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Brief Title: Prospective Evaluation of Intrathecal Targeted Drug Delivery for Cancer Associated Pain
Official Title: Intrathecal Targeted Drug Delivery for Cancer Associated Pain
Study ID: NCT05674240
Brief Summary: This Registry study will prospectively evaluate the differences in treatment outcomes in terms of pain intensity, pain interference, concomitant medication use, health-related quality of life, opioid adverse effects, and healthcare utilization between targeted drug delivery and conservative medication management only groups.
Detailed Description: This is a prospective, open-label, short term patient registry where up to 169 subjects with cancer associated pain will be enrolled. Subjects with cancer associated pain who are receiving conservative medical management (CMM) only and cancer patients receiving Intrathecal Drug Delivery system (IDDs) along with CMM will be followed for up to 3 months. Subjects will be evaluated monthly up to 3 months from the medical care initiation which is the implant day for the IDDs group and start of the new treatment plan for the CMM group. Subjects that decide to cross-over to the IDDs group in a future date, will still be followed for their progress. Based on routine care, subjects will be seen at day of implant, 1 month post-implant, 2 months post-implant, and 3 months post-implant.
Minimum Age: 21 Years
Eligible Ages: ADULT, OLDER_ADULT
Sex: ALL
Healthy Volunteers: No
Advocate Aurora Health, Oshkosh, Wisconsin, United States
Name: Mansoor M Aman, MD
Affiliation: Advocate Health Care
Role: PRINCIPAL_INVESTIGATOR