Skip to content

Comparison of incidence of sore throat after tracheal intubation by Macintosh laryngoscope and Glidescope

]ncidence of sore throat after tracheal intubation

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT201309193773N9
Enrollment
300
Registered
2014-01-31
Start date
2013-03-21
Completion date
Unknown
Last updated
2018-02-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Condition 1: Dysphonia. Condition 2: sore throat. Dysphonia,Hoarseness acute sore throat,pharyngeal

Interventions

Intervention 1: One group will be intubated by Macintosh laryngoscope.Intubation will be done by tube number 7 or 7.5. Cuff tube will be adjusted between 20-25 mmHg. Patients’ general anesthesia will
One group will be intubated by Macintosh laryngoscope.Intubation will be done by tube number 7 or 7.5. Cuff tube will be adjusted between 20-25 mmHg. Patients’ general anesthesia will be induced and m
The other group will be intubated by Glidescope. Intubation will be done by tube number 7 or 7.5. Cuff tube will be adjusted between 20-25 mmHg. Patients’ general anesthesia will be induced and mainta

Sponsors

Tehran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria:Adult patients aged between 15 and 60 yr;A.S.A physical status 1 or 2 ; All patients underwent a preoperative air way evaluation they had early air way ;Patients who were operated in the supine position ;The incidence of Intubation In the End of Surgery is low;Time of Surgery: 2-4 hours. Exclusion criteria:Patients who had clinical evidence of active pulmonary disease;Patients had the previous intubation(If presence previous Anatomical Injury);Patients had artificial denture;Patients had congenital and acquisitive deformity in face neck and mouth and air way;Patients scheduled for neck or thoracic surgery;There were pathological wastage in mouth and pharynx

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Incidence of sore throat. Timepoint: 1,6,24,48 hours after operation. Method of measurement: By interview and by a 3 step scale ( contained none, moderate and high).;Intensity of sore throat. Timepoint: 1,6,24,48 hours after operation. Method of measurement: By interview and by a 3 step scale ( contained none, moderate and high).

Secondary

MeasureTime frame
Incidence of hoarseness following intubation. Timepoint: 1,6,24,48 hours after ooperation. Method of measurement: By interview and by a 3 step scale ( contained none, moderate and high).;Incidence of dysphagia following intubation. Timepoint: 1,6,24,48 hours after ooperation. Method of measurement: By interview and by a 3 step scale ( contained none, moderate and high).

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr Shirin Habibi

Tehran University of Medical Sciences

shirin_habibi@yahoo.com+98 217831157

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026