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A multicenter, non-Intervention, cohort study of enhanced recovery after surgery (ERAS) clinical pathway in perioperative patients with ankle joint fracture

A multicenter, non-Intervention, cohort study of enhanced recovery after surgery (ERAS) clinical pathway in perioperative patients with ankle joint fracture

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR-ONC-17012808
Enrollment
Unknown
Registered
2017-09-26
Start date
2017-10-01
Completion date
Unknown
Last updated
2017-10-02

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

Conditions

ankle joint fracture

Interventions

Sponsors

Beijing Jishuitan Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
16 Years to 70 Years

Inclusion criteria

Inclusion criteria: (1) Aged 16-70 years old; (2) Meet the diagnostic criteria for ankle joint fracture; (3) Patients without severe underlying diseases in heart, brain, lung, kidney or other vital organs, and preoperative ASA grading of I to II; (4) Patients who volunteered to participate this study himseif, and signed informed consent.

Exclusion criteria

Exclusion criteria: (1) Preoperative ASA grading of III or above; (2) Patients with fractures in other bones; (3) Patients with old ankle joint fracture; (4) Patients with diabetes mellitus or other severe metabolic diseases; (5) Gastric emptying disorder (such as gastroesophageal reflux, history of chronic aspiration, delayed gastric emptying ), complete obstruction of digestive tract or patients who cant use enteral preparations; (6) Patients with underlying diseases, such as severe heart failure or severe renal insufficiencywhich will have an effect on the assessment of the safety of this study; (7) Patients with mental disorders, alcohol dependence or a history of drug abuse; (8) Pregnant or lactating women; (9) Allergic constitution or patients who are always allergic to a variety of drugs; (10) Other patients who were considered unsuitable for this study by researchers.

Design outcomes

Primary

MeasureTime frame
postoperative length of stay;hospital cost;postoperative complications;VAS score;time to first flatus;time to diet;nutritional status;intraoperational blood loss;30-rehospitalization rate;Satisfaction of patients and their families;

Countries

China

Contacts

Public ContactXinbao Wu

Beijing Jishuitan Hospital

wuxinbao_jst@126.com+86 13701265110

Outcome results

None listed

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