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The Application of Docozine Combined With Sufentanil for Awake Tracheal Intubation

Phase 4
Completed
Conditions
Awake Tracheal Intubation
Interventions
Drug: Docozine
Drug: Saline
Registration Number
NCT02673723
Lead Sponsor
The First Affiliated Hospital of Anhui Medical University
Brief Summary

Mortality associated with difficult airway in anesthesia is up to 30%. So, it is urgent to find a safe and effective method for intubation. Awake tracheal intubation which is used to retain spontaneous breathing is one of the important measures to ensure the safety of the patients with difficult airway in anesthesia.

Sufentanil is used to provide good analgesia and can effectively inhibit the reaction of awake tracheal intubation, however, the outstanding problem is serious respiratory depression after intravenous sufentanil injection. Few study showed that dezocine is a kappa opioid antagonist related to mild respiratory depression and can prevents sufentanil-induced cough during general anesthesia induction.It is necessary to carry out large-scale, multi-center, randomized, controlled clinical study to determine whether dezocine prevents sufentanil-induced respiratory depression and whether dezocine combined sufentanil is a safe and effective method for awake tracheal intubation.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
520
Inclusion Criteria
  1. Written informed consent;
  2. Selective surgery and general anesthesia patients;
  3. Age 18-65 yrs;
  4. Anesthesia Society of American (ASA) Scale I~II;
Exclusion Criteria
  1. Mallampatis Ⅲ-Ⅳ;
  2. Heat rate < 50 beats/minutes;
  3. II-III Atrioventricular block;
  4. Use of alpha agonist or antagonist within two weeks;
  5. Use of opioid within 24 hours;
  6. Serious heart, liver, kidney disease and cerebrovascular disease;
  7. Allergic to the trial drug and other anesthesia drug contraindication;
  8. Factors existed that affect language communication;
  9. Any respiratory disease;
  10. Unsuccessful intubation for 3 times or drop out during intubation.

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
DezocineDocozineDezocine(Dez A:0.05 mg/kg,Dez B:0.1 mg/kg and Dez C:0.15 mg/kg, diluted to 5 ml respectively) is given for 10 seconds after surface anesthesia
ControlledSalineThe same amount of saline is given for 10 seconds after surface anesthesia
Primary Outcome Measures
NameTimeMethod
Sedation assessmentanesthesia induction

Observer's assessment of alertness/sedation(OAA/S) scale is used to assess the depth of sedation during anesthesia induction

The variation of blood pressureanesthesia induction

The variation of blood pressure(mmHg) during anesthesia induction

The occurrence of cough responseanesthesia induction

The cough scale is used to assess cough response the during anesthesia induction

The variation of heart rateanesthesia induction

The variation of heart rate(bpm)during anesthesia induction

The variation of pulse oxygen saturationanesthesia induction

The variation of pulse oxygen saturation(%) during anesthesia induction

Secondary Outcome Measures
NameTimeMethod
The occurrence of cardiovascular eventsfrom beginning of the anesthesia to the time the patients discharge, up to 3rd day after the surgery

The incidence of hypertension, hypotension, tachycardia and bradycardia from beginning of the anesthesia to the time the patients discharge, up to 3rd day after the surgery is recorded

The occurrence of treatment-related adverse eventsfrom beginning of the anesthesia to the time the patients discharge, up to 3rd day after the surgery

The incidence of treatment-related adverse events as assessed by CTCAE v4.0

Trial Locations

Locations (4)

The second People's Hospital of Wuhu

🇨🇳

Wuhu, Anhui, China

Anqing Municipal Hospital

🇨🇳

Anqing, Anhui, China

Chaohu Affiliated Hospital of Anhui Medical University

🇨🇳

Chaohu, Anhui, China

Second Affiliated Hospital of Anhui Medical University

🇨🇳

Hefei, Anhui, China

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