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Efficacy and safety of pregabalin for the treatment of neuropathic pain in patients undergoing hemodialysis

Efficacy and safety of pregabalin for the treatment of neuropathic pain in patients undergoing hemodialysis - Efficacy and safety of pregabalin in patients undergoing hemodialysis

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000023117
Enrollment
30
Registered
2016-07-11
Start date
2015-03-01
Completion date
Unknown
Last updated
2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

neuropathic pain

Interventions

An initial dose of pregabalin at 25 mg
this was then increased up to a maximum of 150 mg.

Sponsors

Nihon University School of Medicine Divisions of Nephrology, Hypertension and Endocrinology, Department of Internal Medicine
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Hemodialysis duration > 6 months at enrollment. Patients who could make a decision. Patients who were diagnosed with peripheral neuropathic pain by a neurologist.

Exclusion criteria

Exclusion criteria: (1) age < 20 years or > 85 years, (2) a history of severe heart failure, angina, myocardial infarction, or stroke within the past 6 months, (3) the presence of infectious disease, thyroid disease, malignant tumors, or treatment with steroids or immunosuppressants, (4) current hospitalization, (5) patients with a history of angioedema, and (6) patients with dementia who experience difficulty making a decision

Design outcomes

Primary

MeasureTime frame
VAS(baseline and 12 weeks)

Secondary

MeasureTime frame
SF-8,HS-CRP(baseline and 12 weeks) Blood cell counts, levels of serum creatinine, serum urea nitrogen, total protein, albumin, electrolytes, total cholesterol, low-density lipoprotein cholesterol, triglyceride, serum iron, total iron binding capacity, serum ferritin, high-sensitivity C-reactive protein, serum beta-2-microglobulin, intact parathyroid hormone Kt/V systolic and diastolic blood pressure, heart rate, cardiothoracic ratio adverse events

Countries

Japan

Contacts

Public ContactTomoyasu Otsuki

Nihon University School of Medicine Divisions of Nephrology, Hypertension and Endocrinology, Department of Internal Medicine

totsuki16@gmail.com0339728111

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026