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The effect of ERAS for the prognosis of patients after esophagectomy, a prospective cohort study

The effect of ERAS for the prognosis of patients after esophagectomy, a prospective cohort study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1800016997
Enrollment
Unknown
Registered
2018-07-06
Start date
2018-08-01
Completion date
Unknown
Last updated
2018-07-09

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

Conditions

Esophageal cancer

Interventions

ERAS group:Enhanced recovery after surgery

Sponsors

Department of Cardiothoracic Surgery, Nanjing General Hospital of Nanjing Military Region
Lead Sponsor

Eligibility

Sex/Gender
Male
Age
20 Years to 79 Years

Inclusion criteria

Inclusion criteria: 1) Aged 20 to 80 years old man and woman; 2) Patients diagnosed as esophageal cancer by gastroscopy and pathology; no more than 7.5% of weight loss in the first three months of surgery; 3) No surgical contraindications, and R0 resection of esophageal cancer in our hospital; 4) Voluntarily participate in the study and sign an informed consent form; 5) Subjects can follow the drug dose and visit plan; 6) Can objectively describe the symptoms, no serious infection, respiratory insufficiency, etc., can actively cooperate; 7) Non-pregnant, lactating women;

Exclusion criteria

Exclusion criteria: 1) Those who do not meet the inclusion criteria, or who are judged by the competent physician to be unfit to participate in the trial; 2) The general situation is poor, the symptoms cannot be described objectively, or serious infections, respiratory insufficiency, etc. cannot be actively cooperated; 3) suffering from diabetes, thyroid dysfunction and other metabolic diseases; 4) There is a history of preoperative radiotherapy and chemotherapy; 5) severe postoperative complications (anastomotic fistula, pulmonary infection, etc.); 6) Patients who have participated in other clinical trials within 3 months prior to the trial; 7) Those who suffer from allergic diseases and are allergic to the body; have a history of drug sensitivity similar to the drug structure, and have a history of allergies to narcotic drugs; 8) sponsors or researchers or their family members who are directly involved in the trial; 9) The relevant information is incomplete during the study period; 10) The investigator believes that there is no reason for being selected.

Design outcomes

Primary

MeasureTime frame
Scored Patient-Generated Subjective Global Assessment;Quality of Life;Body composition analysis;albumin;Prealbumin;Transferrin;Hospital stay;

Secondary

MeasureTime frame
VAS;Hospital costs;Blood glucose;

Countries

China

Contacts

Public ContactYi Shen

Department of Cardiothoracic Surgery, Nanjing General Hospital of Nanjing Military Region

dr.yishen@163.com+86 13913907880

Outcome results

None listed

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