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Effects of preoperative oral carbohydrate on functional recovery after ESD in patients with early gastric cancer

Effects of preoperative oral carbohydrate on functional recovery after ESD in patients with early gastric cancer

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200063748
Enrollment
Unknown
Registered
2022-09-15
Start date
2022-09-15
Completion date
Unknown
Last updated
2023-04-17

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

Conditions

Early gastric cancer

Interventions

Experimental group :Oral carbohydrate intake before ESD

Sponsors

Shanghai Tenth People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. 18 years old <= age <= 65 years old, gender is not limited; 2. BMI 18.5-23.9 kg/m2; 3. ESD surgery for early gastric cancer; 4. No distant lymph nodes and blood metastasis were found in the imaging data, and all met the indications for surgery and anesthesia; 5. ASA grade I-III; 6. All selected participants agree to participate in this study and sign.

Exclusion criteria

Exclusion criteria: 1. Patients with impaired gastrointestinal function, gastric emptying disorder, pyloric obstruction, gastroesophageal reflux or risk of aspiration; 2. Patients with severe cardiopulmonary diseases, blood diseases, coagulation disorders and taking anticoagulants; 3. Diabetic patients; 4. Patients admitted to ICU after operation; 5. Has been selected into other RCT trials; 6. The patient himself or the legally authorized person is unwilling to participate in the trial.1. Patients with impaired gastrointestinal function, gastric emptying disorder, pyloric obstruction, gastroesophageal reflux or risk of aspiration; 2. Patients with severe cardiopulmonary diseases, blood diseases, coagulation disorders and taking anticoagulants; 3. Diabetic patients; 4. Patients admitted to ICU after operation; 5. Has been selected into other RCT trials; 6. The patient himself or the legally authorized person is unwilling to participate in the trial.

Design outcomes

Primary

MeasureTime frame
Total complication rate;

Secondary

MeasureTime frame
Postoperative comfort index;Operation time and hemostasis time;Gastrointestinal recovery;Serum biochemicals;Length of stay and cost of stay;

Countries

China

Contacts

Public ContactHan Ting

Shanghai Tenth People's Hospital

253255849@qq.com+86 18917683618

Outcome results

None listed

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