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Prospective randomized control trial of fast track surgery on postoperative gastrointestinal tumor

Prospective randomized control trial of fast track surgery on postoperative gastrointestinal tumor

Status
Active, not recruiting
Phases
Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-TRC-08000157
Enrollment
Unknown
Registered
2008-10-15
Start date
2008-05-01
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

GastrIc and intestinal cancer

Interventions

Regular group:Same as regular group.
Water before operation group:No lavation and nasogastric intubation. Oral intake of water 250ml 1.5-2 hours before operation
others are the same as regular group.
Fast track group:No lavation and nasogastric intubation and oral intake of water 250ml within 1.5-2 hours before operation
place nasojejunic feeding tube during operation
other approaches same as regular group.
Regular group:Preoperative fasting 6-8 hours, nasogastric intubation before operation
early ambulation in 24-48 hours, removing catheter at 48 hour after operation and control blood sugar under 12 mmol/l.
Glucose before operation:No lavation and nasogastric intubation. Oral 5% glucose solution 250ml within 1.5-2 hours before operation
other treatment same as regular group.
Fast track group:Place nasojejunic feeding tube in patients with gastric cancer during operation and others are the same as regular group.

Sponsors

The First Affiliated Hospital of Sun Yat-sen University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Age 18~80 years old male or female; 2. Malignant gatriintestinal tumor prepared for radical excision; 3. No obstruction of digestive tract; 4. Plasma albumen level >35g/L, hemoglobin concentration >90g/L before operation; 5. ASA grade I-II, cardiac function grade 1-2; 6. BMI>=18.5kg/?before operation; 7. Participants attend the trial of their own free will and able to understand the procedure and objective.

Exclusion criteria

Exclusion criteria: 1. Abnormality or defect in gastrointestinal function; 2. High risk in aspiratory regurgitation; 3. Water-electrolyte imbalance before operation; 4. Pregnant or breast-feeding women 5. Possible difficult airway; 6. Abnormality of endocrine hormone or medication of steroids.

Design outcomes

Primary

MeasureTime frame
Length of hospital stay after operation;

Secondary

MeasureTime frame
Anesthesia complication;Time before taking full meal;Immunology index;Nutrition index after operation;Insulin sensitivity after operation;Surgical complication;Time before defaecation;Stress index after operation;Time before far;

Countries

China

Contacts

Public ContactYulong He
ylh@medmail.com.cn+86 020 87331059

Outcome results

None listed

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