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NCT07778953
90% Effective Infusion Time of Sufentanil to Prevent Induction Cough: A Biased Coin Sequential Study
Conditions: Cough
Sex: All
Ages: 18 Years – 99 Years
Healthy volunteers: No
Phase: NA
Enrollment: 120
Sponsor: Shiyou Wei
Location: Shaoyang University Affiliated First Hospital Shaoyang Hunan
Summary
This single-center, prospective biased coin up-and-down sequential study aims to determine the 90% effective infusion time (ET90) of sufentanil to prevent sufentanil-induced cough (SIC) during the induction phase of general anesthesia in adults undergoing endotracheal intubation. Two age cohorts are studied separately: younger adults (\
Eligibility Criteria
Inclusion Criteria:
* American Society of Anesthesiologists (ASA) physical status I-III
* Aged ≥18 ears old
* Scheduled for elective surgery requiring general anesthesia with tracheal intubation
Exclusion Criteria:
* Resting vital signs upon operating-room arrival: systolic blood pressure ≥160 mmHg, or diastolic blood pressure ≥100 mmHg, or heart rate ≥110 beats per minute.
* Anticipated difficult airway, requirement for rapid-sequence induction, or emergency surgery.
* Chronic cough, asthma, chronic obstructive pulmonary disease (COPD), bronchiectasis, active pulmonary disease, or upper respiratory tract infection within the preceding 2 weeks.
* Regular opioid use for more than 2 weeks within 6 months before surgery; or recent use of antitussive agents or other medications that may alter the cough reflex.
* Known history of allergy to study drug (sufentanil citrate).
* Pregnancy, lactation, psychiatric disorders, or individuals unable to communicate appropriately.
Source: ClinicalTrials.gov (NCT07778953). StuddyBuddy aggregates publicly available trial information.