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The impact of different oral rehydration regimens before surgery on the safety, comfort and postoperative

The impact of different oral rehydration regimens before surgery on the safety, comfort and postoperative

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500104191
Enrollment
Unknown
Registered
2025-06-12
Start date
2025-06-15
Completion date
Unknown
Last updated
2025-06-16

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

Conditions

Postoperative delirium

Interventions

Intervention group 2:The intervention group 2 was orally given 50 - 100 ml of a beverage containing
Intervention group 1:The intervention group 1 was orally given 50 - 100 ml of water every hour before the operation
The control group:The control group was prohibited from eating solid food 6 hours before the operation, and was orally given 200 - 300 ml of water 2 hours before the op

Sponsors

Fujian Medical University Union Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
65 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Elderly patients aged >=65 years old who intend to undergo thoracoscopic radical lung cancer resection; 2. American Society of Anesthesiologists (ASA) grade II.-III.; 3. No severe cognitive impairment (Mini-Mental State Scale MMSE score >=24 points); 4. Able to cooperate with the study and sign the informed consent form;

Exclusion criteria

Exclusion criteria: 1. Combined with severe dysfunction of important organs such as heart, liver, and kidney. 2. Suffering from metabolic diseases such as diabetes mellitus and hyperthyroidism. 3. Digestive system diseases such as gastric emptying disorders, dysphagia, and intestinal obstruction. 4. Allergy or intolerance to carbohydrates. 5. Have received radiotherapy and chemotherapy and other treatments that may affect the research indicators before surgery. 6. Patients with mental illness or cognitive dysfunction.

Design outcomes

Primary

MeasureTime frame
The incidence of postoperative delirium;The amount of fluid in the stomach;insulin resistance;preoperative anxiety;

Secondary

MeasureTime frame
Perioperative hunger;C-reactive protein;The incidence of perioperative nausea and vomiting;Tumor necrosis factor -a;The incidence of reflux aspiration during the perioperative period;Interleukin-6;Perioperative thirst;

Countries

China

Contacts

Public ContactLin Nan

Fujian Medical University Union Hospital

117806006@qq.com+86 18518134145

Outcome results

None listed

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