A Trial Evaluating the Efficacy and Safety of HSK3486 Injectable Emulsion in Subjects Undergoing Fiberoptic Bronchoscopy

Haisco Pharmaceutical Group

Status and phase

Completed

Phase 3

Conditions

Sedation or Anesthesia

Treatments

Drug: HSK3486

Drug: Propofol

Study type

Interventional

Funder types

Industry

Identifiers

NCT04111159

HSK3486-303

Details and patient eligibility

About

This is a Multi-Center, Randomized, Double-Blind, Propofol-Controlled Phase III Clinical Trial. Around 260 eligible subjects are planned to be enrolled and randomized in a 1:1 ratio to either the HSK3486 arm or propofol arm. The main objective is to evaluate the efficacy of HSK3486 vs. propofol for the induction of sedation/anesthesia in subjects undergoing fiberoptic bronchoscopy.

Enrollment

267 patients

Sex

All

Ages

18 to 80 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

1.Subjects receiving laryngeal mask airway-assisted diagnostic and/or therapeutic fiberoptic bronchoscopy; 2.Male or female, ASA I-III, ≥ 18 and < 80 years old; 3.Body mass index (BMI) ≥ 18 and ≤ 30 kg/m2; 4.Respiratory rate ≥ 10 and ≤ 24 bpm; SpO2 ≥ 93%; SBP ≥ 90 mmHg; DBP ≥ 55 mmHg; HR ≥ 50 and ≤ 100 bpm during screening and baseline periods; 5.Capable of understanding the procedure and method of this study, willing to sign an informed consent form and to complete this study in strict accordance with the study protocol.

Exclusion criteria

Patients with contraindications to deep sedation/general anesthesia or a history of past sedation/anesthesia accidents;
Patient known to be allergic to eggs, soy products, opioids and their antidotes, and propofol; patient having contraindications to propofol, opioids and their antidotes;
Patients who have undergone endotracheal intubation and/or mechanical ventilation prior to diagnostic or therapeutic bronchoscopy;
Medical history or evidence of any of the following prior to screening/at baseline, which may increase sedation/anesthesia risk:
1. History of cardiovascular diseases: uncontrolled hypertension [systolic blood pressure (SBP) ≥170 mmHg and/or diastolic blood pressure (DBP) ≥105 mmHg without treatment, or SBP > 160 mmHg and/or DBP >100 mmHg after antihypertensive treatment], aneurysm, severe arrhythmia, heart failure, Adams-stokes syndrome, New York Heart Association (NYHA) Class ≥ III, severe superior vena cava syndrome, pericardial effusion, acute myocardial ischemia, unstable angina, myocardial infarction within 6 months before screening, history of tachycardia/bradycardia requiring medical treatment, II-III degree atrioventricular block (excluding patients with pacemakers) or QTcF interval ≥ 450 ms [during screening only (corrected using Fredericia's formula1)];
2. History of respiratory diseases: severe chronic obstructive pulmonary disease, acute exacerbation of chronic obstructive pulmonary disease, severe airway stenosis, throat mass, history of tracheoesophageal fistula or airway tear, severe respiratory infection within 2 weeks prior to screening;
3. History of neurological and psychiatric disorders: craniocerebral injury, possible convulsions, intracranial hypertension, cerebral aneurysms, history of cerebrovascular accidents; schizophrenia, mania, insanity, long-term use of psychotropic drugs, and history of cognitive dysfunction;
4. History of gastrointestinal diseases: gastrointestinal retention, active hemorrhage, or history of gastroesophageal reflux or obstruction that may lead to aspiration;
5. History of uncontrolled clinically significant liver, kidney, blood system, nervous system or metabolic system diseases judged by the investigator to be probably unsuitable for involvement in the study;
6. History of alcohol abuse within 3 months prior to screening, abuse defined as average of > 2 units of alcohol per day (1 unit = 360 mL beer or 45 mL liquor with 40% alcohol or 150 mL wine);
7. History of drug abuse within 3 months prior to screening;
8. History of blood transfusion within 14 days prior to screening;
Patients with the following respiratory risks during screening/at baseline:
1. Acute asthma attack;
2. Sleep apnea syndrome;
3. History of malignant hyperthermia or family history;
4. History of failed tracheal intubation;
5. Difficult airway (modified Mallampati score ≥ III) as determined by the investigator;
Patient who received any of the following medications or treatments during screening/at baseline:
1. Received any investigational drug within 1 month prior to screening;
2. Received propofol, other sedatives/anesthetics, and/or opioid analgesics or compounds containing analgesics within 72 h prior to baseline;
Laboratory results meeting any of the following criteria during screening/at baseline, confirmed by re-examination:
1. WBC ≤ 3.0 × 10^9/L;
2. Platelets ≤ 80 × 10^9/L;
3. Hemoglobin ≤ 80 g/L;
4. Prothrombin time ≥ 1.5 × ULN;
5. Activated partial thromboplastin time (aPTT) ≥ 1.5 × ULN;
6. ALT and/or AST ≥ 3 × ULN;
7. Total bilirubin ≥ 1.5 × ULN;
8. Serum creatinine ≥ 1.5 × ULN.
Women who are pregnant or breastfeeding; women of child-bearing potential or men who are unwilling to use contraception during the trial; or subjects who are planning pregnancy within 3 month after the completion of the trial (including male subjects);
Subject judged by the investigator to have any other factors unsuitable for involvement in the study.