Respiratory Respiratory
Conditions
Interventions
Single blind randomised controlled trial. The protocol compares histamine (to induce bronchoconstriction) with normal saline (as control) i.e. no bronchoconstriction.
Sponsors
Department of Health
Eligibility
Inclusion criteria
Inclusion criteria: Volunteers - 8, ages 18-75
Exclusion criteria
Exclusion criteria: Not provided at time of registration
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| 1. To determine if ventilation scintigraphy can be used to determine and quantify regional changes in ventilation in the lung following histamine challenge in normal subjects 2. Also to determine the extent to which these correlate with changes in overall lung function | — |
Secondary
| Measure | Time frame |
|---|---|
| Not provided at time of registration | — |
Countries
United Kingdom
Outcome results
None listed