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Preemptive Analgesia With OxyContin Versus Placebo Before Surgery for Long Bone Fractures

Primary Purpose

Fractures

Status
Completed
Phase
Phase 4
Locations
Israel
Study Type
Interventional
Intervention
Oxycodone hydrochloride
Sponsored by
Rambam Health Care Campus
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Fractures focused on measuring long bone fracture, open fractures, closed fractures, trauma

Eligibility Criteria

18 Years - 60 Years (Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Patient consent. Age 18 years to 60 years. Isolated limb bone fracture/s. Exclusion Criteria: Patient refusal. Age 61 years and older. Known allergy to study medication. Multiple bone fractures in different limbs. Multiple trauma. Oncological patients. Respiratory depression / respiratory insufficiency / hypercarbia. Acute bronchial asthma. CNS depression / hallucinations. Alzheimer / dementia. Known convulsive disorder. Prostate hypertrophy. Paralytic ileus. Renal dysfunction (plasma creatinine > 1.5). Liver dysfunction. Adrenocortical insufficiency. Hypothyroidism. Pancreatitis. Pregnancy and lactating. Drug abuse, current or in the past. Alcohol abuse on admission to operating room.

Sites / Locations

  • RAMBAM Health Care Campus

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Placebo Comparator

Arm Label

study group

placebo group

Arm Description

pre operative medication with 20 mg oxycontine PO

pre operative medication with placebo tablet PO

Outcomes

Primary Outcome Measures

post operative pain scores during first 24 hours (Visual analog scale)

Secondary Outcome Measures

Time to first analgesic request
Total other pain medications at first 24 hours post operative
Time to first oral intake
Length of hospitalization

Full Information

First Posted
November 15, 2005
Last Updated
February 4, 2015
Sponsor
Rambam Health Care Campus
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1. Study Identification

Unique Protocol Identification Number
NCT00254631
Brief Title
Preemptive Analgesia With OxyContin Versus Placebo Before Surgery for Long Bone Fractures
Official Title
Preemptive Analgesia With OxyContin Versus Placebo Before Surgery for Long Bone Fractures
Study Type
Interventional

2. Study Status

Record Verification Date
February 2015
Overall Recruitment Status
Completed
Study Start Date
April 2007 (undefined)
Primary Completion Date
December 2008 (Actual)
Study Completion Date
December 2008 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Rambam Health Care Campus

4. Oversight

5. Study Description

Brief Summary
We would like to check whether pre-operative administration of an oral controlled-release opioid formulation (Oxycodone hydrochloride (OxyContin)) could result in a clear effect of preemptive analgesia.
Detailed Description
Preemptive analgesia is based on the concept of treating pain before inflicting the painful stimulus. One suggested mechanism is that transmission of pain signals is altered when the patient is treated before infliction of noxious stimulation. That prevents changes from happening in the nervous system, making transformation from acute to chronic pain ("central sensitization") less likely, and thus reducing post operative pain. Clinically, good post operative pain control has been shown to be an effective method for hastening patient convalescence and discharge. It makes part of a general approach aiming to accelerate surgical recovery through earlier enteric feeding and ambulation OxyContin tablets deliver Oxycodone at a controlled release manner, over 12 hours. After oral administration oral bioavailability is 60-87%. A biphasic absorption pattern is observed, describing the initial (0.6 hours) and prolonged (6.9 hours) release of Oxycodone from the OxyContin tablets. Clinical analgesia is observed within 1 hour of administration. We believe that this mode of oral drug release is more appropriate for the perioperative pain treatment of patients undergoing short to medium term operations: with timely administration, the first absorbed part of the drug reaches the plasma before infliction of the noxious stimuli, possibly counteracting primary sensitization, and the second part absorbed, acts on post operative ongoing pain, possibly counteracting more advanced stages of neuronal plasticity. Study Hypothesis: Our hypothesis is that post operative pain will be lowered by pre-operative administration of OxyContin. When comparing the two groups we will look for differences in observed parameters, especially VAS numbers, time to first analgesic request, post operative analgesic requirements, time to first oral intake and length of hospitalization, to confirm or deny our hypothesis.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Fractures
Keywords
long bone fracture, open fractures, closed fractures, trauma

