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Clinical and genetic studies of the association between incisional infection and malnutrition after abdominal surgery

Clinical and genetic studies of the association between incisional infection and malnutrition after abdominal surgery

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2400082464
Enrollment
Unknown
Registered
2024-03-29
Start date
2024-01-08
Completion date
Unknown
Last updated
2024-04-01

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

Conditions

Associated conditions requiring abdominal surgery

Interventions

Part I: Current Situation Study (no grouping, sample size of 600 people):No
Part II: Nested case-control study (based on observations) case group:No
Part II: Nested case-control study (based on observations) control group:No

Sponsors

The First Affiliated Hospital of Xinjiang Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 89 Years

Inclusion criteria

Inclusion criteria: Part1:(1) Common abdominal surgery patients (gastrointestinal surgery and hepatobiliary and pancreatic surgery);(2) age=18 years old, (3) complete clinical data, (4) informed consent, voluntary participation in this study. Part2:(1) Based on the types of high-risk groups identified in the first part of the study, malnourished patients in this type of population were selected; (2) Age= 18 years old; (3) Complete clinical data; (4) Informed consent, voluntary participation in this study.

Exclusion criteria

Exclusion criteria: Part1:(1) Those who are severely mentally abnormal or unable to cooperate with consciousness disorders; (2) Patients with infectious diseases, metabolic diseases and/or chronic diseases; (3) Those who undergo chemotherapy, radiotherapy and other special treatments before surgery and/or within 30 days after surgery; (4) Patients with postoperative stoma or concurrent anastomotic leakage. Part2:(1) Those who are severely mentally abnormal or unable to cooperate with consciousness disorders; (2) Patients with infectious diseases, metabolic diseases and/or chronic diseases; (3) Those who undergo chemotherapy, radiotherapy and other special treatments before surgery and/or within 30 days after surgery; (4) Patients with postoperative stoma or concurrent anastomotic leakage.

Design outcomes

Primary

MeasureTime frame
Incision infection;Differentially expressed genes;

Secondary

MeasureTime frame
Incision healing (mice).;

Countries

PRC

Contacts

Public ContactWANG Dan

School of Nursing, Xinjiang Medical University

253975116@qq.com+86 186 9018 7019

Outcome results

None listed

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