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Continuous quality improvement of preventive programs for perioperative venous thromboembolism in Chinese adults with abdominal hernia (CHAT-4)

Continuous quality improvement of preventive programs for perioperative venous thromboembolism in Chinese adults with abdominal hernia (CHAT-4)

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2300067268
Enrollment
Unknown
Registered
2023-01-02
Start date
2023-01-02
Completion date
Unknown
Last updated
2023-05-15

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

Conditions

Ventral Hernia

Interventions

Experimental group:Evaluation and prevention were carried out according to the procedure of Implementation Plan of Preliminary Screening for the Prevention of venous thromboembolism in patients underg
Control group:Take the guide as the implementation plan

Sponsors

Beijing Chaoyang Hospital, Capital Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Clinically confirmed abdominal hernia; 2. Aged range from 18 to 80 years, gender is not limited; 3. Centerlessness, insufficiency of lung, liver, kidney and other important organs, no contraindications to surgery; 4. Voluntary subjects (patients or family members sign informed consent).

Exclusion criteria

Exclusion criteria: 1. Patients with incarcerated abdominal hernia, bilateral hernia, type I hernia; 2. Chronic kidney disease; 3. Patients who have a history of allergies to multiple drugs or have recently suffered from allergies, and have used drugs known to have damage to major organs within 4 weeks; 4. Participated in other clinical researchers within 3 months; 5. Specific allergic constitution, especially sensitive to chemical synthetic materials; 6. Patients with mental illness; 7. Patients with serious diseases causing increased abdominal pressure (such as severe prostatic hyperplasia, constipation or chronic cough; Uncontrollable ascites caused by cirrhosis or tumor); 8. Patients with infected lesions or bacteremia in the surgical area.

Design outcomes

Primary

MeasureTime frame
VTE risk assessment rate;

Countries

China

Contacts

Public ContactWang Minggang

Beijing Chaoyang Hospital, Capital Medical University

wmgonly@126.com+86 139 1062 7381

Outcome results

None listed

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