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RecruitingNCT05890820Updated Jun 6, 2023

The Effect of Nutritional Risk Parameters on Postoperative Pulmonary Complications in Geriatric Thoracic Surgery Cases

An observational study in Lung Cancer, Nutrition, Healthy and Postoperative Complications, sponsored by Ankara Ataturk Sanatorium Training and Research Hospital. Recruiting at 1 site in Turkey. Open to participants aged 65 Years and older. Per ClinicalTrials.gov, last updated 2023-06-06.

Sponsored by Ankara Ataturk Sanatorium Training and Research Hospital · Observational

From the registry’s dates

  • Primary completion was expected by Sep 2023, 3 years ago, but the record still lists the study as recruiting.
Study type
Observational
Model
Case-control
Time perspective
Prospective
Enrollment
100
Ages
65 Years and older
Sex
All
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Study summary

Preoperative evaluation of nutritional status in geriatric patients with lung cancer and implementation of these practices in elective patients are very important in terms of reducing postoperative complications and accelerating hospital discharge. For this purpose, many nutritional assessments and measurements are used. Our aim in this study was to evaluate the relationship between preoperative nutritional status and postoperative pulmonary complications in patients undergoing thoracic surgery for geriatric lung cancer.

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Conditions studied

  • Lung Cancer
  • Nutrition, Healthy
  • Postoperative Complications
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In context

Postoperative Complications

1,233 studies on the registry are indexed under Postoperative Complications; 292 are open to participants now.

This study's planned enrollment of 100 is below the median of 254 across 519 observational studies indexed under Postoperative Complications.

Browse Postoperative Complications studies →

Lead sponsor

Ankara Ataturk Sanatorium Training and Research Hospital is the lead sponsor of 32 studies on the registry; 17 are open to participants now.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
65 Years and older
Sexes eligible
All
Sampling method
Probability sample

Study population

Patients over 65 years of age with lung malignancy and undergoing thoracic surgery.

Inclusion criteria

  • Patients over 65 years of age
  • Lung Cancer
  • Patients undergoing thoracic surgery

Exclusion criteria

Exclusion Criteria:

  • Refusal to participate in the study
  • Patients with a diagnosis of hematological malignancy
  • Patients with missing data required for research
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Study design

Observational model
Case-control
Time perspective
Prospective
Enrollment
100 participants (estimated)
Target follow-up
6 Months
Patient registry
Yes

Interventions

  • OtherPreoperative nutritional assessment

    Preoperative nutritional assessment and postoperative pulmonary complications

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What researchers measure

Primary outcomes

  1. FFMI - Fat-Free Mass Index

    FFMI is an abbreviation for lean mass index. It defines the amount of your muscle mass relative to height and weight. The FFMI is part of the well-known and similar BMI family of body indexes. The effect of FFMI values on postoperative patient stay, intensive care unit stay, complications and postoperative mobilization time in lung cancer patients will be evaluated. Each patient will be evaluated by measuring the preoperative FFMI value 24 hours before.

    Time frame: 24 hours

Secondary outcomes

  1. BMI (Body Mass Index)

    BMI is a measurement of a person's leanness or corpulence based on their height and weight, and is intended to quantify tissue mass. The effect of BMI values on postoperative patient stay, intensive care unit stay, complications and postoperative mobilization time in lung cancer patients will be evaluated. Each patient will be evaluated by measuring the preoperative BMI value 24 hours before.

    Time frame: 24 hours

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Study locations

1 of 1 sites recruiting
  • Ankara Atatürk Sanatoryum Education and Research Hospital
    Ankara, Keçioren 06290, Turkey
    • M. Ozgur Cirik, Assoc. Prof · Contact
    Recruiting
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References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jun 6, 2023, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT05890820
Lead sponsor
Ankara Ataturk Sanatorium Training and Research Hospital
Responsible party
Mustafa Özgür Cirik (Associate Proffessor, Ankara Ataturk Sanatorium Training and Research Hospital) — Principal investigator
First posted
Jun 6, 2023
Start date
May 30, 2023 (estimated)
Primary completion
Sep 30, 2023 (estimated)
Completion
Oct 30, 2023 (estimated)
Last update
Jun 6, 2023

Study contacts

Mustafa Özgür Cirik Cirik, Assoc Prof
Contact
dr.ozgurr@hotmail.com
903123677235
Ali Alagöz, Full Prof
Contact
mdalagoz@gmail.com
903123677235

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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