Clinical trial Recruiting at 1 site Observational Ages 18 and up

Combining nutrition checks and muscle measurements to predict outcomes after lung cancer surgery

Official title: Prognostic Value of Multimodal Nutritional Status and Sarcopenia Assessment for Postoperative Risk Stratification in Patients Undergoing Lung Cancer Surgery: A Prospective Cohort Study

Run by Ondokuz Mayıs University · NCT07500376 · Data updated 2026-11-12

This project will test whether combining nutrition tests and muscle scans can predict recovery, complications, and short-term outcomes in adults having lung cancer surgery.

More Sarcopenia trials

Quick facts

Study typeObservational
Ages18 Years and up
SexAll
Enrollment142 (estimated)
SponsorOndokuz Mayıs University
Academic / other
Drugs / interventionschemotherapy, immunotherapy
Locations1 site (Samsun, Samsun)
StatusRecruiting
StartedMarch 15, 2026
Main results expectedFebruary 15, 2027
Study endsMarch 15, 2027
Registry record updatedJuly 24, 2026
Trial IDNCT07500376 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Adults aged 18 or older scheduled for anatomical lung resection (lobectomy or segmentectomy) for primary lung cancer with a preoperative thoracic CT within 30 days and able to complete nutritional and ultrasound measurements are ideal candidates.

Probably not a fit

Patients with neoadjuvant therapy, emergency procedures, pneumonectomy, advanced/metastatic disease, or those lacking evaluable imaging or unable to complete measurements are unlikely to benefit from this protocol.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This is a prospective, single-center observational cohort of adults undergoing anatomical lung resection for primary non-small cell lung cancer. Nutritional status will be measured with serum biomarkers, inflammatory indices, and validated clinical nutrition scores, plus dietitian-led bioimpedance and functional testing. Sarcopenia will be measured from preoperative thoracic CT (muscle area and density) and ultrasound muscle thickness, with international consensus criteria applied. These multimodal measures will be related to postoperative complications, ICU need, length of stay, and short-term mortality.

Why it matters

Potential benefit: If successful, the approach could identify higher-risk patients so clinicians can target preoperative nutrition and muscle-strengthening interventions to reduce complications and shorten recovery.

How similar studies have gone: Previous studies have linked either sarcopenia or malnutrition to worse postoperative outcomes after thoracic surgery, but comprehensive multimodal combinations like this are relatively novel and not yet widely validated.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Age ≥18 years
* Patients undergoing anatomical lung resection (lobectomy or segmentectomy) for primary lung cancer
* Availability of preoperative thoracic computed tomography (CT) within 30 days before surgery
* Completion of preoperative nutritional assessment and ultrasonographic muscle measurements
* Ability to provide written informed consent

Exclusion Criteria:

* Receipt of neoadjuvant chemotherapy, immunotherapy, or radiotherapy
* Emergency surgery
* Pneumonectomy
* Combined resection of another organ during the same procedure
* Inadequate or non-evaluable imaging or measurement data
* Immunosuppressive therapy or presence of advanced/metastatic disease
* Significant thoracic deformity or prior conditions interfering with muscle measurements
* Refusal or inability to provide informed consent

Where it's running

  • Ondokuz Mayis University Faculty of Medicine, Department of Thoracic Surgery
    Samsun, Samsun, Turkey (Türkiye)
    Recruiting

Study contacts

Similar studies

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How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.