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Perioperative Process Optimization of enhanced recovery after surgery (ERAS): A prospective non-randomized controlled study of the effects for glucose preconditioning on perioperative subjective comfort and blood glucose in traumatic fracture associated with diabetes

Perioperative Process Optimization of enhanced recovery after surgery (ERAS): A prospective non-randomized controlled study for the effects of glucose preconditioning on perioperative subjective comfort and blood glucose in traumatic fracture associated with diabetes

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR1900027514
Enrollment
Unknown
Registered
2019-11-17
Start date
2018-07-18
Completion date
Unknown
Last updated
2019-11-18

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

Conditions

Traumatic fracture associated with diabetes

Interventions

Experimental Group:Optimized perioperative fasting water management method group
Control Group:Traditional perioperative fasting water management method group

Sponsors

Beijing Jishuitan Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
16 Years to 70 Years

Inclusion criteria

Inclusion criteria: (1) traumatic orthopedic patients with diabetes; (2) Fasting at 0:00 on the day of surgery, and no drinking for n-hour before surgery (stomach emptying time); (3) Drink immediately after surgery and eat after 2 hours; (4) Patients who volunteered to participate this study himself, and signed informed consent.

Exclusion criteria

Exclusion criteria: (1) Severe metabolic diseases, emergency, gastrointestinal dysfunction, heart and kidney dysfunction or others should not be involved in patients; (2) Intraoperative bleeding>1000ml; (3) Special surgery such as pelvis; (4) patient with Mental disorders, alcohol dependence, history of drug abuse, allergies; (5) Lactating and pregnant patients; (6) 3 months before the trial, patients participated in other clinical studies; (7) Other patients who were considered unsuitable for this study by researchers.

Design outcomes

Primary

MeasureTime frame
Subjective comfort before and after surgery (anxiety, thirst, hunger, nausea, grip, fatigue, dizziness, sweating, stomach discomfort);

Secondary

MeasureTime frame
HR, BP before surgery, before anesthesia and after anesthesia;postoperative complications;Demand for water within 6 hours after surgery;

Countries

China

Contacts

Public ContactXu Sun

Beijing Jishuitan Hospital

chunxia.zhang@unimedsci.com+86 010-58516809

Outcome results

None listed

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