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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01763177
Other study ID # EC56-008-08-1-1
Secondary ID
Status Completed
Phase N/A
First received January 4, 2013
Last updated November 15, 2015
Start date January 2013
Est. completion date June 2015

Study information

Verified date November 2015
Source Prince of Songkla University
Contact n/a
Is FDA regulated No
Health authority Thailand: Ethical Committee
Study type Interventional

Clinical Trial Summary

Rationale: Delivery dry gas during anesthesia is associated with post-operative sore throat (POST). Oxygen nebulizer therapy increases humidity to the airway, especially post-extubation.

Objective: To investigate the effect and complications of oxygen nebulizer therapy on POST.


Recruitment information / eligibility

Status Completed
Enrollment 1036
Est. completion date June 2015
Est. primary completion date June 2015
Accepts healthy volunteers No
Gender Both
Age group 18 Years to 75 Years
Eligibility Inclusion Criteria:

- Age 18-75 years

- Pre-operative Hb >10 g% or Hct > 30%

- American Society of Anesthesiologist (ASA) class I-III

- Elective surgery

- General anesthesia with oroendotracheal tube using Macintosh laryngoscope

- Not exposed to intraoperative nitrous oxide

- Oxygen saturation at room air > 95% before induction and at arrival the PACU

Exclusion Criteria:

- Cases needing ICU admission immediately post-operative

- Conditioning requiring post-operative oxygen therapy e.g. heart disease, pregnancy, morbid obesity, cardiac and thoracic surgery

- Patients' conditioning affecting to complication of nebulizer oxygen therapy e.g. pulmonary disease, bleomycin treatment

- Patient's conditioning affecting POST assessment e.g. pre-operative using ventilator, recent upper respiratory tract infection (URI), recent lower respiratory tract infection and history of difficult airway

- Surgical conditioning affecting POST e.g. airway surgery, oral surgery, esophageal and neck surgery

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Outcomes Assessor), Primary Purpose: Prevention


Related Conditions & MeSH terms


Intervention

Other:
Oxygen
Oxygen mask 40% 8 LPM for 30 minutes

Locations

Country Name City State
Thailand Department of anesthesiology, Faculty of Medicine, Prince of Songkla University Hat Yai Songkhla

Sponsors (1)

Lead Sponsor Collaborator
Prince of Songkla University

Country where clinical trial is conducted

Thailand, 

References & Publications (1)

oxygen nebulizer AND sore throat

Outcome

Type Measure Description Time frame Safety issue
Primary The effect of oxygen nebulizer therapy on post-operative sore throat Assess POST using scoring system and discomfort by interview. Sore throat scoring system is divided into 4 scores 0 means no sore throat
means minimal sore throat (less severe than cold)
means moderate sore throat (similar to cold)
means severe sore throat (more severe than cold)
at post-anesthetic care unit and 24-h post-operative Yes
Secondary To evaluate the adverse events (pulmonary complications, wound infection, and mortality) of post-operative complications related to oxygen therapy 24-h post-op and 30-d mortality Yes
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