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A Study of sevoflurane combined with modified SAYGO technique in difficult airway intubation of burn patients.

A Study of sevoflurane combined with modified SAYGO technique in difficult airway intubation of burn patients.

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000034568
Enrollment
Unknown
Registered
2020-07-10
Start date
2018-06-01
Completion date
Unknown
Last updated
2020-07-13

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

Conditions

burn patients with difficult airway

Interventions

one:DEX + traditional surface anesthesia
two:DEX + modified SAYGO techology
three:SEV+ modified SAYGO techology

Sponsors

Department of Anesthesia, Southwest Hospital, Army Military Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: (1) Aged 18-70 years old; (2) ASA I-II was evaluated before operation; (3) Scar formation after head and neck burn; (4) Pharyngeal structure: improved Mallampati grade III-IV; (5) Opening degree: the distance between the upper and lower incisors when the maximum opening is less than 3cm, or less than the two transverse fingers of the examiner; (6) The distance between the nail and chin is the distance from the upper edge of the nail cartilage notch to the tip of the mandible when the head is in the fully extended position. The distance between the nail and chin is less than 6cm or less than the width of the three transverse fingers of the examiner; (7) Temporomandibular joint mobility: the patient could not make the upper and lower incisors aligned or the lower lip could not bite the upper lip completely; (8) Head and neck mobility: chin can't touch sternum or extend neck; (9) Volunteer to participate in the study and sign informed consent. Meeting above (1) (2) (3) (9) and any one of (4) (8) can be included in the study.

Exclusion criteria

Exclusion criteria: (1) Patients with heart disease and hypertension; (2) Patients with respiratory insufficiency, pulmonary infection and COPD; (3) Patients with severe internal organ injury; (4) The researchers think other reasons are not suitable for clinical researchers.

Design outcomes

Primary

MeasureTime frame
Hemodynamics and oxygenation parameters;Endotracheal intubation;Use of local anesthetics;Main outcome measures;

Secondary

MeasureTime frame
Postoperative complications;Whether the patient has memory during tracheal intubation.;The satisfaction degree of patients with tracheal intubation after operation.;

Countries

China

Contacts

Public ContactKaizhi Lu

Department of Anesthesia, Southwest Hospital, Army Military Medical University

lukaizhi2010@163.com+86 023 68754197

Outcome results

None listed

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