Case Studies

  • Case Study: Acute In-Hospital Study

    Rescue, First Patient in 18 months prior, Pivotal study Fewer than 10% of patients randomized of 186 required Publication Date Scheduled 9 months out Referral Chain unaware of study In-trial processes not being followed properly Mostly University Hospitals with local... Read more…

  • Case Study: Informed Consent

    Rheumatology, 1 ongoing study, 1 new parallel study Current consent rate at 7% and cost of randomized patient at $1,950 Very difficult I/E criteria Educated patient population Poly Pharmacy situation with many qualified candidates, requiring wash-out and discontinuation... Read more…

  • Case Study: Assistant Study Coordinator

    Cardiology study with very specific inclusion/exclusion criteria Large cardiology practices with large patient databases Too time consuming for regular study coordinator Varied EMR and paper records No EMR off-site review process available (no EMR consistency)... Read more…

  • Case Study: Integrated, Centralized Recruitment

    Depression/Anxiety combined study with 6 treatment arms 148 sites in US and Canada 1,600 patient randomization goal Varied SC experience levels Plan began at investigator meeting ICTS Solutions Recruitment roll-out at investigator meeting Study coordinator... Read more…

  • Case Study: Assistant Study Coordinator

    Therapeutic Area:  Ophthalmology Indication:  Dry AMD Needed 180 patients to complete device study that had begun more than 30 months prior After 30 months, sites were experiencing study fatigue and were underperforming ICTS identified 6 primary sites to assist... Read more…

  • Case Study: Special Populations

    (Hypertension) This was an NIH Phase IV program designed to enroll two, 10,000 subject groups within a five year period for a long term (10 year) study. ICTS designed and implemented a patient recruitment program covering 528 sites in the US, Canada, US Virgin Islands and Puerto Rico in six... Read more…

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