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Effect of fluvoxamine in pruritus in hemodialysis patients

Effect of fluvoxamine in pruritus in hemodialysis patients

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2012111211438N1
Enrollment
53
Registered
2012-11-25
Start date
2012-07-22
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

Hemodialysis. N18.5

Interventions

Intervention 1: The 53 hemodialysis patients that are having inclusion criteria are screened with questionnaire. They are randomly divided in two groups( drug and placebo) Treatment in the drug group
Treatment - Drugs
Placebo
The 53 hemodialysis patients that are having inclusion criteria are screened with questionnaire. They are randomly divided in two groups( drug and placebo) Treatment in the drug group is started wit
treatment in the placebo group is started with dose of 50mg placebo (one tablet) daily at night and added every 5-7 days 25 mg until reaches to maximum 200mg (with patient tolerance). Then it given wi
Treatment in the drug group is started with dose of 50mg of fluvoxamine (one tablet) daily at night and added every five to seven days 25mg, until reaches to maximum dose 200mg (with patient tolerance

Sponsors

Arak University of Medical Science
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 70 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria;hemodialysis patients; filling the testimonial questionnaire;age 20-70 years;thrice weekly hemodialysis;KT/V>0.9(keeping the optimum adequecy of dialysis) exclusion criteria:dermatitis disease;B and C hepatitis;cholestasis and other liver disease;treatment with corticosteroid in recent months;anemia(Hb<10);treatment with other SSRI;TCA;MAOI;5-HT3 receptor antagonist ;phenothiazine;lithium;history of seizure;pregnancy and breastfeeding;hypomania;consumption of theophylinand warfarin;sever chronic nausea;hyponatremia

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Pruritus score. Timepoint: before intervention;8 weeks after intervention;20 weeks after intervention. Method of measurement: 5-D questionnaire.

Secondary

MeasureTime frame
Fluvoxamine. Timepoint: weekly. Method of measurement: milligram.;Placebo. Timepoint: weekly. Method of measurement: milligram.;Side effects. Timepoint: weekly. Method of measurement: quallitative.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr.zohreh sadat nikjoo

Arak University of Medical Science

Z.S.nikjoo@gmail.com+98 861417360212

Outcome results

None listed

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