Prevention of a parastomal hernia with Stapled Mesh stomA Reinforcement Technique (SMART) in patients undergoing permanent colostomy

Status

Recruiting

Phases

Early Phase 1

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR2100042020

Enrollment

Unknown

Registered

2021-01-12

Start date

2020-01-01

Completion date

Unknown

Last updated

2021-04-12

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

Conditions

Parastomal hernia

Interventions

experimental group:Insert the mesh via SMART surgery during permanent colostomy

control group:Traditional colostomy without mesh insertion

Eligibility

Sex/Gender

All

Age

18 Years to 85 Years

Inclusion criteria

Inclusion criteria: 1. Select patients who are scheduled for open permanent terminal colostomy, whether they are malignant or benign diseases. 2. Patients aged 18-85 years. 3. The postoperative survival time was longer than 1 year. 4. Patients who signed informed consent. 5. Patients who can understand the research related questionnaire.

Exclusion criteria

Exclusion criteria: 1. Patients with poor general condition (ASA grade 4-5); 2. Emergency colostomy patients; 3. Patients with ileostomy; 4. Patients with abdominal infection; 5. Patients allergic to patch; 6. Patients with colostomy; 7. Patients with drug or alcohol abuse; 8. Patients with mental disorders.

Design outcomes

Primary

Measure	Time frame
Parstomal hernia;	—

Secondary

Measure	Time frame
Quality of life;Pain score;Surgical incision infection;Intestinal obstruction;Intestinal fistula;Colostomy necrosis;Colostomy stenosis;Colostomy infection;Patients with parastomal hernia requiring reoperation;mortality rate;	—

Countries

China

Contacts

Public ContactJunjia Zhu

Jiangyin People's Hospital

531342412@qq.com+86 13861667601

Outcome results

None listed

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