Geneva, Aug. 6 -- International Clinical Trials Registry received information related to the study (NCT07737093) titled 'Acapella vs Flutter Devices for Improving Breathing and Lung Function After Lobectomy' on July 21.
Study Type: Interventional
Study Design:
Allocation: Randomized. Intervention model: Parallel Assignment. Primary purpose: Treatment. Masking: None (Open Label).
Primary Sponsor: Riphah International University
Condition:
Lobotomy Syndrome
Intervention:
Device: Acapella Device Therapy (Experimental Arm 1):
Recruitment Status: Recruiting
Phase: N/A
Date of First Enrollment: June 20, 2026
Target Sample Size: 28
Countries of Recruitment:
Pakistan
To know more, visit https://clinicaltrials.gov/study/NCT077370...