Center For Clinical Research
Pain Management
Why pick this one
Center For Clinical Research conducts chronic and acute pain trials in Winston-Salem and typically schedules screening within 24 hours of initial contact.
Best for
- Adults seeking participation in chronic pain clinical research
- People with chronic low back pain, migraine, neuropathy, fibromyalgia, osteoarthritis, or related pain conditions
- Participants able to attend scheduled visits at the Winston-Salem research facility
- Patients interested in investigational medications, devices, or treatment approaches
Look elsewhere if
- People seeking conventional pain treatment rather than clinical trial participation
- People seeking diagnosis or immediate treatment without a research screening process
- People unable to attend scheduled study visits in Winston-Salem
Specialties
- acute pain clinical studies
- chronic pain clinical studies
- chronic low back pain clinical studies
- chronic migraine pain clinical studies
- complex regional pain syndrome studies
- diabetic peripheral neuropathy studies
- fibromyalgia studies
- joint pain clinical studies
- neuropathy studies
- osteoarthritis studies
- post-herpetic neuralgia studies
- SI joint pain studies
- amputee pain studies
- cancer pain studies
- abdominal pain clinical studies
What makes them different
- Founded in January 2000
- Medical doctors with 30+ years of clinical research experience
- Principal investigators are key opinion leaders in chronic, acute, and neurologic pain
- Clinical research coordinators average 12+ years of tenure
- In-house recruitment team using multiple recruitment strategies
- Response time
- Screen visits are typically scheduled within 24 hours of initial contact
- Years in business
- 20+
- Serves
- Winston-Salem
Distilled from this business's own website.
Contact & Location
- Address
- 145 Kimel Park Dr Ste 330, Winston Salem, NC 27103-6972
- Phone
- 13367656181
- Website
- https://centerforclinicalresearch.com
Services
- clinical trial site management
- clinical trial participant recruitment and screening
- Phase I-IV clinical trials
- post-marketing studies
- real-world evidence studies
- regulatory management
- subject study visits onsite and remote
- drug and device accountability
- IRB submission and correspondence
- protocol feasibility
- study execution and closeout