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An alternative method for regional airway blocks

Dissociative conscious sedation an alternative to regional airway blocks

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT201012075333N1
Enrollment
30
Registered
2011-08-29
Start date
2009-12-01
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

difficult laryngoscopy and difficult intubation. Complications of medical and surgical care

Interventions

1-Subcutaneous Ketamine 0.7mg/kg 2- intravenous Fentanyl 2-4 ug/kg 3- Anesthesia of the tongue, larynx and pharynx with lidocain spray 4%.
Prevention
1-Subcutaneous Ketamine 0.7mg/kg 2- intravenous Fentanyl 2-4 ug/kg 3- Anesthesia of the tongue, larynx and pharynx with lidocain spray 4%

Sponsors

Tehran university of Medical Scioences
Lead Sponsor

Eligibility

Sex/Gender
Male
Age
40 Years to 65 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: predicted difficult airway because of laryngeal tumors with impossible airway regional blocks Exclusion criteria: history of Psychological disorders, coronary artery disease, uncontrolled hypertension, increased ICP, intracranial mass lesions, open eye injury

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Possibility of laryngoscopy. Timepoint: time of intubation. Method of measurement: successful or not successful.;Possibility of fiberoptic bronchoscopy. Timepoint: time of intubation. Method of measurement: successful or not successful.;Possibility of rigid bronchoscopy. Timepoint: no time point. Method of measurement: successful or not successful.;Possibility of Double lumen endobronchial intubation. Timepoint: Evaluation of possibility of endobronchial intubation. Method of measurement: possibility of procedure.

Secondary

MeasureTime frame
Hemodynamic changes. Timepoint: 3-4 times during the procedure. Method of measurement: increased heart rate and blood pressure.;Spo2. Timepoint: continuous. Method of measurement: Pulseoximetry.;Patient's cooperation. Timepoint: during the procedure. Method of measurement: Possibility of tube insertion.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMihan Jafari Javid

Tehran University of Medical Sciences

jafarija@sina.ac.irmihanjavid@yahoo.com+98 21 6119 2329

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Mar 28, 2026