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Serotonin-Norepinephrine Reuptake Inhibitor
Intervention for Peripheral Neuropathy
Phase 2
Waitlist Available
Research Sponsored by Southeastern Regional Medical Center
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 180 days
Awards & highlights
Study Summary
This study is evaluating whether a drug may help reduce pain for individuals who have chemotherapy.
Eligible Conditions
- Peripheral Neuropathy
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 180 days
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~180 days
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Assessment with respect to duloxetine of the effect of lorcaserin on the Pain Numerical Rating Scale.
Assessment with respect to duloxetine of the effect of lorcaserin on the patient-reported quality of life.
Trial Design
2Treatment groups
Experimental Treatment
Active Control
Group I: InterventionExperimental Treatment1 Intervention
Lorcaserin 10 mg bid
Group II: ControlActive Control1 Intervention
Duloxetine 60 mg qd
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Lorcaserin
FDA approved
Find a Location
Who is running the clinical trial?
Southeastern Regional Medical CenterLead Sponsor
1 Previous Clinical Trials
30 Total Patients Enrolled
Frequently Asked Questions
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