Effect of Vibratory Expiratory Pressure on Pulmonary Function After Lung Resection Surgery

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

78 participants

Study Classification

INTERVENTIONAL

Study Start Date

2013-01-31

Study Completion Date

2013-09-30

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

Postoperative airway clearance and recovery of pulmonary function after lung resection is critical in patients undergoing pulmonary resection surgery. The investigators hypothesized that vibratory positive expiratory pressure using the Acapella device may improve pulmonary function recovery in patients undergoing video-assisted thoracoscopic lung resection surgery.

Related Clinical Trials

Explore similar clinical trials based on study characteristics and research focus.

Driving Pressure and Postoperative Pulmonary Complications

NCT02851238

One-Lung Ventilation Postoperative Respiratory Complications Driving Pressure

COMPLETED NA

Optimal Level of PEEP in Protective One-lung Ventilation

NCT03856918

Video-assisted Thoracic Surgery Postoperative Atelectasis Positive End-expiratory Pressure

COMPLETED NA

Ventilator-driven Alveolar Recruitment Maneuver

NCT04258202

Postoperative Atelectasis Ventilator Lung Atelectasis +1 more

COMPLETED NA

Optimal PEEP Level for Minimizing the Risk of Postoperative Atelectasis: A Retrospective Cohort Study Based on Lung Ultrasound Monitoring

NCT07211074

Postoperative Pulmonary Complications (PPCs) Postoperative Atelectasis Lung Ultrasound

RECRUITING

Driving Pressure-guided PEEP Titration in Robot-assisted Laparoscopic Surgeries

NCT04327193

Atelectasis, Postoperative Pulmonary

COMPLETED NA

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Pulmonary Resection Surgery

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

SINGLE

Participants

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

Acapella

use of the Acapella device postoperatively

Group Type EXPERIMENTAL

Acapella device

Intervention Type DEVICE

Control

Group Type NO_INTERVENTION

No interventions assigned to this group

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

Acapella device

Intervention Type DEVICE

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

* patients between 20 and 65 years old
* undergoing video-assisted thoracoscopic lung resection surgery for suspicious lung cancer
* admission to intensive care unit in extubate state
* with intravenous patient-controlled analgesia

Exclusion Criteria

* body mass index of less than 15 kg/m2 or more than 30 kg/m2
* history of respiratory tract infection within 3 months
* emergency surgery
* preoperative supplemental oxygen or ventilator care
* preoperative PaO2 of less than 70 mmHg or PaCO2 of more than 50 mmHg
* preoperative FEV1 of less than 30% of predicted value
* unconsciousness or neuromuscular disease

Minimum Eligible Age

20 Years

Maximum Eligible Age

65 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No