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Application value of the modified "one-needle technique" in laparoscopic radical rectal resection with prophylactic ileostomy: a retrospective cohort study

Application value of the modified "one-needle technique" in laparoscopic radical rectal resection with prophylactic ileostomy: a retrospective cohort study

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600122597
Enrollment
Unknown
Registered
2026-04-15
Start date
2026-04-15
Completion date
Unknown
Last updated
2026-04-20

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

Conditions

Patients undergoing laparoscopic radical resection of the rectum who require prophylactic ileostomy are evaluated for the advantages and disadvantages of the modified "one-stitch" ostomy method versus the traditional ostomy method.

Interventions

Observation group (modified "one-needle method". Using the modified "one-stitch" stoma method):None
Control group (traditional loop stoma. The modified "one-stitch" stoma technique is not selected.):None

Sponsors

The First Affiliated Hospital of the Baotou Medical College of Inner Mongolia University of Science and Technology
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1.Disease diagnosis: Confirmed as rectal cancer by pathology examination and underwent laparoscopic radical resection for rectal cancer. 2.Surgical approach: Prophylactic double-barrel ileostomy was performed simultaneously during the surgery, and the ileostomy closure was carried out by the same group of surgeons at the same hospital within 6 months postoperatively. 3.Ostomy method: Based on the study grouping, clearly adopt one of the following two methods: Modified group: Using the "modified one-stitch method" Control group: Using the "traditional ostomy method"; 4.Clinical Complete clinicopathological data, with a postoperative follow-up period of at least 6 months. Follow-up should be completed by at least June 2025.

Exclusion criteria

Exclusion criteria: 1.Emergency surgery: for those who undergo emergency surgery due to intestinal obstruction, perforation, etc. 2.Multivisceral resection: During the operation, simultaneous resection of other organs such as the liver, spleen, and urinary bladder is performed. 3.Distant metastasis: Patients who undergo palliative resection only when distant metastasis (Stage IV) is found preoperatively or intraoperatively. 4.Severe underlying diseases: those who have been using glucocorticoids or immunosuppressive agents for a long time. Those with combined diabetes mellitus and extremely poor blood sugar control (fasting blood glucose > 11.0 mmol/L). Those with combined severe hypoproteinemia (albumin < 30 g/L) or severe anemia (hemoglobin < 70 g/L) that has not been corrected. 5.Previous abdominal surgical history: There is a history of lower abdominal surgery that has caused severe abdominal cavity adhesion, affecting the stoma operator. 6.Patients with pre-existing chronic inflammatory bowel diseases (such as Crohn's disease, ulcerative colitis) or severe skin conditions. 7. Loss to follow-up: Patients who were lost to follow-up within 6 months postoperatively and whose information on stoma complications could not be obtained.

Design outcomes

Primary

MeasureTime frame
General information, surgical data, and postoperative data of the patients.;Stoma-related complications;

Secondary

MeasureTime frame
Time of first surgery;

Countries

China

Contacts

Public ContactLi Jin

The First Affiliated Hospital of the Baotou Medical College of Inner Mongolia University of Science and Technology

lijin-0472@163.com+86 472 217 8741

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Apr 23, 2026