Kidney-protective Intervention With Salt Substitute After Kidney Tumor Surgery: a Single-center Randomized Controlled Study(KISS Study)

Status: Recruiting
Location: See location...
Intervention Type: Dietary supplement
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

This clinical trial is an open-label, randomized controlled study designed to evaluate the efficacyand safety of salt substitutes in protecting renal function after kidney tumor surgery, aiming toprovide dietary renal protection strategies for postoperative kidney tumor patients. lt will alsoassess the feasibility of salt substitute intervention. The primary research questions are: 1. Does a salt substitute diet significantly improve estimated glomerular filtration rate (eGFR) compared to a regular salt diet in postoperative kidney tumor patients? 2. What is the safety profile of salt substitute intervention in postoperative kidney tumor patients? 3. What is the compliance rate among postoperative kidney tumor patients using saltsubstitutes? 4. ls the salt substitute intervention feasible? Researchers will compare the intervention group (salt substitute diet) with the control group (regular salt diet) to determine whether salt substitutes effectively improve postoperative eGFR in kidney tumor patients. Participants will be required to: 1. Consume salt substitutes or regular salt daily while strictly adhering to WHO-recommendedsalt intake levels for 1 year. 2. Undergo scheduled baseline assessments at 1, 3, 6, and 12 months post-surgery, with 24-hoururine tests at months 1 and 6 to evaluate compliance. 3. Receive regular monitoring of blood electrolytes, eGFR, and other renal function indicators. 4. Document any adverse events or health status changes during the study period.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• Participants must meet all of the following criteria:

‣ Voluntary participation with signed informed consent from both the primary participant and all cohabiting family members, with commitment to study procedures and follow-up;

⁃ Age ≥18 years at enrollment (when signing informed consent), any gender;

⁃ Diagnosed kidney tumor patients who underwent radical nephrectomy or partial nephrectomy (no restrictions on surgical approach);

⁃ Preoperative eGFR \>60 ml/min/1.73m² (calculated by CKD-EPI equation);

⁃ Serum potassium \<4.8 mmol/L;

⁃ Predominantly home-based dietary habits (\>90% meals prepared at home, assessed via self-report);

⁃ Normal contralateral renal function at screening;

⁃ Normal cardiopulmonary and hepatic function:

Locations
Other Locations
China
Jinling Hospital, Affiliated Hospital of Medical School, Nanjing University, Nanjing
RECRUITING
Nanjing
Contact Information
Primary
Qu Le M.D
septsoul@hotmail.com
+86 15720625951
Time Frame
Start Date: 2025-04-24
Estimated Completion Date: 2027-12-31
Participants
Target number of participants: 200
Treatments
Experimental: Salt substitute
Participants will consume salt substitutes
No_intervention: Common salt
Participants will consume Common salt
Related Therapeutic Areas
Sponsors
Leads: Jinling Hospital, China

This content was sourced from clinicaltrials.gov