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigator
Allocation
Randomized
Enrollment
65 (Actual)

8. Arms, Groups, and Interventions

Arm Title
study group
Arm Type
Active Comparator
Arm Description
pre operative medication with 20 mg oxycontine PO
Arm Title
placebo group
Arm Type
Placebo Comparator
Arm Description
pre operative medication with placebo tablet PO
Intervention Type
Drug
Intervention Name(s)
Oxycodone hydrochloride
Primary Outcome Measure Information:
Title
post operative pain scores during first 24 hours (Visual analog scale)
Time Frame
24 hours after surgery
Secondary Outcome Measure Information:
Title
Time to first analgesic request
Time Frame
at PACU
Title
Total other pain medications at first 24 hours post operative
Time Frame
first 24 hours after surgery
Title
Time to first oral intake
Time Frame
first 24 hours after surgery
Title
Length of hospitalization
Time Frame
after surgery

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
60 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patient consent. Age 18 years to 60 years. Isolated limb bone fracture/s. Exclusion Criteria: Patient refusal. Age 61 years and older. Known allergy to study medication. Multiple bone fractures in different limbs. Multiple trauma. Oncological patients. Respiratory depression / respiratory insufficiency / hypercarbia. Acute bronchial asthma. CNS depression / hallucinations. Alzheimer / dementia. Known convulsive disorder. Prostate hypertrophy. Paralytic ileus. Renal dysfunction (plasma creatinine > 1.5). Liver dysfunction. Adrenocortical insufficiency. Hypothyroidism. Pancreatitis. Pregnancy and lactating. Drug abuse, current or in the past. Alcohol abuse on admission to operating room.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Ruth Edery, MD
Organizational Affiliation
Rambam Health Care Campus
Official's Role
Principal Investigator
Facility Information:
Facility Name
RAMBAM Health Care Campus
City
Haifa
ZIP/Postal Code
31096
Country
Israel

12. IPD Sharing Statement

Citations:
PubMed Identifier
3419837
Citation
Bach S, Noreng MF, Tjellden NU. Phantom limb pain in amputees during the first 12 months following limb amputation, after preoperative lumbar epidural blockade. Pain. 1988 Jun;33(3):297-301. doi: 10.1016/0304-3959(88)90288-6.
Results Reference
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PubMed Identifier
8131242
Citation
Code WE, Yip RW, Rooney ME, Browne PM, Hertz T. Preoperative naproxen sodium reduces postoperative pain following arthroscopic knee surgery. Can J Anaesth. 1994 Feb;41(2):98-101. doi: 10.1007/BF03009799.
Results Reference
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PubMed Identifier
8346839
Citation
Woolf CJ, Chong MS. Preemptive analgesia--treating postoperative pain by preventing the establishment of central sensitization. Anesth Analg. 1993 Aug;77(2):362-79. doi: 10.1213/00000539-199377020-00026. No abstract available.
Results Reference
background
PubMed Identifier
10422923
Citation
Capdevila X, Barthelet Y, Biboulet P, Ryckwaert Y, Rubenovitch J, d'Athis F. Effects of perioperative analgesic technique on the surgical outcome and duration of rehabilitation after major knee surgery. Anesthesiology. 1999 Jul;91(1):8-15. doi: 10.1097/00000542-199907000-00006.
Results Reference
background
PubMed Identifier
15728066
Citation
Ong CK, Lirk P, Seymour RA, Jenkins BJ. The efficacy of preemptive analgesia for acute postoperative pain management: a meta-analysis. Anesth Analg. 2005 Mar;100(3):757-773. doi: 10.1213/01.ANE.0000144428.98767.0E.
Results Reference
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Preemptive Analgesia With OxyContin Versus Placebo Before Surgery for Long Bone Fractures

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