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Diable Medical
  Volunteer Today
Home     Current Studies     Study Participants     Sponsors & CROs     About Us     Contact Us
Do you have Diabetes
and suffer with
Diabetic Neuropathy?
Volunteer for a study
Clinical Study:
Diabetic Peripheral Neuropathy
Volunteer Today
Study: Dong-A DAI3011
Status: Enrolling
In/Outpatient: Outpatient
This is a double-blind, randomized, parallel group, dose ranging
, placebo-controlled study where eligible subjects (age 18 to 75
years) will have an average pain score ≥ 4 on an 11-point Liker
t numerical rating scale (NRS) for at least four days each week prior
to randomization as assessed by daily pain diaries. Eligible subjects
will be randomized to a 1:1:1:1 ratio to receive 300mg, 600mg,
900mg of DA-9801, or placebo three times a day for 12 weeks.
During and at the end of the 12-week treatment period subjects will
be evaluated for safety and efficacy parameters. A follow-up visit for
safety will occur four weeks after the last treatment visit (TV).
Physicians Note
The purpose of this study is to determine whether DA-9801 is
effective in the treatment of pain associated with diabetic
Qualifications - Inclusions & Exclusions:
Inclusion Criteria:
• Must be 18 to 75 years of age
• Diagnosed with Type I or Type II diabetes
• HbA1c ≤ 12% at the time of screening
Diablo Clinical Research
2255 Ygnacio Valley Road, Suite M
Walnut Creek, CA 94598
Compensation for Time
and Travel:
Our patient volunteers receive all labs,
physical exams, specialty exams
(mammograms, bone density tests,
x-rays, etc) and specialty consults
(dietitian, ophthalmologist, etc) free of
charge. No insurance is required.
Volunteers are paid for their time and
travel. LEARN MORE >>
• Has diabetic neuropathic pain (numbness, soreness, shooting or poking pain) in the legs for more than three
  months prior to screening and with no adequate relief from other treatments
• Has an average pain score of ≥ 4 for 24 hours at least four days out of the week prior to randomization as
  assessed by the 11-point Likert NRS
• If female of childbearing potential, subject must have a negative serum pregnancy test at screening
• Understands and is willing to participate in the clinical study and can comply with study procedures and visits.
• Normal cognitive and communicative ability as judged by clinical assessment and ability to complete
  self-reported questionnaires
• Subject is willing and able to give informed consent
Learn More Volunteer Today  
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