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No medical product or device was administered to study patients, nor did participation in the study necessitate any change from standard of care.
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All medications were administered once daily in the morning via the Breezhaler® (Novartis Pharma AG, Stein, Switzerland) device except for tiotropium, which was administered via the HandiHaler® (Boehringer Ingelheim, Ingelheim, Germany) device.
Additionally, it is thought that the low use of Locators (5.2%) is strongly influenced by Japan's strict pharmaceutical regulations and because the MHLW in Japan had not yet licensed the device at the time the questionnaire was administered.
No medical product or device in addition to standard care was administered to study patients, nor did participation in the study necessitate any change from standard of care.
The first anesthesia was administered by simple devices consisting of glass or metal containers for sponges soaked in ether and allowed no control of dosage.
Forty-eight hours after P4 device removal, 10 μg of buserelin acetate was administered.
DermAll-OVA was administered topically with DermaPrep device to target Langerhans cells.
For general anesthesia, heated inhaled isoflurane was administered with an anesthesia device dedicated to small animals (Minerve, France).
Finally, an electronic version of the Beck Depression Inventory was administered on the handheld device.
ECT was administered by Thymatron DGX device (Somatics, ILC, lake Bluff, USA) through bilateral technique following a dose titration method.
In addition, the SF-12 Health Survey was administered using the same devices [ 23- 25].
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