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Pregabalin in the Prevention of Postoperative Delirium and Pain

Primary Purpose

Delirium, Pain

Status
Completed
Phase
Phase 3
Locations
Canada
Study Type
Interventional
Intervention
Pregabalin
Sugar pill
Sponsored by
Ottawa Hospital Research Institute
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Delirium focused on measuring Postoperative, Perioperative, Orthopedic surgery, Vascular surgery, Gabapentinoid

Eligibility Criteria

60 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • aged 60 years and older
  • booked for major orthopaedic or vascular procedure
  • expected length of stay > 2 days

Exclusion Criteria:

  • open AAA repair
  • EVAR
  • allergy/sensitivity to pregabalin or gabapentin
  • use of pregabalin or gabapentin in previous 14 days
  • severe liver disease
  • severe renal dysfunction defined as either having creatinine clearance < 30 ml/min or being dialysis-dependent
  • seizure disorder
  • MMSE < 24/30
  • inability to speak English or French

Sites / Locations

  • The Ottawa Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Placebo Comparator

Experimental

Arm Label

Sugar pill

Pregabalin

Arm Description

Single dose given 30-60 minutes preoperatively, then given every 8 hours for 3 days postoperatively

Single dose of 75 mg given 30-60 minutes preoperatively, then 50 mg every 8 hours for 3 days postoperatively if creatinine clearance > 60 ml/min OR 25 mg every 8 hours for 3 days postoperatively if creatinine clearance 30-60 ml/min

Outcomes

Primary Outcome Measures

Delirium (patient is either CAM-ICU positive or positive for delirium by chart review)

Secondary Outcome Measures

Interference with daily activities using BPI
Pain at rest using NRS
Pain with movement of the operative site using NRS
Narcotic analgesic requirements
Sedation using RSS
Narcotic-related adverse effects using ORSDS
Recovery using the QoR
Length of stay
Medical Outcome Study (MOS) sleep score

Full Information

First Posted
January 8, 2009
Last Updated
January 9, 2012
Sponsor
Ottawa Hospital Research Institute
Collaborators
Pfizer
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1. Study Identification

Unique Protocol Identification Number
NCT00819988
Brief Title
Pregabalin in the Prevention of Postoperative Delirium and Pain
Official Title
A Randomized, Double-blind, Placebo-controlled Trial to Assess the Safety and Efficacy of the Perioperative Administration of Pregabalin in Reducing the Incidence of Postoperative Delirium and Improving Acute Postoperative Pain Management
Study Type
Interventional

2. Study Status

Record Verification Date
January 2012
Overall Recruitment Status
Completed
Study Start Date
May 2009 (undefined)
Primary Completion Date
September 2011 (Actual)
Study Completion Date
October 2011 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Ottawa Hospital Research Institute
Collaborators
Pfizer

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The purpose of this study is to determine whether administration of pregabalin by mouth immediately preoperatively and three times daily for 3 days after surgery reduces the incidence of delirium postoperatively and improves overall pain control.
Detailed Description
Delirium is a common postoperative complication occurring in up to 73% of patients sometime during their hospital stay. Elderly patients undergoing major surgical procedures are at highest risk. While many risk factors for delirium are known, the specific pathophysiology of postoperative delirium remains unclear and is likely multifactorial. The most common inciting agents and events include metabolic causes, medications, blood loss, hypoxemia and pain. Pain and its management are intimately related to the likelihood of developing postoperative delirium. As a class, gabapentinoids, such as pregabalin, have proven to reduce postoperative pain and narcotic consumption and therefore may have a role to play in the prevention of postoperative delirium.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Delirium, Pain
Keywords
Postoperative, Perioperative, Orthopedic surgery, Vascular surgery, Gabapentinoid

7. Study Design

Primary Purpose
Prevention
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
240 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Sugar pill
Arm Type
Placebo Comparator
Arm Description
Single dose given 30-60 minutes preoperatively, then given every 8 hours for 3 days postoperatively
Arm Title
Pregabalin
Arm Type
Experimental
Arm Description
Single dose of 75 mg given 30-60 minutes preoperatively, then 50 mg every 8 hours for 3 days postoperatively if creatinine clearance > 60 ml/min OR 25 mg every 8 hours for 3 days postoperatively if creatinine clearance 30-60 ml/min
Intervention Type
Drug
Intervention Name(s)
Pregabalin
Other Intervention Name(s)
Lyrica
Intervention Description
Pregabalin capsule 75 mg given preoperatively, then eith 50 mg or 25 mg given every 8 hours for 3 days postoperatively based on renal function
Intervention Type
Other
Intervention Name(s)
Sugar pill
Intervention Description
Single dose given 30-60 minutes preoperatively, then given every 8 hours for 3 days postoperatively
Primary Outcome Measure Information:
Title
Delirium (patient is either CAM-ICU positive or positive for delirium by chart review)
Time Frame
postoperative day 1, 2, 3
Secondary Outcome Measure Information:
Title
Interference with daily activities using BPI
Time Frame
postoperative day 3
Title
Pain at rest using NRS
Time Frame
postoperative days 1, 2, 3
Title
Pain with movement of the operative site using NRS
Time Frame
postoperative days 1, 2, 3
Title
Narcotic analgesic requirements
Time Frame
postoperative days 0, 1, 2, 3
Title
Sedation using RSS
Time Frame
postoperative days 1, 2, 3
Title
Narcotic-related adverse effects using ORSDS
Time Frame
postoperative days 1, 2, 3
Title
Recovery using the QoR
Time Frame
postoperative day 3
Title
Length of stay
Time Frame
Discharge day
Title
Medical Outcome Study (MOS) sleep score
Time Frame
Postoperative day 3

