Blind clinical trial device

Surgery – Means for introducing or removing material from body for... – Treating material introduced into or removed from body...

Reexamination Certificate

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C604S403000, C604S257000, C206S438000

Reexamination Certificate

active

06544250

ABSTRACT:

TECHNICAL FIELD OF THE INVENTION
The invention relates to a device for blinding the administration of nonsolid pharmaceutical presentations in clinical trials on mammals.
PRIOR ART
In the prior art there are various known ways of blinding the administration of nonsolid presentations in clinical trials. If the pharmaceutical presentation is a colorless liquid, then the pharmaceutical presentation can be replaced for example by a physiological saline solution. In the case of colored presentations, an opaque application system, for example, can be used for administration. It is obvious that these methods are not suitable for intrapulmonary administration. In the case of clinical testing of nonsolid presentations which are administered by the intrapulmonary route, the double-blind technique is therefore used. [J. A. Schwarz (1995), Leitfaden Klinische Prüfungen: Planung, Organisation, Durchführung, Dokumentation und Überwachung (Guidelines for Clinical Trials: Planning, Organization, Conduct, Documentation and Monitoring), ECV-Editio Cantor-Verlag; Der pharmazeutische Betrieb; Vol. 43; or M. S. Kwong et al., Double-Blind Clinical Trial of Calf Lung Surfactant Extract for the Prevention of Hyaline Membrane Disease in Extremely Premature Infants; Pediatrics (1985), Vol. 76, No. 4, pages 585-592]. Here, the test substance is administered by persons who are not otherwise involved with the patient during the clinical study. These persons are then under a pledge of secrecy. The double-blind technique can only be carried out with considerable outlay in terms of personnel and costs.
SUBJECT OF THE INVENTION
It is an object of the present invention to make available a device for blinding the administration of nonsolid pharmaceutical presentations in clinical trials in a simple manner and without using the double-blind technique.
The subject of the invention is therefore a device for blinding the administration of nonsolid pharmaceutical presentations in clinical trials on mammals.
In one aspect of the invention, the device is an opaque container which has at least two attachments, one of which is intended for connection to.a dispenser for the pharmaceutical presentation, and the other of which is intended for connection to an applicator, and where the inside of the container has means for holding back the pharmaceutical presentation (hereinafter also referred to as the nonflow-type configuration).
When such a container is connected to a dispenser and to an opaque applicator for administration of a pharmaceutical presentation, said pharmaceutical presentation is held back in the container upon application, but this cannot be detected by the person charged with the administration.
In a further aspect, the invention concerns an opaque container which has at least two attachments, one of which is intended for connection to a dispenser for the pharmaceutical presentation, and the other of which is intended for connection to an applicator, and where the attachments in the inside of the container have a continuous connection which ensures that the pharmaceutical presentation is transported through the container (hereinafter also referred to as the flow-type configuration).
If this container is used together with a dispenser and an opaque applicator to administer the pharmaceutical presentation, said pharmaceutical presentation is transported through the container and administered to the patient, but this cannot be detected by the person charged with the administration.
In a further aspect, the invention relates to a container with which it is possible both to transport the pharmaceutical presentation through the container and also to hold back the pharmaceutical presentation in the same container. A further subject of the invention is therefore an opaque container which has at least three attachments, two of which are intended for connection to a dispenser for the pharmaceutical presentation, and the third one of which is intended for connection to an applicator, and where the inside of the container has means for holding back the pharmaceutical presentation, and one of the attachments which are intended for connection to a dispenser has a continuous connection to the attachment which is intended for connection to the applicator, and the connection ensures that the pharmaceutical presentation is transported through the container.
Depending on the choice of attachments for connection to the dispenser and the applicator, the pharmaceutical presentation is either transported through the container and administered to the patient or is held back in the container.
The container according to the invention can be rigid or flexible and can be made from all suitable solid materials. The container is advantageously one which has been made using plastic or rubber (e.g. film bag made of PVC film).
The means for holding back the pharmaceutical presentation inside the container is preferably an absorbent material which is not able to completely take up the nonsolid pharmaceutical presentation (e.g. absorbent fabric). However, the container can also be completely or partially hollow on its inside. The pharmaceutical presentation can also be held back in this way. Depending on the nature of the means for holding back the pharmaceutical presentation (hereinafter also referred to as the test substance), the container is preferably dimensioned such that it can completely accommodate the test substance to be administered. In a preferred embodiment of the invention, the container is dimensioned such that it can accommodate 300 ml of liquid. Containers are preferred which have an internal volume of 500 ml to 3000 ml, and particularly preferred are those which have an internal volume of 1000 ml to 2000 ml.
Depending on the weight and the quantity of the test substance to be administered, the container should preferably have a correspondingly greater own weight. This makes it difficult or even impossible for the person administering the substance to compare the weight of the container before and after administration of the test substance. Containers with an own weight of more than 1 kg have generally proven advantageous in this respect. In a preferred embodiment of the invention, the inside of the container can have weight elements in order to ensure an adequate own weight of the container. The weight elements can for example be hard rubber disks.
The attachments which the container according to the invention possesses are preferably commercially available Luer lock attachments which are suitable for connection to the dispenser and applicator. The attachments preferably have different markings for purposes of differentiation. The dispenser is preferably a commercially available syringe which can be connected to the attachment on the container directly or via a tube connection. The applicator is preferably an opaque applicator, for example an opaque catheter system, preferably a catheter system which is suitable for intrapulmonary administration of a nonsolid pharmaceutical presentation. Such catheters are known to those versed in the art.
The container according to the invention which holds back the pharmaceutical presentation can, at the attachment intended for connection to the dispenser, also be connected to a tube which leads into the inside of the container and has an open end through which the pharmaceutical presentation is dispensed into the inside of the container. The tube advantageously has a plurality of openings in the tube line. This ensures rapid dispensing of the pharmaceutical presentation into the inside of the container. The tube can also advantageously have a nonreturn valve which ensures that the pharmaceutical presentation dispensed into the inside of the container cannot return into the tube. The attachment intended for connection to the applicator can have a closure inside the container, so that the pharmaceutical presentation held back cannot escape into the applicator. If so desired, this can entail a closed tube guided through the inside of the container. In a preferred embodiment of

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