Actively Recruiting
Incidence of Regurgitation in Patients Undergoing Intubation in Semi-fowler v/s Supine Position in a Tertiary Care Hospital
Led by Pak Emirates Military Hospital · Updated on 2024-09-19
100
Participants Needed
1
Research Sites
41 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
This research aims to compare two different body positions during intubation—semi-fowler and supine—to find the safest method to reduce the risk of aspiration pneumonia, a serious complication that can occur after general anesthesia. The study focuses on patients undergoing general anesthesia for procedures, including those with bilateral inguinal hernia. The investigation is designed as a randomized trial to determine which position better prevents the inhalation of stomach contents into the lungs. Participants will be randomly assigned to one of two groups: one group will be intubated in the supine position, and the other in the semi-fowler position. Both positions are being studied to assess their impact on the incidence of regurgitation during the induction of general anesthesia. The study will last for six months, during which data on aspiration pneumonia prevention will be collected and evaluated. During the study, researchers will monitor participants closely for signs of aspiration pneumonia and other complications. Evaluations will include clinical assessments related to the safety and effectiveness of intubation positions. The study will also collect information on participants' ability to communicate verbally before the procedure. Participants can expect to be involved from the time of anesthesia induction through follow-up during the six-month period to assess the primary outcome of aspiration pneumonia prevention.
CONDITIONS
Brief Title
Incidence of Regurgitation in Patients Undergoing Intubation in Semi-fowler v/s Supine Position
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Adults 18-60 years of age
- Must be able to talk
You will not qualify if you...
- Patients younger than 18 years or older than 60 years
- Pregnant women
- Handicapped individuals
- Patients with intestinal obstruction
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
Duration - One-time procedure during surgery
Participants undergo intubation in either the supine or semi-fowler position to prevent aspiration pneumonia during general anesthesia.
1 visit (in-person)
Duration - 6 months
Participants are monitored for prevention of aspiration pneumonia over a 6-month period after intubation.
Periodic follow-up visits
Trial Site Locations
Total: 1 location
1
PEMH
Rawalpindi, Punjab Province, Pakistan, 44000
Actively Recruiting
Research Team
D
Dr. Talha Arshad, MBBS
How is the study designed?
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
PREVENTION
Number of Arms
2
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