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

The recruitment status of this study is unknown because the information has not been verified recently.
Verified October 2011 by China Medical University Hospital.
Recruitment status was  Recruiting
Sponsor:
Information provided by (Responsible Party):
China Medical University Hospital
ClinicalTrials.gov Identifier:
NCT01459354
First received: October 23, 2011
Last updated: October 24, 2011
Last verified: October 2011
  Purpose

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
Postoperative Sorethroat
Bimanual Laryngoscopy

Study Type: Observational
Study Design: Observational Model: Case Control
Time Perspective: Prospective

Resource links provided by NLM:


Further study details as provided by China Medical University Hospital:

Estimated Enrollment: 490
Study Start Date: August 2011
Groups/Cohorts
post, bimanual laryngoscopy, POGO score
one control, one study group

  Eligibility

Ages Eligible for Study:   20 Years to 70 Years
Genders Eligible for Study:   Both
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
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its ClinicalTrials.gov identifier: 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

No publications provided

Responsible Party: China Medical University Hospital
ClinicalTrials.gov Identifier: NCT01459354     History of Changes
Other Study ID Numbers: DMR100-IRB-146
Study First Received: October 23, 2011
Last Updated: October 24, 2011
Health Authority: Taiwan: Department of Health

ClinicalTrials.gov processed this record on July 20, 2014