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The application of precise surgical cooperation under the concept of membrane anatomy in laparoscopic radical tumor resection: A randomized controlled study

The application of precise surgical cooperation under the concept of membrane anatomy in laparoscopic radical tumor resection: A randomized controlled study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600123403
Enrollment
Unknown
Registered
2026-04-26
Start date
2026-04-30
Completion date
Unknown
Last updated
2026-05-04

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

Conditions

Gastrointestinal tumor

Interventions

Intervention group:Precision surgery support, implemented on the basis of traditional nursing cooperation
Control group:Traditional intraoperative nursing cooperation

Sponsors

The Central Hospital of Wuhan
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1.The patient was diagnosed with gastric/colorectal malignant tumors through pathological biopsy, which met the surgical indications for laparoscopic radical resection under the concept of membrane anatomy; 2.The patient is over 18 years old, with no restrictions on gender; 3.There is no severe dysfunction of important organs such as the heart, liver, kidney, or lung, no abnormal coagulation function, and no surgical contraindications; 4.The patient voluntarily participates in this study and signs the informed consent form.

Exclusion criteria

Exclusion criteria: 1.Those with other malignant tumors, severe infections, or autoimmune diseases; 2.Those who received anti-tumor treatments such as radiotherapy, chemotherapy, or targeted therapy before the surgery; 3.Those whose surgeries were converted to open surgeries or whose surgical methods were changed; 4.Those with cognitive dysfunction or mental disorders and who cannot cooperate with the evaluation; 5.Those whose data collection is incomplete. 6.Those with cognitive dysfunction or mental disorders and who cannot cooperate with the research-related surveys; 7.Those whose clinical data are incomplete and cannot complete the collection of indicators.

Design outcomes

Primary

MeasureTime frame
Total duration of the surgery;Intraoperative blood loss;Error rate of endoscopic instrument transfer;Number of instrument transfers;The number of times the equipment fell;Average preparation time for equipment transfer;Postoperative time for rectal gas expulsion;Postoperative defecation time;Satisfaction of surgeons;Nurse work stress;

Countries

China

Contacts

Public ContactLi Li

The Central Hospital of Wuhan

33377525@qq.com+86 158 2725 3950

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: May 7, 2026