Controlled-Release Oxycodone For Postoperative Analgesia After Video-Assisted Thoracic Surgery
Primary Purpose
Anesthesia Recovery Period, Pain, Postoperative
Status
Terminated
Phase
Phase 4
Locations
Italy
Study Type
Interventional
Intervention
Morphine
oxycodone
Paravertebral block
Propofol
Remifentanil
Paracetamol
Morphine
Sponsored by
About this trial
This is an interventional treatment trial for Anesthesia Recovery Period focused on measuring Care, Postoperative, Analgesia, Analgesics, Opioid, Morphine, Remifentanil, Oxycodone, Anesthesia, Regional, Anesthesia, Intravenous, Preanesthetic Medication, Analgesia, Patient-Controlled
Eligibility Criteria
Inclusion Criteria:
- Patients scheduled for video-assisted thoracic surgery for clinical diagnosis of spontaneous pneumothorax
- Must be able to swallow tablets 1 h before surgery
- American Society of Anesthesiologists (ASA) physical status class I or II
Exclusion Criteria:
- Known allergy or other contraindications to study drugs
- Acute myocardial infarction ≤6 months before enrollment
- Serum creatinine > 2 mg/dL
- Body mass index (BMI) > 30
- Diagnosis of psychiatric disorders
- Known or possible pregnancy
- Epilepsy
- Chronic opioid therapy or abuse
Sites / Locations
- University Hospital / Azienda Ospedaliero-Universitaria
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Experimental
Arm Label
Control
CROxy
Arm Description
Control intervention will be intraoperative i.v. morphine administration 30 minutes before the end of anesthesia.
The intervention group will receive controlled-release oxycodone 1 h pre-operatively
Outcomes
Primary Outcome Measures
Morphine consumption (intravenous titration in PACU + i.v. patient-controlled pump usage)
Secondary Outcome Measures
Pain intensity as measured on a visual analog scale
Time to discharge from post-anesthesia care unit (Aldrete score >9)
Nausea or vomiting
Respiratory depression (SpO2 < 92% or respiratory rate <8)
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT00681174
Brief Title
Controlled-Release Oxycodone For Postoperative Analgesia After Video-Assisted Thoracic Surgery
Official Title
Preoperative Controlled-Release Oxycodone or Intraoperative Morphine As Transition Opioid After Intravenous Anesthesia For Video-Assisted Thoracic Surgery: a Randomized, Double-blind, Controlled Trial.
Study Type
Interventional
2. Study Status
Record Verification Date
January 2012
Overall Recruitment Status
Terminated
Why Stopped
Failure to enroll sufficient patients by expected deadline.
Study Start Date
July 2008 (undefined)
Primary Completion Date
November 2010 (Actual)
Study Completion Date
November 2010 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Parma
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
The main hypothesis of this study is that preoperative administration of controlled-release (CR) oxycodone may reduce acute postoperative pain and improve time to discharge from the post-anesthesia care unit in patients undergoing video-assisted thoracoscopy for spontaneous pneumothorax.
The study drug will be compared with intravenous morphine administered 30 minutes before the end of anesthesia.
Detailed Description
Although spontaneous pneumothorax may be treated conservatively by simple observation or chest tube insertion, up to 50% of patients treated conservatively may experience recurrence in subsequent months or years.
Video-assisted thoracic surgery (VATS) is a minimally-invasive surgical approach to treat spontaneous pneumothorax and reduce the risk of recurrence. Compared to open thoracotomy, VATS may facilitate a faster recovery and lead to earlier home discharge.
Totally-intravenous anesthesia (TIVA) with propofol and remifentanil is a useful anesthetic technique for VATS, as the drugs are rapidly eliminated after the end of the procedure, leading to fast recovery from anesthesia.
One drawback of ultra-short-acting opioid remifentanil is residual hyperalgesia after the end of the infusion, particularly after VATS, which is associated with relatively short but intense pain after surgery.
Intravenous morphine, administered just before the end of anesthesia, is the typical choice for pain relief after TIVA. However, this drug may require repeated titration and may be associated with postoperative nausea and vomiting, itchiness or drowsiness in the early postoperative period.
Oxycodone, another opioid, is available in an oral controlled-release (CR) formulation which grants relatively constant plasma levels of the drug after 1 h of administration.
The investigators hypothesize that administration of CR oxycodone 20 mg 1 hour before surgery may lead to better recovery parameters in the post-anesthesia care unit, thus granting earlier discharge to the surgical ward.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Anesthesia Recovery Period, Pain, Postoperative
Keywords
Care, Postoperative, Analgesia, Analgesics, Opioid, Morphine, Remifentanil, Oxycodone, Anesthesia, Regional, Anesthesia, Intravenous, Preanesthetic Medication, Analgesia, Patient-Controlled
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderOutcomes Assessor
Allocation
Randomized
Enrollment
22 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Control
Arm Type
Active Comparator
Arm Description
Control intervention will be intraoperative i.v. morphine administration 30 minutes before the end of anesthesia.
Arm Title
CROxy
Arm Type
Experimental
Arm Description
The intervention group will receive controlled-release oxycodone 1 h pre-operatively
Intervention Type
Drug
Intervention Name(s)
Morphine
Intervention Description
0.15 mg/kg i.v. bolus, 30 minutes before the expected end of anesthesia
Intervention Type
Drug
Intervention Name(s)
oxycodone
Other Intervention Name(s)
controlled-release oxycodone, CR oxycodone, OxyContin®
Intervention Description
20 mg p.o. 1 h before the start of anesthesia
Intervention Type
Procedure
Intervention Name(s)
Paravertebral block
Other Intervention Name(s)
Paravertebral nerve block, Naropin®
Intervention Description
Three injections of 0.5% ropivacaine, 5 ml each
Injections at the T5, T6 and T7 levels
A 22G spinal needle will be used to contact the ipsilateral transverse process; the needle will be "walked off" the process and the injection will be made 1 cm deeper.
