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

Not yet recruiting

• Conditions: Complication,Postoperative; Lung Cancer
• Interventions: Device: Hand Dynamometer; Diagnostic Test: Pulmonary Function Test; Other: Modified Frailty Index

• Registration Number: NCT06338007
• Lead Sponsor: Atatürk Chest Diseases and Chest Surgery Training and Research Hospital

Brief Summary

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.

Detailed Description

Not available

Study Timeline

• Study First Submitted: 2024-03-24
• Study First Submitted QC: 2024-03-24
• Study First Posted: 2024-03-29
• Status Verified: 2024-04
• Last Update Submitted: 2024-04-16
• Last Update Posted: 2024-04-17
• Study Start: 2024-05-01
• Primary Completion: 2024-09-01
• Study Completion: 2025-01-01

Recruitment & Eligibility

• Status: NOT_YET_RECRUITING
• Sex: All
• Target Recruitment: 100

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

Study & Design

• Study Type: OBSERVATIONAL
• Study Design: Not specified

Arm && Interventions

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

Primary Outcome Measures

Name	Time	Method
Complication	90 days	Complication data for patients who underwent lung resection for malignancy during the 90-day follow-up period.

Trial Locations

Locations (1)

Ankara Atatürk Sanatorium Training and Research Hospital; 🇹🇷 Ankara, Keçiören, Turkey