Skip to content

Effect of N -Acetylcysteine in treatment of hemodialysis patients

Effect of N - Acetylcysteine on hemoglobin and hematocrit in comparison with placebo in chronic hemodialysis patients

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
IRCT
Registry ID
IRCT2014051917757N1
Enrollment
78
Registered
2015-02-13
Start date
2015-01-10
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 patients. Renal failure

Interventions

Intervention 1: Intervention group: N - Acetylcysteine with trade name of mucomyst, as 600 milligram tablet, made by swiss zambon company, given twice daily (every 12 hours), per oral for 6 weeks. Int
Treatment - Drugs
Placebo
Intervention group: N - Acetylcysteine with trade name of mucomyst, as 600 milligram tablet, made by swiss zambon company, given twice daily (every 12 hours), per oral for 6 weeks.
control group : Placebo 600 mg twice daily ( per 12 hours ) oral use, at a duration of 6 weeks

Sponsors

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

Eligibility

Sex/Gender
All
Age
16 Years to 100 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: All of the chronic hemodialysis patients due to end stage renal disease more than 16 years old and at least three months has been past from starting of hemodialysis. Exclusion criteria: Every acute disease leads to hospitalization from one month before or during trial ; Allergy to N-acetylcysteine; Hepatic cirrhosis; Using vitamin E or C or every known antioxidant from 2 weeks before or during trial; Congestive heart failure or ejection fraction less than 35%; Not using of N- acetylcysteine or placebo more than 20% of total drug.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Hemoglobin. Timepoint: Before intervention and 6 weeks after intervention. Method of measurement: by cyanmet hb method as gr/dl with drabkin kit.;Hematocrit. Timepoint: Before intervention and 6 weeks after intervention. Method of measurement: By Santrifiuj micro hematocrit as persentage.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactBabak Alavian

Ahvaz Jondishapour University of Medical Sciences

Alavian.b@ajums.ac.ir; Dr_babakjj@yahoo.com+98 61 1374 3013

Outcome results

None listed

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