Assessment of Relationship Between Preoperative Nutritional Status and Perioperative/Postoperativ… (NCT05417672) | Clinical Trial Compass
UnknownNot Applicable
Assessment of Relationship Between Preoperative Nutritional Status and Perioperative/Postoperative Conditions in Patients With Lung Cancer Scheduled for Lobectomy
Turkey (Türkiye)63 participantsStarted 2021-09-29
Plain-language summary
Malnutrition is common in patients with lung cancer. In patients with malnutrition risk, the risk of complications is high both in the perioperative, early and late postoperative periods. Malnutrition is an independent risk factor for length of hospital stay and cost in these patients. Patients with lung cancer may have many morbidities in postoperative period, especially problems with wound healing. Therefore, assessment of the nutritional status of patients with lung cancer should begin at the diagnosis stage.
Who can participate
Age range
18 Years
Sex
ALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion Criteria:
* Having a diagnosis of lung cancer
* Lung lobectomy operation will be performed
* 18 years and older patients
* Having an American Society of Anesthesiologists score of 1, 2, 3
* Having approved and signed the informed consent form
Exclusion Criteria:
* Patients who underwent lobectomy with a diagnosis other than lung cancer
* Patients younger than 18 years
* Patients with an American Society of Anesthesiologists score of 4 and above
* Patients who did not accept informed consent
* Patients who refused to participate in the study
Questions worth asking your doctor
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
Questions for the trial coordinator
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
What they're measuring
1
Postoperative complications
Timeframe: a month after the surgery
2
Length of stay in the intensive care unit
Timeframe: up to 30 days
3
Length of hospital stay
Timeframe: up to 30 days
4
Intraoperative hemodynamic complications
Timeframe: during the procedure
Trial details
NCT IDNCT05417672
SponsorTurkish Society of Anesthesiology and Reanimation