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The effects of trehalose on CABG patient

Evaluation of the effectiveness of trehalose on inflammatory factors, cardiac biomarkers and clinical outcomes after coronary artery bypass graft (CABG) surgery: A double-blind randomized controlled clinical trial

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20201129049534N11
Enrollment
90
Registered
2025-06-26
Start date
2025-08-06
Completion date
Unknown
Last updated
2025-07-21

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

Conditions

Cardiovascular disease. Presence of aortocoronary bypass graft

Interventions

Intervention 1: Intervention group: Patients who receive three sachets daily, each containing 10 grams of trehalose purchased from Shaanxi Fruiterco Biotechnology Co., Ltd. China, for 5 days (total of

Sponsors

Esfahan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
30 Years to 80 Years

Inclusion criteria

Inclusion criteria: Non-emergency coronary artery bypass surgery Age 30-80 years Gastrointestinal normal function and with intestinal or oral nutrition criteria Ejection fraction (EF) above 30% Arrest Time (cardiac resuscitation) 30 to 90 minutes Willingness to participate in the study and complete the consent form before surgery

Exclusion criteria

Exclusion criteria: Taking herbal supplements (as a supplement) during 3 months before the operation Requires balloon pump Adding another operation in addition to coronary artery bypass surgery(CABG), like simultaneous valve operation Patients with a history of underlying disease such as congenital and immune disorders and pancreatitis Diabetic patients who require insulin injections to control blood sugar or have uncontrolled diabetes. Pregnancy and lactation

Design outcomes

Primary

MeasureTime frame
C reactive Protein (CRP). Timepoint: At baseline (before the start of the intervention) and on the fifth day (end of the intervention). Method of measurement: ELISA test.;Lactate Dehydrogenase (LDH). Timepoint: At baseline (before the start of the intervention) and on the fifth day (end of the intervention). Method of measurement: ELISA test.;Interleukin 6 (int-6). Timepoint: At baseline (before the start of the intervention) and on the fifth day (end of the intervention). Method of measurement: ELISA test.;Creatine Kinase-MB. Timepoint: At baseline (before the start of the intervention) and on the fifth day (end of the intervention). Method of measurement: ELISA test.;Atrial fibrillation. Timepoint: On the fifth day (end of the intervention). Method of measurement: Electrocardiogram (ECG or EKG).

Secondary

MeasureTime frame
28-days mortality rate. Timepoint: 28 days after coronary artery bypass surgery. Method of measurement: Mathematically dividing the number of dead people by the total number of people using hospital records or telephone follow-up.;Fasting Blood Sugar. Timepoint: At baseline (before the start of the intervention) and on the fifth day (end of the intervention). Method of measurement: Photometric.;Cell Blood Count. Timepoint: At baseline (before the start of the intervention) and on the fifth day (end of the intervention). Method of measurement: Auto hematology analyzers.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMohammad Bagherniya

Esfahan University of Medical Sciences

heart@med.mui.ac.ir+98 31 3260 0961

Outcome results

None listed

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