Intervention Type
Drug
Intervention Name(s)
Propofol
Other Intervention Name(s)
Propofol TCI, target-controlled infusion, TIVA, TCI-TIVA, TIVA-TCI, Diprivan®
Intervention Description
Plasma concentration target-controlled infusion based on bispectral index values
Acceptable range of concentrations: 2-4 µg/mL
Target bispectral index values: 40-60
Infusion starts at 4 µg/ml target, after pre-oxygenation (i.e., start of anesthesia)
Intervention Type
Drug
Intervention Name(s)
Remifentanil
Other Intervention Name(s)
TIVA, Ultiva®
Intervention Description
50 µg/mL i.v. solution infused at 0.05-0.2 µg/kg/min
Infusion starts 7 min before propofol infusion (i.e., start of anesthesia)
Infusion rate adjusted to maintain mean arterial blood pressure within ±20% of baseline values.
Infusion stopped after end of surgery and after patients are brought back to the supine position (i.e., end of anesthesia)
Intervention Type
Drug
Intervention Name(s)
Paracetamol
Other Intervention Name(s)
Acetaminophen, Perfalgan®
Intervention Description
1 g i.v. bolus 30 min before the end of anesthesia; 1 g i.v. bolus q8h thereafter.
Intervention Type
Drug
Intervention Name(s)
Morphine
Other Intervention Name(s)
PCA, IVPCA, IV-PCA, PCA-IV, Patient-controlled analgesia
Intervention Description
Patient-controlled intravenous infusion pump (IV-PCA).
50 mg morphine in 50 ml saline solution (1 mg/ml)
Incremental dose: 1 mg
Lock-out time: 8 min
Limit: 40 mg in 4 h
Background infusion: none
Primary Outcome Measure Information:
Title
Morphine consumption (intravenous titration in PACU + i.v. patient-controlled pump usage)
Time Frame
48 h
Secondary Outcome Measure Information:
Title
Pain intensity as measured on a visual analog scale
Time Frame
1 h after end of anesthesia
Title
Time to discharge from post-anesthesia care unit (Aldrete score >9)
Time Frame
0-12 h after end of anesthesia
Title
Nausea or vomiting
Time Frame
48 h
Title
Respiratory depression (SpO2 < 92% or respiratory rate <8)
Time Frame
48 h
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Patients scheduled for video-assisted thoracic surgery for clinical diagnosis of spontaneous pneumothorax
Must be able to swallow tablets 1 h before surgery
American Society of Anesthesiologists (ASA) physical status class I or II
Exclusion Criteria:
Known allergy or other contraindications to study drugs
Acute myocardial infarction ≤6 months before enrollment
Serum creatinine > 2 mg/dL
Body mass index (BMI) > 30
Diagnosis of psychiatric disorders
Known or possible pregnancy
Epilepsy
Chronic opioid therapy or abuse
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Guido Fanelli, MD
Organizational Affiliation
Section of Anesthesiology and Critical Care, Dept. of Anesthesiology, University of Parma, Italy
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Marco Berti, MD
Organizational Affiliation
II Unit of Anesthesia, Critical Care and Pain Medicine, University Hospital of Parma, Italy
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Franca Bridelli, MD
Organizational Affiliation
II Unit of Anesthesia, Critical Care and Pain Medicine, University Hospital of Parma, Italy
Official's Role
Principal Investigator
Facility Information:
Facility Name
University Hospital / Azienda Ospedaliero-Universitaria
City
Parma
State/Province
PR
ZIP/Postal Code
43100
Country
Italy
12. IPD Sharing Statement
Citations:
PubMed Identifier
14512683
Citation
Noppen M, Baumann MH. Pathogenesis and treatment of primary spontaneous pneumothorax: an overview. Respiration. 2003 Jul-Aug;70(4):431-8. doi: 10.1159/000072911.
Results Reference
background
PubMed Identifier
16223391
Citation
Hansen EG, Duedahl TH, Romsing J, Hilsted KL, Dahl JB. Intra-operative remifentanil might influence pain levels in the immediate post-operative period after major abdominal surgery. Acta Anaesthesiol Scand. 2005 Nov;49(10):1464-70. doi: 10.1111/j.1399-6576.2005.00861.x.
Results Reference
background
PubMed Identifier
8844441
Citation
Sunshine A, Olson NZ, Colon A, Rivera J, Kaiko RF, Fitzmartin RD, Reder RF, Goldenheim PD. Analgesic efficacy of controlled-release oxycodone in postoperative pain. J Clin Pharmacol. 1996 Jul;36(7):595-603. doi: 10.1002/j.1552-4604.1996.tb04223.x.
Results Reference
background
PubMed Identifier
16199417
Citation
Vogt A, Stieger DS, Theurillat C, Curatolo M. Single-injection thoracic paravertebral block for postoperative pain treatment after thoracoscopic surgery. Br J Anaesth. 2005 Dec;95(6):816-21. doi: 10.1093/bja/aei250. Epub 2005 Sep 30.
Results Reference
background
PubMed Identifier
17023279
Citation
Kaya FN, Turker G, Basagan-Mogol E, Goren S, Bayram S, Gebitekin C. Preoperative multiple-injection thoracic paravertebral blocks reduce postoperative pain and analgesic requirements after video-assisted thoracic surgery. J Cardiothorac Vasc Anesth. 2006 Oct;20(5):639-43. doi: 10.1053/j.jvca.2006.03.022. Epub 2006 Aug 8.
Results Reference
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Controlled-Release Oxycodone For Postoperative Analgesia After Video-Assisted Thoracic Surgery
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