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The effect of Carnitine on plasma Albomin level in haemodialysis patient

The effect of Carnitine on plasma Albomin level in haemodialysis patient in Alzahra hosptalin Isfahan

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT138804092106N1
Enrollment
22
Registered
2010-04-27
Start date
2008-10-22
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

haemodialysis patients. End-stage renal disease

Interventions

Sponsors

Isfahan university of medical sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
21 Years to 100 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: age upper than 21, have history of haemodialysis at least for one month before, having informed consent, no history of carnitine use in previous 8 weeks, no history of infectious disease or fever in previous month. Exclusion criteria: having side effects after taking tablets (like hypertension, dizziness, blurred vision, minimental status and diarrhea), person who want to exit from the staudy,having an infectious problem or antibiotic usage or if a patient change the dialysis method, migrate from the center, having renal transplantation .

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Albomin of plasma. Timepoint: 1 month. Method of measurement: Bromocrosol Green method.

Secondary

MeasureTime frame
Side effects. Timepoint: evrey month. Method of measurement: questionnair.;Hemoglobin. Timepoint: every month. Method of measurement: automated analyzer.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactAfrooz Eshaghian

Isfahan university of medical scieces

eshaghian@edc.mui.ac.ir+98 31 1236 7247

Outcome results

None listed

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