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Investigating the effect of potassium citrate in preventing of decrease GFR levels in patients with stage 3, 4 and 5 of CKD.

Investigating the effect of potassium citrate in preventing of decrease GFR levels in patients with stage 3, 4 and 5 of CKD.

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20250118064415N1
Enrollment
74
Registered
2025-01-26
Start date
2025-02-19
Completion date
Unknown
Last updated
2025-02-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Chronic kidney disease. Chronic kidney disease

Interventions

Intervention 1: Intervention group: The group receiving potassium citrate tablets will take them daily, with one to three doses, depending on the patients initial condition. The prescribed dose will b

Sponsors

Ahvaz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Minimum age of 18 years Chronic kidney disease stages 3, 4, and 5. Plasma bicarbonate level less than 20 mmol/L. Clinically stable condition. Consent to participate in the study.

Exclusion criteria

Exclusion criteria: Use of diuretics, potassium, or potassium supplements within the past 3 months. Chronic sepsis. Poorly controlled hypertension (>150/90 mmHg). Overt congestive heart failure (EF below 20%). Pregnancy and lactation. History of cystinuria. History of inflammatory bowel diseases. History of hyperparathyroidism. Use of warfarin. Use of vitamin or antioxidant supplements.

Design outcomes

Primary

MeasureTime frame
Change in GFR (Glomerular Filtration Rate). Timepoint: Measurements are taken before the intervention begins, followed by reassessment of GFR and the patients' clinical status in the second week, first month, third month, and finally at the sixth month after the intervention. Method of measurement: GFR will be re-measured using the Modified MDRD formula.

Secondary

MeasureTime frame
Adverse drug. Timepoint: Adverse events will be recorded after the intervention at the second week, first month, third month, and finally at the sixth month. Method of measurement: Adverse events will be recorded throughout the treatment period using a checklist approved by two specialists: a nephrologist and a pharmacologist.;Serum bicarbonate level. Timepoint: Measurements are taken before the intervention begins, followed by reassessment of serum bicarbonate levels in the second week, first month, third month, and finally at the sixth month after the intervention. Method of measurement: Potassium levels will be measured through blood sampling and laboratory testing.;Creatinine. Timepoint: Measurements are taken before the intervention begins, followed by reassessment of serum creatinine levels in the second week, first month, third month, and finally at the sixth month after the intervention. Method of measurement: Creatinine levels will be measured through blood sampling and laboratory testing.;Venous Blood Gas (VBG). Timepoint: Measurements are taken before the intervention begins, followed by reassessment of VBG levels in the second week, first month, third month, and finally at the sixth month after the intervention. Method of measurement: VBG levels will be measured through blood sampling and laboratory testing.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactNavid Najarpour

Ahvaz University of Medical Sciences

navid.najarpour@yahoo.com+98 61 3320 4574

Outcome results

None listed

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