10. Eligibility

Sex
All
Minimum Age & Unit of Time
60 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: aged 60 years and older booked for major orthopaedic or vascular procedure expected length of stay > 2 days Exclusion Criteria: open AAA repair EVAR allergy/sensitivity to pregabalin or gabapentin use of pregabalin or gabapentin in previous 14 days severe liver disease severe renal dysfunction defined as either having creatinine clearance < 30 ml/min or being dialysis-dependent seizure disorder MMSE < 24/30 inability to speak English or French
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Alan J Chaput, MD, MSc
Organizational Affiliation
The Ottawa Hospital
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Homer Yang, MD
Organizational Affiliation
The Ottawa Hospital
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Gregory L Bryson, MD, MSc
Organizational Affiliation
The Ottawa Hospital
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Holly Evans, MD
Organizational Affiliation
The Ottawa Hospital
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Paul Beaule, MD
Organizational Affiliation
The Ottawa Hospital
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Prasad Jetty, MD
Organizational Affiliation
The Ottawa Hospital
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Barbara Power, MD
Organizational Affiliation
The Ottawa Hospital
Official's Role
Study Director
Facility Information:
Facility Name
The Ottawa Hospital
City
Ottawa
State/Province
Ontario
ZIP/Postal Code
K1Y 4E9
Country
Canada

12. IPD Sharing Statement

Citations:
PubMed Identifier
2240918
Citation
Inouye SK, van Dyck CH, Alessi CA, Balkin S, Siegal AP, Horwitz RI. Clarifying confusion: the confusion assessment method. A new method for detection of delirium. Ann Intern Med. 1990 Dec 15;113(12):941-8. doi: 10.7326/0003-4819-113-12-941.
Results Reference
background
PubMed Identifier
15370579
Citation
Bitsch M, Foss N, Kristensen B, Kehlet H. Pathogenesis of and management strategies for postoperative delirium after hip fracture: a review. Acta Orthop Scand. 2004 Aug;75(4):378-89. doi: 10.1080/00016470410001123.
Results Reference
background
PubMed Identifier
12560416
Citation
Morrison RS, Magaziner J, Gilbert M, Koval KJ, McLaughlin MA, Orosz G, Strauss E, Siu AL. Relationship between pain and opioid analgesics on the development of delirium following hip fracture. J Gerontol A Biol Sci Med Sci. 2003 Jan;58(1):76-81. doi: 10.1093/gerona/58.1.m76.
Results Reference
background
PubMed Identifier
12817919
Citation
Bekker AY, Weeks EJ. Cognitive function after anaesthesia in the elderly. Best Pract Res Clin Anaesthesiol. 2003 Jun;17(2):259-72. doi: 10.1016/s1521-6896(03)00005-3.
Results Reference
background
PubMed Identifier
9539601
Citation
Lynch EP, Lazor MA, Gellis JE, Orav J, Goldman L, Marcantonio ER. The impact of postoperative pain on the development of postoperative delirium. Anesth Analg. 1998 Apr;86(4):781-5. doi: 10.1097/00000539-199804000-00019.
Results Reference
background
PubMed Identifier
16738290
Citation
Gilron I. Review article: the role of anticonvulsant drugs in postoperative pain management: a bench-to-bedside perspective. Can J Anaesth. 2006 Jun;53(6):562-71. doi: 10.1007/BF03021846.
Results Reference
background
PubMed Identifier
17505569
Citation
Peng PW, Wijeysundera DN, Li CC. Use of gabapentin for perioperative pain control -- a meta-analysis. Pain Res Manag. 2007 Summer;12(2):85-92. doi: 10.1155/2007/840572.
Results Reference
background
PubMed Identifier
16914695
Citation
Leung JM, Sands LP, Rico M, Petersen KL, Rowbotham MC, Dahl JB, Ames C, Chou D, Weinstein P. Pilot clinical trial of gabapentin to decrease postoperative delirium in older patients. Neurology. 2006 Oct 10;67(7):1251-3. doi: 10.1212/01.wnl.0000233831.87781.a9. Epub 2006 Aug 16.
Results Reference
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Pregabalin in the Prevention of Postoperative Delirium and Pain

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