- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02689128
Postoperative Nausea and Vomiting: to Estimate the Incidence and Risk Factors in a Tertiary Teaching Hospital
Postoperative Nausea and Vomiting: A Prospective Observational Study to Estimate the Incidence and Risk Factors Over One Year in a Tertiary Teaching Hospital
Postoperative nausea and vomiting (PONV) is a frequent complication of surgery and anesthesia.
The aim of this study is to estimate the incidence and the risk factors of PONV at Jordan University Hospital over one year period.
Study Overview
Status
Conditions
Detailed Description
Postoperative nausea and vomiting (PONV) is a frequent complication of surgery and anesthesia, in the literature it reaches up to 70% of the surgical patients and it occurs after local and general anesthesia with surgery.
Locally in Jordan there was no proper clinical study to estimate PONV among surgical patients, the aim of this study is to estimate the incidence and the risk factors of PONV at Jordan University Hospital over one year period.
Study Type
Enrollment (Anticipated)
Contacts and Locations
Study Locations
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Amman, Jordan, 11942
- Recruiting
- University of Jordan
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Contact:
- Amira T Masri, Professor
- Phone Number: 2767 00962 6 5353444
- Email: amasri@ju.edu.jo
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Sub-Investigator:
- Salameh S Obeidat, M.B.B.S
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
- Patients who undergoes anesthesia and surgery.
- Patients who suffer from postoperative nausea and vomiting for 24 hours.
Exclusion Criteria:
- Patients who suffer from postoperative nausea and vomiting after 24 hours.
- Patients who undergoes Day-case surgery.
Study Plan
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
Postoperative nausea and vomiting
Time Frame: 24 hours
|
24 hours
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Collaborators and Investigators
Sponsor
Investigators
- Study Chair: Subhi M Alghanem, FFARCS, University of Jordan
Publications and helpful links
Study record dates
Study Major Dates
Study Start
Primary Completion (Anticipated)
Study Completion (Anticipated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Estimate)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 269/14a/tk
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
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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