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Construction of a nutritional management plan for high-volume patients with enterostomy based on the KTA model

Construction of a nutritional management plan for high-volume patients with enterostomy based on the KTA model

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600121885
Enrollment
Unknown
Registered
2026-04-07
Start date
2026-04-15
Completion date
Unknown
Last updated
2026-04-14

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

Conditions

Rectal cancer

Interventions

Experimental group:Nutrition management plan for high-volume enterostomy patients based on the KTA model
Control group:Routine patient care and postoperative nutritional education.

Sponsors

The First Affiliated Hospital of Zhejiang University School of Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Age >=18 years 2. Patients with intestinal stoma excretion volume exceeding 1.5L - 2L per 24 hours for three consecutive days 3. Patients who are aware of their condition Possess good communication skills 4.Patients who have not received radiotherapy or chemotherapy before the surgery 5. Participants who have given informed consent and are willing to participate.

Exclusion criteria

Exclusion criteria: 1. Those who undergo another colostomy surgery due to recurrence, metastasis, or colostomy complications 2. Patients with severe anemia 3. Those with severe mental disorders 4. Those with hearing impairment 5.Patients with metabolic or immune-related diseases: such as complications like intestinal obstruction/intestinal ischemia, active inflammatory bowel disease in the acute stage, advanced malignant tumors (with an expected survival of less than 3 months), severe liver or kidney dysfunction (Child-Pugh C grade or eGFR < 30), those receiving parenteral nutrition support, or using drugs that affect intestinal motility (such as long-term opioids).

Design outcomes

Primary

MeasureTime frame
PG-SGA;Albumin;Hemoglobin;Serum potassium;Sodium ion in blood;Readmission rate of patients;

Secondary

MeasureTime frame
Human body measurement indicators;

Countries

China

Contacts

Public ContactQin Wang

The First Affiliated Hospital of Zhejiang University School of Medicine

wangqin308@126.com+86 138 5813 3469

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Apr 17, 2026