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Main
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Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register. |
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Register:
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ClinicalTrials.gov |
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Last refreshed on:
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21 July 2016 |
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Main ID: |
NCT02831140 |
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Date of registration:
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26/05/2016 |
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Prospective Registration:
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No |
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Primary sponsor: |
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Public title:
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The Fast Track Rehabilitation in Thoracic Surgery
FTR-TS |
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Scientific title:
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The Fast Track Rehabilitation in Thoracic Surgery - A Prospective Randomized Study |
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Date of first enrolment:
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January 2016 |
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Target sample size:
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100 |
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Recruitment status: |
Recruiting |
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URL:
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https://clinicaltrials.gov/show/NCT02831140 |
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Study type:
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Interventional |
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Study design:
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Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Prevention
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Phase:
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N/A
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Countries of recruitment
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Tunisia
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Contacts
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Name:
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Imed Frihka, Professor |
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Address:
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Telephone:
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Email:
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Affiliation:
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Cardiovascular and thoracic surgery department - Habib Bourguiba University Hospital |
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Name:
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Ahmed Ben Ayed, Resident |
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Address:
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Telephone:
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23935354 |
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Email:
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ahmed.benayed.tunisia@gmail.com |
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Affiliation:
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Key inclusion & exclusion criteria
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Inclusion Criteria:
- All patients who have lung surgery during the study period after their consents are
included.
Exclusion Criteria:
- Patients who have bad general state are unable to move or require a wake in the
resuscitation.
- The Patients with thoracic soft tissue surgery.
- patients having mediastinoscopy, surgery of the chest wall or mediastinum.
Age minimum:
18 Years
Age maximum:
80 Years
Gender:
Both
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Health Condition(s) or Problem(s) studied
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Thoracic Surgery
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Intervention(s)
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Behavioral: commun interventions
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Behavioral: Early exercises
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Behavioral: Removing urinary probe and all catheters.
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Behavioral: Early alimentation
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Primary Outcome(s)
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Postoperative Complications: Atelectasis or re-expansion failure or pneumonic infection
[Time Frame: within postoperative 30 days]
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Secondary Outcome(s)
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Surgery postoperative Complications : pulmonary embolism or cardiac arrhythmia or pleural empyema
[Time Frame: within postoperative 30 days]
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The Length of Hospital Stay
[Time Frame: within postoperative 30 days]
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Pain
[Time Frame: in 1st hour , 2nd hour , 3rd hour , 6th hour 24th hour , 48th hour at the postoperative , within postoperative 30 days]
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Thoracic surgery postoperative Complications
[Time Frame: within postoperative 30 days]
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Secondary ID(s)
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FTRCCVTSFAX
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Source(s) of Monetary Support
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Please refer to primary and secondary sponsors
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Results
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Results available:
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Date Posted:
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Date Completed:
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URL:
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