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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT05540249
Other study ID # 2019-ZX40
Secondary ID
Status Not yet recruiting
Phase N/A
First received
Last updated
Start date September 2022
Est. completion date January 2023

Study information

Verified date September 2022
Source China National Center for Cardiovascular Diseases
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Preoperative carbohydrates (CHO) supplement has been shown to alleviate postoperative insulin resistance (IR) in nondiabetic patients undergoing a variety of surgeries. However, it remains controversial whether preoperative CHO could yield similar effects in diabetic patients. Thus, the investigators design a randomized controlled trial investigating the impact of preoperative CHO on postoperative IR and clinical outcomes in diabetic patients undergoing cardiac surgery. The results of the study may give some clinical implications and further improve perioperative care for diabetic patients.


Description:

CHO supplement has been widely investigated in nondiabetic patients undergoing various surgeries. It has been proved that preoperative CHO could alleviate postoperative insulin resistance (IR) and improve patients' well-being in nondiabetic patients. However, whether preoperative CHO could yield similar effects in diabetic patients remains controversial. Till now, seldom has the administration of preoperative CHO been investigated in diabetic patients and few studies reported IR and postoperative recovery of diabetic patients undergoing cardiac surgery. The investigators present a prospective, single-center, single-blind, randomized, no-treatment controlled trial of preoperative CHO on diabetic patients undergoing off-pump coronary artery bypass grafting (OPCAB). A total of 62 patients will be enrolled and randomized to either Group CHO or Group control (CTRL). Patients in group CHO will receive CHO fluid containing 50 g of carbohydrates the evening before surgery (20:00-24:00) while their counterparts in Group CTRL will be fasted after 20:00 the evening before surgery. The primary endpoints are postoperative insulin resistance (IR) assessed via homeostasis model assessment (HOMA). The secondary endpoints are the potential mediators relating to IR including inflammatory factors and stress reactions assessed by serum cortisol. Exploratory endpoints are in-hospital clinical endpoints.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 62
Est. completion date January 2023
Est. primary completion date December 2022
Accepts healthy volunteers No
Gender All
Age group 18 Years to 75 Years
Eligibility Inclusion Criteria: 1. Previously diagnosed T2DM 2. Diagnosed with CAD with coronary angiography and indicated for OPCAB 3. Age between 18 and 75 years old 4. First operation in the morning and anesthesia induced around 8:00 5. Written informed consent by the patients Exclusion Criteria: 1. Combined with other heart diseases or vascular malformations that require surgery in addition to OPCAB 2. Presence of symptoms or signs of heart failure such as orthopnea, distended jugular vein, lower extremity edema, etc. 3. Reduced LVEF (lower than 50%) 4. Combined with gastroesophageal reflux 5. Combined with thyroid insufficiency requiring replacement therapy with levothyroxine 6. Combined with adrenal insufficiency requiring replacement therapy with corticosteroids 7. Refuse to participate.

Study Design


Intervention

Dietary Supplement:
carbohydrates
Patients will orally consume 355mL CHO after 20:00 the evening before surgery.

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
China National Center for Cardiovascular Diseases

Outcome

Type Measure Description Time frame Safety issue
Other Nausea or vomiting Nausea or vomiting requiring medical treatment such as ondansetron In-hospital period after surgery (up to day 5)
Other New-onset postoperative atrial fibrillation (POAF) POAF is defined as new onset atrial fibrillation lasting at least 10min on the electrocardiogram (ECG) monitor or atrial fibrillation that requires treatment with medication after surgery. In-hospital period after surgery (up to day 5)
Other Major adverse cardiovascular and cerebral events (MACCEs) A composite endpoints of all-cause death, non-fatal myocardial infarction, stroke. In-hospital period after surgery (up to day 5)
Other ICU length The length of patient's stay in the ICU In-hospital period after surgery (up to day 5)
Other Mechanical ventilation time Duration of patient ventilator-assisted breathing In-hospital period after surgery (up to day 5)
Primary Peri-operative Change from baseline HOMA-IR HOMA-IR = [blood insulin (mu/L) × Blood glucose (mmol/L)]/22.5 Before anesthesia induction
Primary Peri-operative Change from baseline HOMA-IR HOMA-IR = [blood insulin (mu/L) × Blood glucose (mmol/L)]/22.5 Immediately after surgery
Primary Peri-operative Change from baseline HOMA-IR HOMA-IR = [blood insulin (mu/L) × Blood glucose (mmol/L)]/22.5 The first morning after surgery
Primary Peri-operative Change from baseline HOMA-IR HOMA-IR = [blood insulin (mu/L) × Blood glucose (mmol/L)]/22.5 The second morning after surgery
Primary Peri-operative Change from baseline HOMA-IR HOMA-IR = [blood insulin (mu/L) × Blood glucose (mmol/L)]/22.5 The third morning after surgery
Primary Peri-operative Change from baseline HOMA-IR HOMA-IR = [blood insulin (mu/L) × Blood glucose (mmol/L)]/22.5 The fifth morning after surgery
Secondary Interleukin -1 (IL-1) Inflammatory factors The first morning after surgery
Secondary Interleukin-6 (IL-6) Inflammatory factors The first morning after surgery
Secondary Interleukin-8 (IL-8), Inflammatory factors The first morning after surgery
Secondary Interleukin-10 (IL-10), Inflammatory factors The first morning after surgery
Secondary Tumor necrosis fator-a (TNF-a) Inflammatory factors The first morning after surgery
Secondary High-sensitivity C-reactive protein (hs-CRP) Inflammatory factors The first morning after surgery
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