The effect of perioperative glucose-containing solution for non-diabetical patients following orthopaedic spinal surgery

Status

Active, not recruiting

Phases

Early Phase 1

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR1900022397

Enrollment

Unknown

Registered

2019-04-09

Start date

2019-05-01

Completion date

Unknown

Last updated

2019-04-15

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

Conditions

orthopaedic spinal surgery

Interventions

1:the glucose-containing(2%) solution intravenously

2:the glucose-containing(2%) solution with 0.8U/h intravenously

Eligibility

Sex/Gender

All

Age

18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1) ASA Classification Ito II; 2) Aged 20-70 years; 3) Orthopaedic surgery; 4) Operation time > 3 hours; 5) General anesthesia.

Exclusion criteria

Exclusion criteria: 1) hypertension; 2) neurological block; 3) cortisol and other hormones treatment; 4) ICU admission; 5) coagulation disease; 6) severe cardiopulmonary disease; 7) severe liver and kidney disease; 8) diabetes or preoperative abnormal blood sugar (>10 mmol/L, < 2.2 mmol/L); 9) Not agree to participate in the experiment.

Design outcomes

Primary

Measure	Time frame
perioperative blood glucose;	—

Secondary

Measure	Time frame
postoperative insulin asistance;?????? Postoperative pain score;postoperative PONV score;Postoperative functional recovery score;	—

Countries

China

Contacts

Public ContactPing Zhao

zhaoping_sj@icloud.com+86 18940258971

Outcome results

None listed

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