Comparing the Incidence of Parastomal Hernia After Mesenteric Molding Suturing and Non-molding Suturing in Colostomy Surgery
A Prospective Randomized Controlled Trial Comparing the Incidence of Parastomal Hernia After Mesenteric Molding Suturing and Non-molding Suturing in Colostomy Surgery
1 other identifier
interventional
234
0 countries
N/A
Brief Summary
\*\*Research Background\*\* Colostomy surgery is a common surgical procedure widely used for the treatment of various gastrointestinal diseases, including rectal cancer, ulcerative colitis, and Crohn's disease. Although this surgery can significantly improve patients' quality of life and prognosis, the incidence of postoperative complications, particularly parastomal hernia (PSH), is relatively high. PSH refers to the formation of an abdominal wall hernia around the stoma, with an incidence rate that can reach up to 50%. PSH not only affects patients' quality of life but can also lead to pain, stoma dysfunction, and the need for reoperation, increasing medical costs and patient burden. Therefore, how to effectively prevent PSH has become an important topic in clinical research. \*\*Epidemiology of Parastomal Hernia\*\* The incidence of PSH varies across different studies, ranging from 10% to 50%. This variation may be due to differences in study design, patient characteristics, and surgical techniques. A systematic review and meta-analysis showed that the incidence of PSH differs significantly among different surgical techniques, with higher rates observed in traditional non-molding suturing techniques. Another large cohort study found that the incidence of PSH varies among different age groups and patients with different underlying diseases, suggesting that PSH occurrence may be influenced by multiple factors. \*\*Risk Factors for Parastomal Hernia\*\*
- \*\*Advanced Age\*\*: Older patients have reduced tissue elasticity and muscle strength, making them more susceptible to PSH.
- \*\*Obesity\*\*: Obese patients have higher intra-abdominal pressure, increasing the risk of PSH.
- \*\*Smoking\*\*: Smoking impairs wound healing, increasing the risk of PSH.
- \*\*Chronic Obstructive Pulmonary Disease (COPD)\*\*: COPD patients often experience coughing and breathing difficulties, leading to increased intra-abdominal pressure and a higher risk of PSH.
- \*\*Diabetes\*\*: Diabetic patients have poorer wound healing capabilities, making them more prone to PSH.
- \*\*Malnutrition\*\*: Malnutrition impairs tissue repair, increasing the risk of PSH.
- \*\*Surgical Factors\*\*:
- \*\*Surgical Technique\*\*: Different surgical techniques have a significant impact on the incidence of PSH. Traditional non-molding suturing techniques, which lack support for the tissues around the stoma, have a higher incidence of PSH.
- \*\*Stoma Location\*\*: Improper stoma placement, such as outside the rectus abdominis muscle, increases the risk of PSH.
- \*\*Stoma Size\*\*: An oversized or undersized stoma can affect stoma function and increase the risk of PSH.
- \*\*Use of Mesh\*\*: Using synthetic or biological mesh can significantly reduce the incidence of PSH. However, the use of mesh may bring risks of infection and other complications.
- \*\*Postoperative Factors\*\*:
- \*\*Early Mobilization\*\*: Appropriate early mobilization promotes circulation and wound healing, but excessive activity can increase intra-abdominal pressure and the risk of PSH.
- \*\*Increased Intra-abdominal Pressure\*\*: Activities such as coughing, constipation, and heavy lifting can increase intra-abdominal pressure and the risk of PSH.
- \*\*Infection\*\*: Postoperative infections can impair wound healing and increase the risk of PSH. \*\*Prevention Strategies for Parastomal Hernia\*\*
- \*\*Improvement in Surgical Techniques\*\*:
- \*\*Mesenteric Molding Suturing\*\*: In recent years, mesenteric molding suturing has gained attention due to its potential advantages. Mesenteric molding suturing strengthens the support around the stoma, reducing the protrusion of abdominal contents and thus lowering the incidence of PSH. A retrospective study showed that patients who underwent mesenteric molding suturing had a significantly lower incidence of PSH compared to those who received traditional non-molding suturing. However, these studies are mostly retrospective and have certain biases and limitations, lacking high-quality prospective randomized controlled trials to validate these findings.
