Actively Recruiting
Differences in Speed of Recovery From Anesthesia for Intraoral Surgery
Led by Clinical Hospital Centre Zagreb · Updated on 2025-12-24
42
Participants Needed
1
Research Sites
116 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
The goal of this clinical trial is to compare two groups of patients going in general anesthesia for intraoral surgery, the first group TIVA with propofol and the second group inhalational with sevoflurane. The main questions it aims to answer are to asses speed and quality of recovery from general anesthesia. Participants will fill out a questionnaire to evaluate the quality of recovery from anesthesia using the QoR-40 1h, 24h, and 30 days after waking up from anesthesia in comparison to the results of the same questionnaire before surgery. Also, the investigators will perform a hand grip and bite strength test on the patients after waking up from anesthesia in the operating room, after 1 hour in the recovery room, and after 24 hours compared to preoperative values. The investigators will compare TIVA and Volatile groups to see if there are any differences in recovery seed, muscle strength recovery, postoperative nausea and vomiting, and shivering between groups.
CONDITIONS
Official Title
Differences in Speed of Recovery From Anesthesia for Intraoral Surgery
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patients older than 18 years
- ASA status 1-2
- Indicated for intraoral surgical procedure longer than 30 minutes
- Surgical interventions on soft tissues of the mouth, intraoral tumor excisions via transoral route
- Patients who agreed to participate and signed consent
You will not qualify if you...
- ASA status 3 or higher
- Need for postoperative ICU care
- Surgery lasting more than 2 hours
- Procedures involving injury to masticatory muscles or bone affecting bite strength
- Bone surgeries where bite force testing could cause injury
- Diseases of neuromuscular junction or muscle diseases such as myopathy or dystrophy
- Use of medications causing myopathy or muscle weakness
- Known allergies to study drugs
- Refusal to participate
AI-Screening
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Trial Site Locations
Total: 1 location
1
University Hospital Centre Zagreb
Zagreb, Croatia, 10000
Actively Recruiting
Research Team
I
Ivan Šitum, MD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
TRIPLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
SUPPORTIVE_CARE
Number of Arms
2
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