The Stress Response in Laparoscopic Colorectal Surgery and Its Role in the Development of the Enhanced Recovery Program.
NCT ID: NCT01128088
Last Updated: 2014-05-21
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
133 participants
OBSERVATIONAL
2010-03-31
2012-01-31
Brief Summary
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The investigators aim to recruit patients from outpatient clinic undergoing keyhole bowel surgery in one unit and randomize them to receive one of two different pain relief methods after the operation. Patients will follow the same care as standard patients but their pain relief will differ between two already well established modalities. They will also receive different intravenous fluids. Blood will also be drawn at various intervals immediately after the operation for future analysis. The trial will be funded by the MATTU and will run for approximately 18 months. This trial will enable us to establish the stress response in the four groups and correlate it to the patient's outcome with an aim to refining the enhanced recovery program.
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Detailed Description
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Conditions
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Study Design
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COHORT
PROSPECTIVE
Study Groups
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PCA and Volulyte
No interventions assigned to this group
PCA and Hartmann's
No interventions assigned to this group
Spinal and Volulyte
No interventions assigned to this group
Spinal and Hartmann's
No interventions assigned to this group
Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
* Conversion to a traditional open operation (removes the elements of keyhole surgery)
* Contraindication to spinal anaesthesia: abnormal clotting, skin infection over or near the back, presence of neurological disorders or anatomical abnormalities of the vertebral column. (For patient safety)
* Contraindication to the use of oesophageal Doppler: oesophageal disease, recent oesophageal surgery or upper airway surgery, moderate to severe aortic valve disease and any condition that causes bleeding problems. (For patient safety)
* Diagnosis of diabetes mellitus (will confound the stress response analysis)
* Treatment with exogenous steroids in the proceeding 3 months (will confound the stress response analysis)
18 Years
ALL
No
Sponsors
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University of Surrey
OTHER
Responsible Party
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Principal Investigators
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Tim Rockall, MBBS FRCS MD
Role: STUDY_DIRECTOR
Minimal Access Therapy Training Unit
Locations
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The Royal Surrey County Hospital
Guildford, Surrey, United Kingdom
Countries
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References
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Day AR, Smith RV, Scott MJ, Fawcett WJ, Rockall TA. Randomized clinical trial investigating the stress response from two different methods of analgesia after laparoscopic colorectal surgery. Br J Surg. 2015 Nov;102(12):1473-9. doi: 10.1002/bjs.9936. Epub 2015 Sep 23.
Other Identifiers
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SURGN0008
Identifier Type: -
Identifier Source: org_study_id
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