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Investigation of antipruritic effect of oral nicotinamide in uremic patients

Investigation of antipruritic effect of oral nicotinamide in uremic patients

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT201202068940N1
Enrollment
50
Registered
2012-04-13
Start date
2011-06-22
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

Uremic pruritus. Symptoms, signs and abnormal clinical and laboratory findings, not elsewhere classified

Interventions

Intervention 1: placebo. Intervention 2: oral nicotinamide 500 mg two times a day.
Placebo
Treatment - Drugs
placebo
oral nicotinamide 500 mg two times a day

Sponsors

Jundishapur University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: known cases of end-stage renal disease patients treated with hemodialysis; ages between 18 and 60 years; At least 6 weeks history of pruritus; no systemic or topical treatment for the pruritus. Exclusion criteria: a known hypersensitivity to nicotinamide; suffering from other known skin diseases, liver disorders, metabolic disorders, any other condition except for CRD causing pruritus; any serious systemic disease; Usage of antihistamines or other anti-pruritus drugs in the last three months.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Attenuation of uremic pruritus. Timepoint: Four weeks. Method of measurement: By using a traditional Visual Analogue Scale (VAS) and a modified questionnaire method (pruritus score).

Countries

Iran (Islamic Republic of)

Contacts

Public ContactAhmad Khazanee

Jundishapur University of Medical Sciences

khazani.a@ajums.ac.ir , dr_khazani@yahoo.com+98 61 1222 4344

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026