Actively Recruiting

Phase Not Applicable
Age: 18Years - 70Years
All Genders
ID07510516

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

Age: 18Years - 70Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Adult patients aged 18 to 70 years
  • Scheduled to undergo elective laparoscopic abdominal surgery
Not Eligible

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

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Treatment

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)

Post-operative Follow-up

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

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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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