Actively Recruiting

Phase Not Applicable
Age: 18Years - 60Years
All Genders
Healthy Volunteers
ID06329817

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

Age: 18Years - 60Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Adults 18-60 years of age
  • Must be able to talk
Not Eligible

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

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

Treatment

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)

Follow-up

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

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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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