- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06329817
Incidence of Regurgitation in Patients Undergoing Intubation in Semi-fowler v/s Supine Position
September 17, 2024 updated by: DR.Talha Arshad, Pak Emirates Military Hospital
Incidence of Regurgitation in Patients Undergoing Intubation in Semi-fowler v/s Supine Position in a Tertiary Care Hospital
One of the most dreaded complication of general anaesthesia is aspiration of gastric contents after induction of general anaesthesia.Many endeavours and measures have been practiced to reduce the incidence of aspiration pneumonia.One such method is to intubate the patient in semi-fowler or supine posture.My study is aimed to find out safe and best position between these two after induction of general anaesthesia to prevent aspiration pneumonia.
Study Overview
Status
Recruiting
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Estimated)
100
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Dr. Talha Arshad, MBBS
- Phone Number: +923368734399
- Email: talhaarshad1004@gmail.com
Study Locations
-
-
Punjab
-
Rawalpindi, Punjab, Pakistan, 44000
- Recruiting
- PEMH
-
Contact:
- PEMH
- Phone Number: +923317055191
- Email: rabbiafatimasattar555@gmail.com
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Yes
Description
Inclusion Criteria:
- Adults 18-60 years of age
- Must be able to talk
Exclusion Criteria:
- patients less than 18 years of age or above 60,
- Pregnant women
- Handicapped individuals
- patients with intestinal obstruction
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Prevention
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Supine position
|
Preventing aspiration pneumonia in general anaesthesia in two different position supine v/s semi - Fowler
|
|
Experimental: Semi- fowler position
|
Preventing aspiration pneumonia in general anaesthesia in two different position supine v/s semi - Fowler
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Prevention of aspiration pneumonia
Time Frame: 06 months
|
To document incidence of regurgitation
|
06 months
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Study Director: IRB PEMH Rwp, CPSP
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
March 16, 2024
Primary Completion (Estimated)
November 15, 2024
Study Completion (Estimated)
September 1, 2025
Study Registration Dates
First Submitted
March 16, 2024
First Submitted That Met QC Criteria
March 21, 2024
First Posted (Actual)
March 26, 2024
Study Record Updates
Last Update Posted (Actual)
September 19, 2024
Last Update Submitted That Met QC Criteria
September 17, 2024
Last Verified
June 1, 2024
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- A/28/ER/532/23
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.