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The Effects of Bimanual Laryngoscopy on Post-Operative Sore Throat in Adults

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ClinicalTrials.gov Identifier: NCT01459354
Recruitment Status : Unknown
Verified October 2011 by China Medical University Hospital.
Recruitment status was:  Recruiting
First Posted : October 25, 2011
Last Update Posted : October 25, 2011
Sponsor:
Information provided by (Responsible Party):

Study Description
Brief Summary:
Post-operative sore throat, cough, and hoarseness of voice are common, uncomfortable, distressing sequelae after tracheal intubation. It was postulated that these effects are because of irritation and inflammation of the airway. Bimanual laryngoscopy is known to improve visual field during intubation. This procedure might reduce laryngeal trauma during intubation and therefore reduce the incidence or degree of post-operative sore throat. This is the first prospective, double-blinded, controlled study, which is focused on the effects of bimanual laryngoscopy on first 24-houred post-operative sore throat (POST).

Condition or disease
Postoperative Sorethroat Bimanual Laryngoscopy

Study Design

Study Type : Observational
Estimated Enrollment : 490 participants
Observational Model: Case Control
Time Perspective: Prospective
Study Start Date : August 2011

Resource links provided by the National Library of Medicine

MedlinePlus related topics: Sore Throat
U.S. FDA Resources

Groups and Cohorts

Group/Cohort
post, bimanual laryngoscopy, POGO score
one control, one study group


Outcome Measures

Eligibility Criteria

Information from the National Library of Medicine

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Ages Eligible for Study:   20 Years to 70 Years   (Adult, Senior)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Sampling Method:   Probability Sample
Study Population
20-70 yrs patient receive elective surgery with general anesthesia without position change or any influence on sorethroat
Criteria

Inclusion Criteria:

  1. ASA I or II
  2. 20-70 y/o
  3. GAET for A. Breast op B. GYN op C. Upper/lower extremities op D. Ophthalmology op E. GU op F. minor surgery

Exclusion Criteria:

  1. emergency surgery
  2. head and neck surgery
  3. recent URI symptom in last one weeks with medication
  4. post op PCA use
  5. on NG/OG
  6. perioperative bucking
Contacts and Locations

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01459354


Contacts
Contact: Chen Kuen Bao, master 886-4-22052121-1925 or 1926 u702115@hotmail.com

Locations
Taiwan
China Medical University Hospital Recruiting
Taichung, taiwan ROC, Taiwan, 40447
Contact: Chen kuen bao, master    886-4-22052121-1925 or 1926    u702115@hotmail.com   
Sponsors and Collaborators
China Medical University Hospital
More Information

Responsible Party: China Medical University Hospital
ClinicalTrials.gov Identifier: NCT01459354     History of Changes
Other Study ID Numbers: DMR100-IRB-146
First Posted: October 25, 2011    Key Record Dates
Last Update Posted: October 25, 2011
Last Verified: October 2011

Additional relevant MeSH terms:
Pharyngitis
Pharyngeal Diseases
Stomatognathic Diseases
Respiratory Tract Infections
Respiratory Tract Diseases
Otorhinolaryngologic Diseases