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Randomized, parallel control, double-blind, multi-center clinical trials for the effectiveness and safety of preoperative clinical use of malt-dextrindal fructose drinks

Randomized, parallel control, double-blind, multi-center clinical trials for the effectiveness and safety of preoperative clinical use of malt-dextrindal fructose drinks

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000032335
Enrollment
Unknown
Registered
2020-04-26
Start date
2017-06-20
Completion date
Unknown
Last updated
2020-04-27

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

Conditions

elective surgery

Interventions

A:Oral malt dextrin fructose liquid
B: Oral placebo

Sponsors

Tenth People's Hospital of Shanghai
Lead Sponsor

Eligibility

Sex/Gender
All
Age
40 Years to 70 Years

Inclusion criteria

Inclusion criteria: (1) General surgery option gastric cancer, colorectal, pancreatic duodenum removal surgery patients; (2) Initial treatment of patients; (3) Inpatients aged 45 to 70 years old men and women; (4) Voluntary signature of written informed consent; (5) Fast for 8-12 hours before surgery and 2 hours for drinking; (6) The length of hospital stay after surgery is greater than 72 hours; (7) The patient does not infuse the sugary solution during the procedure; (8) Digestive physician's participation in preoperative assessment of gastrointestinal function is normal.

Exclusion criteria

Exclusion criteria: (1) Patients who have been diagnosed with diabetes and other severe metabolic diseases; (2) Emergency surgery for patients; (3) Patients with gastric drainage disorder, digestive obstruction, gastroesophageal reflux, inability to use intestinal preparations; (4) Patients with severe cardio-renal insufficiency, etc., affected the safety evaluation of the trial; (5) People with mental disorders, alcohol dependence, and a history of substance abuse; (6) Women who are breastfeeding and pregnant; (7) People who are allergic to a variety of drugs or who have been allergic to a variety of drugs, those who are allergic to malt dextrin fructose; (8) Participants in other clinical studies 3 months prior to the trial; (9) Researchers do not consider it appropriate to be involved in this study.

Design outcomes

Primary

MeasureTime frame
Blood Glucose;fasting insulin;

Countries

China

Contacts

Public ContactHuanlong Qin

Shanghai Tenth People's Hospital

13801595388@163.com+86 13801595388

Outcome results

None listed

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