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Relationship Between Hand Dynamometer Measurements, PFT, and mFI With Postoperative Outcomes

A

Atatürk Chest Diseases and Chest Surgery Training and Research Hospital

Status

Not yet enrolling

Conditions

Lung Cancer
Complication,Postoperative

Treatments

Other: Modified Frailty Index
Diagnostic Test: Pulmonary Function Test
Device: Hand Dynamometer

Study type

Observational

Funder types

Other

Identifiers

NCT06338007
2012-KAEK-15/2702

Details and patient eligibility

About

The study will take place at SBÜ Ankara Atatürk Sanatorium Training and Research Hospital and will include 100 patients over the age of 40 who are scheduled for lung malignancy surgery after 01 April 2024. Informed consent will be obtained from all patients, who will be assigned a number from 1 to 100.

For patients over 40 years of age who are scheduled to undergo lung malignancy resection surgery, demographic data including age, gender, height, weight, body mass index (BMI), diagnosis, comorbidities, and ASA (American Society of Anaesthesiologist) score will be recorded. In addition, hand grip strength measurement, pulmonary function test, and modified frailty index (a scoring system that includes 11 parameters) will be recorded prior to surgery. Intraoperative and postoperative complications will be documented. The duration of the patient's stay in the intensive care unit, chest tube removal, length of hospital stay, and postoperative complications will also be recorded. A follow-up call will be made to the patient by the responsible researcher 90 days after the operation to inquire about any complications that may have developed within that time frame.

The study aims to investigate the relationship between preoperative hand grip strength measurement, pulmonary function test analysis (PFT), and modified frailty index with the duration of intensive care unit stay, chest tube withdrawal time, hospital stay, and postoperative complications in patients undergoing lung resection due to malignancy.

Enrollment

100 estimated patients

Sex

All

Ages

40+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • All patients over the age of 40 who will undergo lung resection due to malignancy

Exclusion criteria

  • Patients undergoing emergency surgery
  • Patients with missing preoperative measurements
  • Patients with missing 90-day follow-up data

Trial design

100 participants in 2 patient groups

Complications (No)
Description:
Patients who did not experience any postoperative complications within 90 days.
Treatment:
Device: Hand Dynamometer
Other: Modified Frailty Index
Diagnostic Test: Pulmonary Function Test
Complications (Yes)
Description:
Patients who experienced any complications within 90 days after surgery.
Treatment:
Device: Hand Dynamometer
Other: Modified Frailty Index
Diagnostic Test: Pulmonary Function Test

Trial contacts and locations

1

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Central trial contact

Gülay ÜLGER, specialist

Data sourced from clinicaltrials.gov

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