CompletedNot Applicable

Use of Subanesthetic Dose Propofol Before Extubation

Turkey (Türkiye)80 participantsStarted 2024-06-01

Plain-language summary

This study investigates whether administering a low, sub-anesthetic dose of propofol before extubation can reduce emergence agitation and improve perioperative comfort in patients undergoing rhinoplasty. Emergence agitation refers to restlessness and confusion during early recovery from anesthesia, which may affect patient safety and surgical conditions. The study evaluates agitation levels, recovery characteristics, and patient-reported comfort following propofol administration compared with standard care.

Who can participate

Age range18 Years – 65 Years

SexALL

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * Ages 18-65 years * Patients scheduled for rhinoplasty surgery * ASA physical status I-II * No respiratory tract infection * Provided written informed consent Exclusion Criteria: * Refusal to participate * Presence of any respiratory tract infection * Younger than 18 or older than 65 * ASA III-IV * Known allergy to study medications * Predicted difficult intubation

What they're measuring

Changing Preoperative Anxiety Score (STAI)

Timeframe: 15 minutes (T1-T2)

Trial details

NCT IDNCT07276633

SponsorYuzuncu Yil University

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2024-09-01

View on ClinicalTrials.gov More Emergence Agitation trials