Actively Recruiting
Effect of a Repeated Verbal Reminder of Orientation on Emergence Agitation After General Anesthesia
Led by Shaukat Khanum Memorial Cancer Hospital & Research Centre · Updated on 2026-04-03
62
Participants Needed
1
Research Sites
13 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Researchers are evaluating the effect of repeated verbal orientation reminders on emergence agitation in adult patients aged 18 to 70 years undergoing elective laparoscopic abdominal surgery under general anesthesia. The study aims to compare patients receiving these repeated reminders with those receiving usual care to see if the reminders reduce the frequency of emergence agitation and improve recovery after surgery. The trial is being conducted at Shaukat Khanum Memorial Hospital in Lahore and is registered with a clinical trials registry. Participants will be randomly assigned to one of two groups: the orientation group, which receives prerecorded voice reminders through headphones during emergence from anesthesia, or the control group, which only hears their own names and instructions to open their eyes. Anesthesia is induced and maintained with standard medications including propofol, fentanyl, atracurium, and sevoflurane. The orientation reminders are played every five seconds starting when anesthesia depth decreases, continuing until eye opening. The control group receives no additional verbal stimulation. Participants will be assessed using the Riker Sedation Agitation Scale to evaluate emergence agitation every five minutes from anesthesia lightening until discharge from the operating room. Researchers will measure the incidence of emergence agitation as the primary outcome. Secondary outcomes include timing of eye opening, extubation, discharge to the post-anesthesia care unit (PACU), pain scores, and length of stay in PACU. Standard monitoring and assessments will be performed throughout, and the total study duration lasts until all patients are recruited and evaluated.
CONDITIONS
Brief Title
Effect of a Repeated Verbal Reminder of Orientation on Emergence Agitation After General Anesthesia
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Adult patients aged 18 to 70 years
- Scheduled to undergo elective laparoscopic abdominal surgery
You will not qualify if you...
- Use of total intravenous anesthesia or inhalational agents other than sevoflurane
- American Society of Anesthesiologists (ASA) physical status 4
- Body mass index (BMI) greater than 35 kg/m^2
- Pre-existing neurological deficits
- Documented cognitive impairment by neurologist
- Hearing disorders
- Use of antipsychotic medications
- Planned ambulatory surgery
- Participant refusal
AI-Screening
AI-Powered Screening
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Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - Surgery day and emergence period
Participants receive general anesthesia for elective laparoscopic abdominal surgery. The orientation group hears repeated verbal reminders via prerecorded voice notes during emergence, while the control group hears only their name and instructions to open their eyes.
1 visit (in-person, day of surgery)
Duration - Until discharge from PACU
Participants are monitored in the post-anesthesia care unit (PACU) for recovery outcomes including pain scores and length of stay.
1 visit (in-person, post-surgery recovery)
Trial Site Locations
Total: 1 location
1
Skmch & Rc
Lahore, Punjab Province, Pakistan, 042
Actively Recruiting
Research Team
M
Muhammad Imran, Post graduation resident
D
Dr. Saad ur Rehman, Consultant
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
PREVENTION
Number of Arms
2
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