RAHM Foundation Retrospective Study of Various Diseases

Rahm Foundation

Status: Unknown

Conditions: Pain, Spinal Surgeries, Hip and Knee Joint Replacement, Adverse Events

Study type: Observational

Funder types: Other

Identifiers

NCT02359786

RAHM 1002 v.6

Details and patient eligibility

About

This is a retrospective data collection on treatment of various disorders. This registry will include a variety of different products, implants, technologies and procedures. The registry will also collect any adverse events/complications that occur during or following treatment of these conditions. The data may be utilized to develop strategic treatment pathways and/or benchmarking that will improve patient care. Ultimately, the goal of the registry is to enhance the understanding of healthcare and the treatment in these disease states.

Full description

The purpose is to collect data on patients with a variety of disorders. This includes point of care (primary care, internal medicine, pain management providers, etc.) as well as a variety of specialty providers including neurosurgeons, orthopedic surgeons, oncologists, and dermatologists. The retrospective data collection will consist of a core set of data if available. The registry will attempt to collect data prior to surgery/treatment/procedures, during surgery, and various time points following surgery/treatment/procedures. The data will include, but is not limited to demographic data, past medical history, previous treatments, time off of work, type of surgery performed, products/implants/procedures/technology used during surgery, treatments/procedures/technology used for non-surgical conditions, anesthesia used during surgery, complications/adverse events following surgery and or treatment, outcome tools, imaging results, pain assessment, pain medication utilization, length of hospital stay, unplanned hospital admissions, revision surgery, adjacent level disease, genetic testing, urinary drug testing, other diagnostic or assessment testing, patient return to work and patient return to normal activity. The data collected will vary depending on disease state and treatment. This registry will also allow for comparisons on different treatments, procedures, etc. with a goal of developing the best pathways for a variety of different disease states.

Enrollment: 10,000 estimated patients

Sex: All

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

• Subjects who meet eligibility criteria across 1 of the 6 therapeutic areas

Exclusion criteria

• Subjects who do not meet eligibility criteria for any of the 6 therapeutic areas

Trial design

10,000 participants in 6 patient groups

Genetic Testing Subjects undergoing genetic testing

Topicals Subjects using topical compounds

Patients undergoing Spinal Surgery using IOM

Spine Patients undergoing cervical or lumbar surgery

Total Joint Patients undergoing knee and hip replacement

UDT (unrinary drug test) Patients who are given a UDT