- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05193266
Gastroesophageal Reflux Disease (GERD) Among ICU Survivors
Gastroesophageal Reflux Disease and Its Health-related Quality of Life Among ICU Survivors
Study Overview
Status
Conditions
Detailed Description
During study period, all patients who survived at the time of ICU discharge will be considered as per inclusion and exclusion criteria. All eligible participants will be screened for the presence of GERD. If GERD present, participants will be followed for their symptoms after 6 week of the ICU discharge. Participant who did not having GERD at the time of ICU discharge will also be followed for the presence of GERD symptoms at 6 weeks after ICU discharge, if participant develop GERD symptoms then they will be followed up again for next 6 weeks. In participants who had GERD symptoms, HRQL score will be collected including 6-week follow up, after obtaining the informed written consent.
Demographic and clinical characteristics of all eligible participants will be collected on structured proforma. ICU prognostication scores, i.e., Acute Physiologic and Chronic Health Evaluation (APACHE) II score and Sequential Organ Dysfunction Assessment (SOFA) will be noted. All relevant and possible risk factors during ICU stay will also be collected. Participants with GERD, GERD-HRQL score will be collected, including 6-week follow-up.
At the time of ICU discharge, participant will be asked for the preference for the way of communication during follow-up with the option of pre-stamped envelope for postal with questionnaire. Participants will be handed over these envelopes with mention of pre-defined follow-up date for that particular patient. In case participant has plan for SGPGIMS visit for his/her pre-scheduled follow-up with any specialty, then data for present study will be collected in person.
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
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UP
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Lucknow, UP, India, 226014
- Department of Critical Care Medicine, Sanjay Gandhi Postgraduate Institute of Medical Sciences (SGPGIMS)
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- Adult patients (>18 years) who survived at the time of ICU discharge
Exclusion Criteria:
- ICU stay <96 hours
- At the time of ICU discharge GCS <15
- Presence of open abdomen (post surgery)
- Presence of feeding tube at the time of ICU discharge
- Presence of abdominal drain or PEG tube at the time of ICU discharge
- Presence of tracheostomy tube at the time of ICU discharge
- Patient who do not provide written consent
- Pregnancy
Study Plan
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Prevalence of Gatroesophageal reflux disease (GERD) among ICU survivors
Time Frame: 12 weeks after ICU discharge
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Percentage of ICU survivors among whom Gatroesophageal reflux disease (GERD) present
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12 weeks after ICU discharge
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Gatroesophageal reflux disease-Health-related quality of life score among GERD present patients
Time Frame: 12 weeks after ICU discharge
|
Gatroesophageal reflux disease-Health-related quality of life score will be measured two times (6 weeks apart).
The minimum score is 0 and maximum score is 50.
Higher score means worse outcome.
|
12 weeks after ICU discharge
|
Collaborators and Investigators
Investigators
- Principal Investigator: Mohan Gurjar, MD, PDCC, Sanjay Gandhi Postgraduate Institute of Medical Sciences (SGPGIMS)
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
- Digestive System Diseases
- Pathologic Processes
- Disease Attributes
- Gastrointestinal Diseases
- Stomach Diseases
- Gastroenteritis
- Intestinal Diseases
- Esophageal Motility Disorders
- Deglutition Disorders
- Esophageal Diseases
- Esophagitis
- Peptic Ulcer
- Duodenal Diseases
- Gastroesophageal Reflux
- Esophagitis, Peptic
- Critical Illness
Other Study ID Numbers
- 2021-265-DM-EXP-43
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.
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