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Effect of a Repeated Verbal Reminder of Orientation on Emergence Agitation After General Anesthesia

Status: Recruiting
Location: See location...
Intervention Type: Other
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

The Study will be conducted at SKMCH \& RC Lahore. All adult patients aged 18-70 years scheduled to undergo elective laparoscopic abdominal surgery will be screened for eligibility according to inclusion \& exclusion criteria. Total number of patients is 42. Patients who meet eligibility criteria will be randomized into 2 groups, Orientation group \& Control group. In orientation group, orientation reminder will be given in the form of prerecorded voice notes via headphones to the patients. The evaluation of emergence agitation will be done by using Riker Sedation Agitation Scale. The primary outcome will be incidence of emergence agitation in the OR. Secondary outcome includes the time from sevoflurane discontinuation to eye opening, extubation, discharge to PACU as well as pain score and length of stay in the PACU.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 70
Healthy Volunteers: f
View:

⁃ Adult patients

• Aged 18 to 70 years

• Scheduled to undergo elective laparoscopic abdominal surgery will be screened for eligibility.

Locations
Other Locations
Pakistan
Skmch & Rc
RECRUITING
Lahore
Contact Information
Primary
Muhammad Imran, Post graduation resident
imranhaider@skm.org.pk
0304-3662943
Backup
Dr. Saad ur Rehman, Consultant
saadurrehman@skm.org.pk
0343-4545963
Time Frame
Start Date: 2025-01-29
Estimated Completion Date: 2026-10-30
Participants
Target number of participants: 62
Treatments
Other: 3 including their name, the hospital name, and instructions to open their eyes , your operation has
Orientation group
Other: Patients in the control group will not receive any additional verbal stimulation during emergence ap
Control group
Related Therapeutic Areas
Sponsors
Leads: Shaukat Khanum Memorial Cancer Hospital & Research Centre

This content was sourced from clinicaltrials.gov