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Clinical Trials/CTRI/2024/03/063778
CTRI/2024/03/063778Not yet recruitingUnknown

A randomized control trial to compare the time taken to perform acceptable spirometry between two groups after providing procedural demonstrational video with routine instructions versus only routine instructions. - NI

one0 sites0 target enrollmentStarted: TBDLast updated:

Trial Snapshot

Phase
Unknown
Status
Not yet recruiting
Sponsor
one

Study Overview

Brief Summary

No summary available.

Study Design

Study Type
Interventional

Eligibility Criteria

Inclusion Criteria

  • All patients, aged more than 18 years who are referred for spirometry ( who are undergoing spirometry for the first time)

Exclusion Criteria

  • Patients with
  • Acute myocardial infarction within 1 week
  • Systemic hypotension or severe failure
  • Uncontrolled pulmonary hypertension
  • Acute corpulmonale
  • Clinically unstable pulmonary embolism
  • History of syncope related to forced expiration/cough
  • Cerebral aneurysm, Brain surgery within 4 week
  • , recent concussion with continuing symptoms, eye surgery within 1 week
  • Sinus surgery or middle ear surgery or infection within 1 week
  • Presence of pneumothorax, thoracic surgery within 4 week, abdominal surgery within 4 week
  • Late-term pregnancy
  • Active or suspected transmissible respiratory or systemic infection, including tuberculosis

Investigators

Sponsor
one

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