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Protective effects of salvianolate on contrast-induced nephropathy after primary percutaneous coronary intervention: a multi-centre clinical trial

Protective effects of salvianolate on contrast-induced nephropathy after primary percutaneous coronary intervention: a multi-centre clinical trial

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-IPR-16010073
Enrollment
Unknown
Registered
2016-12-02
Start date
2014-12-01
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

contrast-induced nephropathy

Interventions

salvianolate group:Intravenous salvianolate (400mg+0.9% normal saline 500ml, a rate of 100ml/h) during the procedure, followed by continues infusion (400mg+0.9% normal saline 250ml, a rate of 100ml/h)
narmal saline hydration group:Intravenous hydration with normal saline at a rate of 1ml/kg/h during the procedure and lasting for 12h after primary PCI

Sponsors

Shanghai Sixth People's Hospital Affiliated to Shanghai Jiao Tong University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
25 Years to 90 Years

Inclusion criteria

Inclusion criteria: 1. Patients who were diagnosed with STEMI, NSTEMI or high-risk ACS underwent emergency coronary angiography and primary PCI; 2. Patients met the indication for emergency coronary angiography and primary PCI.

Exclusion criteria

Exclusion criteria: 1. In a critical condition or other conditions which might seriously impact treatment outcomes and prognosis on admission, such as cardiogenic shock, congestive heart failure (New York Heart Association class IV), severe renal or hepatic insufficiency (e.g. cirrhosis, pre-existing end-stage renal disease requiring dialysis), active gastrointestinal bleeding, acute stroke and terminal malignancies; 2. Being considered not suitable for procedure by operation group, such as contraindication to antiplatelet therapy, mental disorder, fever of undetermined origin (>38.5 degree C), uncontrolled infection and severe wasting; 3. Allergic to contrast agent or salvianolate; 4. Pregnancy or lactation; 5. Other conditions determined by researchers should be excluded.

Design outcomes

Primary

MeasureTime frame
serum creatinine;eGFR;Cys C;the incedence of CIN;

Countries

China

Contacts

Public ContactLu Zhigang

Shanghai Sixth People's Hospital Affiliated to Shanghai Jiao Tong University

zhugang_lu@126.com+86 18930177619

Outcome results

None listed

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