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Effect of intravenous vitamin C on sleep Quality in Hemodialysis patients

Effect of intravenous vitamin C on sleep Quality in Hemodialysis patients

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT138905174365N3
Enrollment
60
Registered
2010-12-11
Start date
2010-10-05
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. Extracorporeal dialysis

Interventions

Intervention 1: Intervention group receives vial vit C 500mg/5cc intravenously at the end of hemodialysis 3 times a week for a period of 8 weeks. Intervention 2: Control group receives 5cc Normal Sali
Treatment - Drugs
Placebo
Intervention group receives vial vit C 500mg/5cc intravenously at the end of hemodialysis 3 times a week for a period of 8 weeks
Control group receives 5cc Normal Salin at the end of hemodialysis 3 times a week for a period of 8 weeks

Sponsors

Mazandaran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 70 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: Signing informed consent, Being on hemodialysis three times a week for at least 6 months prior to the study, age 20-70 years old. Exclusion criteria: Refusal at any time to continue the study, History of Infectious diseases and hospitalization within 2 months prior to the trial, History of vit E, vit C, alcohol & oil fish consumption within 2 months prior to the trial, History of renal transplantation, History of immunosuppressive drugs consumption within 2 months prior to the trial, History of severe neuropsychology, cardiac, respiratory, liver disease or malignancy, Systemic disease during the study

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Sleep quality. Timepoint: before intervention and two months later. Method of measurement: PSQI=Pittsburgh sleep quality index.

Secondary

MeasureTime frame
Serum CRP. Timepoint: before intervention and two months later. Method of measurement: mg/l-laboratory kit.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactAmir Emami Zeidi

Mazandaran University Of Medical Sciences

amie_ei@yahoo.com+98 15132612458

Outcome results

None listed

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