Surgical Outcome at HFSUH (POC)

February 25, 2021 updated by: Badhaasaa, Haramaya Unversity

Postoperative Complication and Associated Factors Among Patients Operated at Hiwot Fana Specialized University Hospital, Ethiopia

the study was conducted on already intervened hospital patients with surgical management and their final outcome was followed from the chart of the patients.

Study Overview

Status

Completed

Conditions

Intervention / Treatment

Detailed Description

It was a prospective chart review of operated patient at Hiwot fana specialized hospital for different emergency as well elective surgeries. The study subjects signed informed written consent and their data collected anonymously. the follow up protocol was until discharge from hospital the longest date as 30 days.

Study Type

Observational

Enrollment (Actual)

352

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

  • Ethiopia
    • Harari NS
      • Harar, Harari NS, Ethiopia, 251
        • HFSUH

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

  • Child
  • Adult
  • Older Adult

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Sampling Method

Non-Probability Sample

Study Population

all patient admitted surgical ward and underwent surgical intervention

Description

Inclusion Criteria:

  • all operated patients at surgical ward

Exclusion Criteria:

  • patients operated at other facilities and transferred here. readmission within a month of discharge

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

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
post operative complications
Time Frame: 7 days
the outcome variable is adichotomous on with no complication and has complictions
7 days

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Haramaya Unversity

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)

August 1, 2019

Primary Completion (Actual)

January 31, 2020

Study Completion (Actual)

February 28, 2020

Study Registration Dates

First Submitted

February 24, 2021

First Submitted That Met QC Criteria

February 25, 2021

First Posted (Actual)

February 26, 2021

Study Record Updates

Last Update Posted (Actual)

February 26, 2021

Last Update Submitted That Met QC Criteria

February 25, 2021

Last Verified

February 1, 2021

More Information

Terms related to this study

Keywords

Other Study ID Numbers

  • HU,CHMS

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

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.

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