Hemodialysis. N18.5
Conditions
Interventions
Sponsors
Eligibility
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
| Measure | Time frame |
|---|---|
| Pruritus score. Timepoint: before intervention;8 weeks after intervention;20 weeks after intervention. Method of measurement: 5-D questionnaire. | — |
Secondary
| Measure | Time 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
Arak University of Medical Science