Post-operative Medium Chain Triglyceride Diet May Reduce Hospital Stay Following Lung Resection
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: MCT Diet.
- Who it may be relevant to
- Registry conditions: Thoracic Neoplasms. Basic parameters: 18 years — 80 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- Hong Kong
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
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Overview
Lung resection, a critical treatment for various thoracic diseases, including lung cancer, often necessitates prolonged hospitalization due to rare but severe postoperative complications such as chyle leaks, with an occurrence of 0.25%-3%, prolonging chest drainage, and delaying recovery. Therefore, effective postoperative care is essential for optimizing outcomes, reducing complications, and expediting recovery. Recent studies have highlighted the significant potential of medium-chain triglyceride (MCT) diets, owing to their unique absorption pathway and metabolic properties. MCT contains mainly medium-chain fatty acids (MCFA), which is absorbed in the intestine and transported to the liver via the portal system instead of the lymphatic system. This helps to bypass the lymphatic system, thereby reducing the volume of lymph. MCFAs also provide better energy utilization in stressed condition since it does not require carnitine shuttle upon metabolism, which is beneficial to post-operation recovery. Several studies have demonstrated the benefits of MCT diets in managing chyle leaks and supporting gastrointestinal recovery, particularly in conditions that strain the lymphatic system. For instance, short-term MCT-enriched diets have been associated with improved post-operation recovery of gastrointestinal, hepatic and renal functions, reduced total chest drainage volumes, and shorter hospital stay when compared to regular diet groups. Patients with post-operative chyle leak following thoracic surgery are often given an MCT diet to reduce chest drain volume and hence shorten hospital stay. Based on the successful use of MCT diet on patients with chyle leak after lobectomy, it is hypothesized that patients with chylothorax provided with post-operative MCT diet can also shorten hospital stay by decreasing chest drainage. Therefore, a prospective and randomized trial is designed to investigate how post-operative MCT diet in lung resection patients without chylothorax may affect hospital stay and post-operative recovery.
Detailed description
This study is a single-center, prospective, randomized trial designed to investigate how a post-operative diet enriched with MCT affects recovery in patients undergoing video-assisted thoracic surgery (VATS). Medical students from the Chinese University of Hong Kong, under the supervision of the principal investigator, will conduct the study, including obtaining consent and collecting data. Experienced surgeons at the Prince of Wales Hospital will perform the VATS procedures.
2.2 Hypotheses
1. MCT diet can speed up post-operative recovery and shorten hospital length of stay. 2. MCT diet poses no adverse effects in post-operative recovery for patients without chyle leak following lung surgery. 3. The use of MCT diet after discharge for 2 weeks can enhance patient recovery and possibly reduce readmissions or complications.
Interventions
- Dietary supplement MCT Diet
MCT diet for patients following lung resection
Primary outcome measures
- hospital length of stay (LOS) [Time frame: From the end of the lung resection procedure until the time of patient discharge, assessed up to 7 days post-surgery]
Secondary outcome measures (5)
- Total Chest Drain Output (mL) [Time frame: From the end of the lung resection procedure until the time of chest drain removal assessed up to 7 days post-surgery]
- Patient Satisfaction and Tolerability [Time frame: Upon discharge (assessed up to 7 days post-surgery), 2 weeks post discharge, 3 months post discharge]
- Number of Participants with Symptoms Associated with MCT Diet [Time frame: Upon discharge (assessed up to 7 days post-surgery), 2 weeks post discharge, 3 months post discharge]
- Number of patients with Infection symptoms [Time frame: Upon discharge (assessed up to 7 days post-surgery), 2 weeks post discharge, 3 months post discharge]
- Number of patients with infection risk [Time frame: Upon discharge (assessed up to 7 days post-surgery), 2 weeks post discharge, 3 months post discharge]
Eligibility criteria
Inclusion criteria
General Inclusion Criteria for All procedures:
- Age between 18 - 80 years
- Body mass index <35 kg/m2
- Suitable for minimally invasive surgery
- Willingness to participate as demonstrated by giving informed consent
Project-specific Criteria:
1\. Patients performed lobectomy with lymph node dissection
Exclusion criteria
Patient general exclusion criteria:
- Contraindication to general anesthesia
- Severe concomitant illness that drastically shortens life expectancy or increases the risk of therapeutic intervention
- Untreated active infection
- Non-correctable coagulopathy
- Emergency surgery
- Vulnerable population (e.g. mentally disabled, pregnancy)
Project-specific Criteria
- Segmentectomy
- Pleurodesis
- Esophageal procedures
- Redo/readmitted patients for lung resection
- Chylothorax (Triglyceride > 110 mL, excluded at day 1 routine lab check)
- Air leak (> 30 mL/min when back to ward)
- Heart Failure
- Renal failure (estimated GFR < 30; CKD grading stage 4-5)
- Moderate to severe adhesion (defined at randomization by surgeon; criteria include estimated surface area of adhesion and staging)
- History of tuberculosis or empyema
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: No
Study design
- Allocation
- Randomized
- Model
- Parallel assignment
- Masking
- Open label
- Primary purpose
- Supportive care
Study locations
Hong Kong · 1 center
- Prince of Wales Hospital — Shatin
Identifiers
NCT: NCT07159659 · MCT Study Protocol version 1.1