IVRCC’s electronic system to execute a placebo response reduction strategy was used in one recent phase II study evaluating subjects with Major Depressive Disorder (MDD). Sequential Parallel Comparison Design (SPCD) is just one example of a recent randomization design innovation for which IVRCC’s custom programmed systems were utilized to achieve a faster, smaller, lower cost trial with statistically better data.
IVRCC's custom-built native app was an ideal choice for the Operating Room that had no access to Wi-Fi, by being able to accommodate a large number of Inclusion/Exclusion criteria, the possibility of tablet or internet failure, and proper randomization treatment assignment exactly per protocol.
The client compared the costs of our BYOD system with two other bids which collected data from subjects using proprietary handheld devices. With our IVR system, patients use their own phone or smartphone for daily diary collection, which saved the client several hundred thousand dollars.
IVRCC collaborated with the client on a multi-center, randomized, double-blind, parallel group, vehicle-controlled study. The client realized a significant cost savings by combining two protocols, IRT application build, validation, hosting and maintenance costs into one application.
From project managers to administrators and programmers, the IVRCC team worked closely with the client to design and create custom applications that tracked and displayed the results of diary compliance to the participants. All calculations were in real-time so that the system reporting was current and accessible at all times.
IVRCC was able to provide an affordable and adaptable solution that provided data that was easy to integrate with the final EDC database. The study article was recently published in The New England Journal of Medicine.
Find out how our automated supply management resulted in less work and better inventory control. The objective of this study was to evaluate the safety, tolerability and efficacy on subjects with opioid-induced constipation. Clinical trial materials management services provided by IVR Clinical Concepts were a key component to the success of this study. Patients were provided kits which included medication and a Bristol Stool Scale.
The technical storage or access is strictly necessary for the legitimate purpose of enabling the use of a specific service explicitly requested by the subscriber or user, or for the sole purpose of carrying out the transmission of a communication over an electronic communications network.
The technical storage or access is necessary for the legitimate purpose of storing preferences that are not requested by the subscriber or user.
The technical storage or access that is used exclusively for statistical purposes.The technical storage or access that is used exclusively for anonymous statistical purposes. Without a subpoena, voluntary compliance on the part of your Internet Service Provider, or additional records from a third party, information stored or retrieved for this purpose alone cannot usually be used to identify you.
The technical storage or access is required to create user profiles to send advertising, or to track the user on a website or across several websites for similar marketing purposes.