Comparison of Various Measures for Anticipating Difficult Laryngoscopy (COMPAD-T)
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| ClinicalTrials.gov Identifier: NCT04711018 |
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Recruitment Status :
Completed
First Posted : January 15, 2021
Last Update Posted : January 15, 2021
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| Condition or disease | Intervention/treatment |
|---|---|
| Difficult Laryngoscopy | Diagnostic Test: Laryngoscopy |
Creating a regression model among selected bedside tests for predicting difficult laryngoscopy )defined as Grade III or IV view during laryngoscopy according to Cormack-Lehane classification) is the primary objective. Recruiting of 145 ASA I-II adult patients who would have an elective surgery under general anesthesia were planned.
Criteria for exclusion were: a history of craniofacial surgery or restriction of cervical mobility, edentulous patients, pregnant women, patients who did not have a proper mouth opening (< 3 cm), and those who might require awake intubation or rapid sequence induction, cancellation of the surgery or change in the anesthetic strategy.
The selected tests and clinical situations were:
The presence of retrognathia (reduced temporomandibular joint-incisor distance) Buck teeth Modified Mallampati test (MMT) in the sitting position without phonation. A scale ranging between 1 and 4 points is used and scores of 3 or 4 are considered as predictors of DL. Upper lip bite test (ULBT) performed in a neutral position. ULBT is graded as 1-3 according to the extension ability of lower incisors.
Sternomental distance - The distance between the mentum and upper border of the manubrium sterni when the head is fully extended and the mouth is closed.
Thyromental distance (TMD) - The distance between mentum and the thyroid notch when the head is fully extended.
Interincisor distance (IID) - The distance between upper and lower incisors when the mouth is fully opened.
Neck circumference (NC) - It was measured at the level of the cricoid cartilage, perpendicular to the cervical axis.
The patients are premedicated with 0.03 mg/kg and oxygenated with the help of a bag-mask. Anesthesia is induced by consequent administration of 2 mcg/kg fentanyl, 1 mg/kg lidocaine, 2 mg/kg propofol, and 0.7 mg/kg rocuronium bromide thereafter. Two minutes after induction, the laryngoscopy is performed
| Study Type : | Observational |
| Actual Enrollment : | 145 participants |
| Observational Model: | Case-Control |
| Time Perspective: | Cross-Sectional |
| Official Title: | Comparison of Various Measures for Anticipating Difficult Laryngoscopy in Turkish Population: An Observational Study |
| Actual Study Start Date : | February 1, 2020 |
| Actual Primary Completion Date : | March 31, 2020 |
| Actual Study Completion Date : | May 31, 2020 |
| Group/Cohort | Intervention/treatment |
|---|---|
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Group DL (+)
Grade III or IV laryngeal view according to Cormack-Lehane classification
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Diagnostic Test: Laryngoscopy
The laryngoscopy is performed with the help of an appropriate size Macintosh blade. The patient's head is held in the sniffing position. External manipulation is not used for improving the view in this investigation. |
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Group DL (-)
Grade I or II laryngeal view according to Cormack-Lehane classification
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Diagnostic Test: Laryngoscopy
The laryngoscopy is performed with the help of an appropriate size Macintosh blade. The patient's head is held in the sniffing position. External manipulation is not used for improving the view in this investigation. |
- Difficult laryngoscopy [ Time Frame: Up to two weeks after preoperative examination ]Grade III or IV laryngeal view before endotracheal intubation
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| Ages Eligible for Study: | 18 Years to 65 Years (Adult, Older Adult) |
| Sexes Eligible for Study: | All |
| Accepts Healthy Volunteers: | Yes |
| Sampling Method: | Probability Sample |
Inclusion Criteria:
- ASA I-II
- Candidate for elective surgery under general anesthesia
Exclusion Criteria:
- History of craniofacial surgery or restriction of cervical mobility,
- Edentulous patients
- Pregnancy
- Patients who do not have a proper mouth opening (< 3 cm)
- Patients who might require awake intubation or rapid sequence induction.
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): NCT04711018
| Turkey | |
| Avcılar Murat Koluk State Hospital | |
| Istanbul, Turkey, 34320 | |
Other Publications:
| Responsible Party: | Derya Ozden Omaygenc, M.D., Haseki Training and Research Hospital |
| ClinicalTrials.gov Identifier: | NCT04711018 |
| Other Study ID Numbers: |
HasekiTRERH |
| First Posted: | January 15, 2021 Key Record Dates |
| Last Update Posted: | January 15, 2021 |
| Last Verified: | January 2021 |
| Individual Participant Data (IPD) Sharing Statement: | |
| Plan to Share IPD: | No |
| Studies a U.S. FDA-regulated Drug Product: | No |
| Studies a U.S. FDA-regulated Device Product: | No |
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Cephalometry Endotracheal intubation Ethnicity Laryngoscopy |

