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Effect of perioperative sequential insulin therapy on blood glucose control in patients with non insulin dependent type 2 diabetes undergoing total joint replacement: a prospective randomized controlled study

Effect of perioperative sequential insulin therapy on blood glucose control in patients with non insulin dependent type 2 diabetes undergoing total joint replacement: a prospective randomized controlled study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400082636
Enrollment
Unknown
Registered
2024-04-02
Start date
2024-04-08
Completion date
Unknown
Last updated
2024-04-08

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

Conditions

End stage hip and knee joint disease associated with diabetes

Interventions

Group 1:Maintain pre admission oral hypoglycemic medication regimen (use regular insulin as a remedy when blood sugar control is poor)
Group 2:Stop taking oral hypoglycemic drugs and use the basal mealtime insulin regimen. The total daily insulin dose is 0.5U/kg, with basal insulin accounting for half of the total dose. The remaining
Group 3:Stop taking oral hypoglycemic drugs and use a slide insulin regimen, with insulin dosage adjusted according to a predetermined regimen

Sponsors

West China Hospital of Sichuan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: Patients who are admitted to the hospital and plan to undergo the first total joint replacement surgery, whose blood sugar level is between 140~400mg/dl, who have a history of diabetes for more than 3 months, who are between 18 and 80 years old, who have received simple diet treatment, any oral hypoglycemic drugs or small dose (daily dose less than 0.4U/kg) insulin treatment before admission

Exclusion criteria

Exclusion criteria: Hyperglycemia without a known history of diabetes, type 2 diabetes requiring large dose (daily dose = 0.4U/kg) of insulin control, inappropriate adjustment of hypoglycemic program after consultation with endocrinologists, cardiac surgery, clinically related liver disease or renal function impairment (serum creatinine 3.0 mg/dL), history of diabetes ketoacidosis, pregnancy, and any mental condition leading to the inability of subjects to make informed consent

Design outcomes

Primary

MeasureTime frame
Blood glucose level;Frequency of hypoglycemia ;

Secondary

MeasureTime frame
Number of patients using insulin for remedial purposes;Insulin salvage dosage;Hospital stay;Complication;Patient satisfaction;

Countries

China

Contacts

Public ContactZhou Zongke

West China Hospital of Sichuan University

zhouzongke@scu.edu.cn+86 189 8060 1028

Outcome results

None listed

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