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Effect of N-Acetylcysteine in hemodialysis patients

Effect of N-Acetylcystein on serum Malondialdehyde in comparison with placebo in chronic hemodialysis patients

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
IRCT
Registry ID
IRCT2014031216969N1
Enrollment
60
Registered
2014-07-31
Start date
2014-04-21
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

Condition 1: Hemodialysis patients. Condition 2: Hemodialysis patients. Condition 3: Hemodialysis patients. Renal failure Renal failure Renal failure

Interventions

Treatment - Drugs
Placebo
Intervention 1: Intervention group: N-acetylcysteine with the trade name Fluimucil, as 600 milligram tablet, made by Swiss Zambon Svizzerasa company, given twice daily (every 12 hours), per oral for 6
Intervention group: N-acetylcysteine with the trade name Fluimucil, as 600 milligram tablet, made by Swiss Zambon Svizzerasa company, given twice daily (every 12 hours), per oral for 6 weeks.
Control group: Placebo as 600 milligram tablet, twice daily, every 12 hours, per oral for 6 weeks, made from micro-crystalline cellulose, lactose, corn starch, talk (2% of total tablet weight) which m

Sponsors

Vice Chancellor for Development, Research and Technology of Ahvaz Jondishapour University of Medical
Lead Sponsor

Eligibility

Sex/Gender
All
Age
16 Years to 100 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: 1) all of the chronic hemodialysis patients due to end stage renal disease more than 18 years old and at least three months has been past from starting of hemodialysis. Exclusion criteria: 1) Every acute disease leads to hospitalization from one month before trial. 2) Allergy to N-acetylcysteine. 3) Hepatic cirrhosis 4) Using Vitamin E or C or every known antioxidant from two weeks before intervention. 5) congestive heart failure or ejection fraction less than 35%. 6) Non using of N-acetylcysteine or placebo more than 20% of total drug.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Serum Malondialdehyde. Timepoint: Before intervention and 6 weeks after intervention. Method of measurement: With malondialdehyde kit spectrophotometry method in mmol/lit.

Secondary

MeasureTime frame
Itching. Timepoint: Before intervention and 6 weeks after intervention. Method of measurement: Visual.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactAli Javaherforoushzadeh

Ahvaz Jondishapour University of Medical Sciences

Ali_javaherforoush@yahoo.com; Javaherforoushzadeh.a@ajums.ac.ir+98 61 1374 3013

Outcome results

None listed

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