Hemodynamic Effects of Physiotherapy in the Early Postoperative Period

Lung Diseases Clinical Trial

Official title:

Hemodynamic Effects of Physiotherapy in the Early Postoperative Period

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT03726541
• Other study ID #: Hemodynamics_ physiotherapy
• Status: Completed
• Phase: N/A
• Start date: November 1, 2018
• Est. completion date: December 30, 2018

Study information

• Verified date: March 2019
• Source: Istanbul Medipol University Hospital
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Physiotherapy will be applied to the patients who undergo thoracotomy operation after 24 hours of intensive care stay. Physiotherapy program includes breathing exercises, incentive spirometer training, ambulation. Oxygen saturation, heart rate and blood pressure values will be recorded before and after the training session. Changes in the follow-up parameters will be discussed.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 72
• Est. completion date: December 30, 2018
• Est. primary completion date: December 30, 2018
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 75 Years

Eligibility

Inclusion Criteria

• Between 18-75 age

• Hemodynamically stable

• Being conscious

Exclusion Criteria:

• Excessive pain

• Neurological complications

• Posttraumatic and musculoskeletal problems to prevent exercise

• Do not want to be included in the study

• Fever above 38 degrees

Related Conditions & MeSH terms

• Lung Diseases
• Physiotherapy
• Postoperative

Intervention

Other:
• physiotherapy
Physiotherapy program includes breathing exercises, incisive spirometer study, grade ambulation. Oxygen saturation, heart rate and blood pressure values will be recorded before and after the session. Changes in the follow-up parameters will be discussed.

Locations

Country	Name	City	State
Turkey	Yedikule Chest Disease Hospital	Istanbul	Zeytinburnu

Sponsors (1)

Lead Sponsor	Collaborator
Istanbul Medipol University Hospital

Country where clinical trial is conducted

Turkey, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Change from baseline oxygen saturation	The hearth rate response will be measured before and after exercise training with pulse oximeter.	30 minutes
Primary	Change from baseline hearth rate response.	The hearth rate response will be measured before and after exercise training with intensive care ECG	30 minutes
Primary	Change from baseline systolic and diastolic blood pressure response.	Blood pressure will be measured before and after exercise training with monometer from the arm	30 minutes