Society This study was supported in part by the International Glutamate Technical Committee |
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Risk of bias | ||
Bias | Authors' judgement | Support for judgement |
Random sequence generation (selection bias) | Unclear risk | "The order in which the test substances were given was randomly assigned" Comment: Not described |
Allocation concealment (selection bias) | Unclear risk | Not described |
Blinding (performance bias and detection bias) All outcomes | Low risk | "both subjects and investigators were blinded as to the identity of the medications being given." The drugs were administered in identical capsules |
Incomplete outcome data (attrition bias) All outcomes | Low risk | Results of all the subjects were reported |
Selective reporting (reporting bias) | Low risk | All the results described in method chapter were reported |
Other bias | Unclear risk | "This study was supported in part by the International Glutamate Technical Committee" Comment: we are not certain whether it would influence the result |