RAHM Foundation Retrospective Study of Various Diseases

NCT ID: NCT02359786

Last Updated: 2015-02-10

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

UNKNOWN

Total Enrollment

10000 participants

Study Classification

OBSERVATIONAL

Study Start Date

2011-01-31

Study Completion Date

2016-12-31

Brief Summary

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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.

Detailed Description

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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.

Conditions

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

Study Design

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Study Time Perspective

RETROSPECTIVE

Study Groups

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Genetic Testing Subjects undergoing genetic testing

No interventions assigned to this group

Topicals Subjects using topical compounds

No interventions assigned to this group

Patients undergoing Spinal Surgery using IOM

No interventions assigned to this group

Spine Patients undergoing cervical or lumbar surgery

No interventions assigned to this group

Total Joint Patients undergoing knee and hip replacement

No interventions assigned to this group

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

No interventions assigned to this group

Eligibility Criteria

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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
Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Rahm Foundation

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Other Identifiers

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RAHM 1002 v.6

Identifier Type: -

Identifier Source: org_study_id

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