Anesthesia for Ambulatory Pediatric Surgery in Sub-Saharan Africa (SSA)

Anesthesia for Ambulatory Pediatric Surgery in Sub-Saharan Africa (SSA): a Pilot Study in Burkina Faso

Long surgical wait-times and limited hospital capacity are common obstacles to surgical care in many countries in sub-Saharan Africa (SSA). Ambulatory surgery might offer a solution to these problems. The aim is to study the introduction of ambulatory surgery in a pediatric hospital in SSA.

This is a cross-sectional descriptive study which took place over 6 months. It includes all the patients assigned to ambulatory surgery in the Pediatric University Hospital in Ouagadougou, Burkina Faso.

Study Overview

Status

Completed

Conditions

Study Type

Interventional

Enrollment (Actual)

103

Phase

  • Not Applicable

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

1 year to 15 years (CHILD)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • ASA 1 status
  • elective surgery with low potential for blood loss or severe pain, lasting less than 90 minutes
  • whose parents could be contacted by telephone and who could return to the hospital in less than 1 hour
  • Parents gave consent for the surgical procedure

Exclusion Criteria:

  • non operative patients

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

  • Allocation: NA
  • Interventional Model: SINGLE_GROUP
  • Masking: NONE

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
OTHER: children undergoing ambulatory surgery

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Failure of ambulatory surgery
Time Frame: 1day
number of patients that have been hospitalized (for whom ambulatory have been conversed to hospitalization)
1day

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Morbidity
Time Frame: 3 days
Number of patients that presented complications of anesthesia or surgery such as nausea, vomiting, drowsiness and fever.
3 days
Complication after discharge from hospital
Time Frame: 3 days
number of phone calls from parents of patients after ambulatory discharge
3 days

Collaborators and Investigators

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

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

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

June 1, 2014

Primary Completion (ACTUAL)

November 1, 2014

Study Registration Dates

First Submitted

April 13, 2016

First Submitted That Met QC Criteria

May 5, 2016

First Posted (ESTIMATE)

May 9, 2016

Study Record Updates

Last Update Posted (ESTIMATE)

May 9, 2016

Last Update Submitted That Met QC Criteria

May 5, 2016

Last Verified

May 1, 2016

More Information

Terms related to this study

Other Study ID Numbers

  • A1

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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