Clinical trial · Observational
Effects of Different Preoperative Oral Rehydration Protocols in Undergoing Thoracoscopic Radical Lung Cancer Surgery
Effects of Different Preoperative Oral Rehydration Protocols on Safety, Comfort, and Postoperative Outcomes in Elderly Patients Undergoing Thoracoscopic Radical Lung Cancer Surgery: A Randomized Controlled Trial
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
This study aims to compare the new preoperative oral rehydration protocol (administering 50-100 mL of clear fluids or carbohydrate-rich beverages orally every hour until the patient arrives at the operating room) with the traditional preoperative protocol (consuming 200-300 mL of water orally two hours prior to surgery). The objective is to investigate the effects of these two protocols on the safety (e.g., risk of reflux and aspiration), comfort (e.g., levels of hunger, thirst, and anxiety), gastric emptying status (as assessed by gastric ultrasound indicators), and postoperative outcomes (e.g., incidence of postoperative delirium, insulin resistance, and inflammatory factor levels) in elderly patients undergoing thoracoscopic lung cancer radical surgery. This research seeks to identify a more appropriate preoperative rehydration protocol for elderly lung cancer patients.
Conditions
Conditions (1)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Postoperative Delirium | — | UNRESOLVED | — |
Interventions
Interventions (0)
Data not yet available
Design
Arms and outcomes
Arms (3)
- label
- Control Arm
- description
- 2-hour Preoperative Ingestion of 200-300 mL clear water
- label
- Intervention Arm 1
- description
- Hourly Preoperative Ingestion of 50-100 mL clear water
- label
- Intervention Arm 2
- description
- Hourly Preoperative Ingestion of 50-100 mL 12.5% carbohydrate-containing beverages
Primary outcomes (4)
- measure
- postoperative delirium
- timeFrame
- One to three days after the operation
- description
- The Confusion Assessment Method - Short Form(CAM-S) scoring for postoperative delirium is as follows: Total score 20 points, 0-6 points :Mild delirium; 7-12 points:Moderate delirium; ≥13 points: Severe delirium.
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 65 Years
- Maximum age
- 80 Years
Show eligibility criteria text
Inclusion Criteria: 1. Elderly patients aged 65 or above who are scheduled to undergo thoracoscopic radical lung cancer surgery. 2. American Society of Anesthesiologists (ASA) classification levels II-III. 3. No severe cognitive impairment (Mini-Mental State Examination (MMSE) score ≥ 24). 4. Able to cooperate with the study and sign the informed consent form. Exclusion Criteria: 1. Combined with severe functional impairments of important organs such as the heart, liver, and kidneys. 2. Suffering from metabolic diseases such as diabetes and hyperthyroidism. 3. Having digestive system diseases such as gastric emptying disorders, dysphagia, and intestinal obstruction. 4. Allergic or intolerant to carbohydrates. 5. Had received treatments such as radiotherapy and chemotherapy before the surgery that might affect the research indicators. 6. Patients with mental disorders or cognitive dysfunction.
References
Publications (0)
Data not yet available