- \*\*Use of Mesh\*\*: Some studies have shown that using synthetic or biological mesh can significantly reduce the incidence of PSH. The mesh provides additional support, reducing the protrusion of abdominal contents and thus lowering the risk of PSH. However, the use of mesh may bring risks of infection and other complications, requiring a careful balance of benefits and risks.
- \*\*Postoperative Care\*\*:
- \*\*Early Mobilization Guidance\*\*: Appropriate early mobilization promotes circulation and wound healing, but excessive activity should be avoided to prevent increased intra-abdominal pressure.
- \*\*Avoidance of Increased Intra-abdominal Pressure\*\*: Patients should be advised to avoid activities that can increase intra-abdominal pressure, such as coughing, constipation, and heavy lifting.
- \*\*Infection Prevention\*\*: Keeping the stoma area clean and dry and promptly managi
Trial Health
Trial Health Score
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participants targeted
Target at P75+ for not_applicable
Started Dec 2024
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Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
October 30, 2024
CompletedFirst Posted
Study publicly available on registry
November 5, 2024
CompletedStudy Start
First participant enrolled
December 1, 2024
CompletedPrimary Completion
Last participant's last visit for primary outcome
October 1, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
January 1, 2026
CompletedNovember 19, 2024
November 1, 2024
10 months
October 30, 2024
November 18, 2024
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Incidence of PSH within one year postoperatively
Incidence of PSH within one year postoperatively, from CT or body check
1 year
Secondary Outcomes (3)
Incidence of stoma-related complications
1 year
Operative time and time to stoma function recovery
1 year
Quality of life assessment
1 year
Study Arms (2)
Regular
ACTIVE COMPARATORThe stoma surgery will be performed using conventional non-molding suturing techniques. The specific steps include: 1. Select an appropriate stoma site, typically within the rectus abdominis muscle. 2. Perform routine suturing around the stoma without additional mesentery shaping. 3. Form the stoma, ensuring a tight fit of the surrounding tissues.
Mesenteric Molding Suturing
EXPERIMENTALDuring the stoma surgery, the mesentery will be shaped and sutured to enhance the support around the stoma and reduce the risk of hernia formation. The specific steps include: 1. Select an appropriate stoma site, typically within the rectus abdominis muscle. 2. Separate the mesentery around the stoma and shape it into a sturdy support structure. 3. Use non-absorbable sutures to fix the shaped mesentery to the abdominal wall, forming a sturdy support structure. 4. Form the stoma on the support structure, ensuring a tight fit of the surrounding tissues.
Interventions
The stoma surgery will be performed using conventional non-molding suturing techniques. The specific steps include: 1. Select an appropriate stoma site, typically within the rectus abdominis muscle. 2. Perform routine suturing around the stoma without additional mesentery shaping. 3. Form the stoma, ensuring a tight fit of the surrounding tissues.
During the stoma surgery, the mesentery will be shaped and sutured to enhance the support around the stoma and reduce the risk of hernia formation. The specific steps include: 1. Select an appropriate stoma site, typically within the rectus abdominis muscle. 2. Separate the mesentery around the stoma and shape it into a sturdy support structure. 3. Use non-absorbable sutures to fix the shaped mesentery to the abdominal wall, forming a sturdy support structure. 4. Form the stoma on the support structure, ensuring a tight fit of the surrounding tissues.
Eligibility Criteria
You may qualify if:
- Age 18 years or older.
- Patients requiring colostomy surgery.
- Ability to provide written informed consent.
- Expected survival of more than one year.
- No severe comorbidities such as heart, lung, liver, or kidney dysfunction.
You may not qualify if:
- Pregnant or breastfeeding women.
- History of major abdominal surgery that could affect the development of PSH.
- Mental illness that impairs understanding of the study content and ability to give informed consent.
- Patients receiving immunosuppressive therapy or chemotherapy.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Dr.
Study Record Dates
First Submitted
October 30, 2024
First Posted
November 5, 2024
Study Start
December 1, 2024
Primary Completion
October 1, 2025
Study Completion
January 1, 2026
Last Updated
November 19, 2024
Record last verified: 2024-11
Data Sharing
- IPD Sharing
- Will not share