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Safety and Efficacy of Pre-emptive Tapentadol vs Pregabalin in Post Operative Pain Following Surgery

Primary Purpose

Osteoarthritis, Knee

Status
Completed
Phase
Phase 4
Locations
India
Study Type
Interventional
Intervention
Tapentadol 100 MG Oral Tablet
Pregabalin 150mg
Sponsored by
All India Institute of Medical Sciences, Bhubaneswar
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Osteoarthritis, Knee focused on measuring OA knee,pre-emptive analgesia,TKA,Opioids,gabapentinoids

Eligibility Criteria

18 Years - 65 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • 1. Patients both males and females undergoing total knee arthroplasty surgery. 2. Patients are capable of providing an informed consent. 3. Age group between 18-75 years.

Exclusion Criteria:

  • 1.Patients with asthma, COPD or any other respiratory disease. 2. Persistent nausea and vomiting at time of randomization 3. Epilepsy. 4. Treated with mono amine oxidase inhibitors, tricyclic antidepressants, serotonin norepinephrine re-uptake inhibitors, gabapentinoids.

    5. Patient with known neurological/ neuropsychiatric disorders. 6. Drug or alcohol abuse history 7. Opioid tolerance or opioid dependence. 8. Known history of opioid allergy or pregabalin allergy. 9. Renal disease (creatinine >1.5mg/dl) 10. Liver disease (total bilirubin >1.5mg/dl) 11. Pregnancy and lactation. 12. Cardiovascular insufficiency. 13. Patient with potential serotonin syndrome. 14. Patient with history of constipation and prone to paralytic ileus.

Sites / Locations

  • All India Institute of Medical Sciences

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Experimental

Arm Label

Pregabalin

Tapentadol

Arm Description

Pregabalin 150mg oral tablets before one hour before undergoing unilateral total knee arthroplasty

tapentadol 100mg oral tablets before one hour before undergoing unilateral total knee arthroplasty

Outcomes

Primary Outcome Measures

Efficacy and safety of pregabalin and tapentadol by measuring the mean difference in the mean VAS score.
Visual analogue scale (VAS) from 0 to 100 mm score at 0,6,12,24 hrs. post operatively in both the groups.

Secondary Outcome Measures

Comparing differences in TOTPAR scale through different time points of 24 hours Comparing differences in TOTPAR (none, mild, moderate and severe) scale through different time points of 24 hours
Scoring on TOTPAR scale at 0,6,12,24 hrs. post operatively in both the groups
Measuring the rescue analgesic requirement in both the groups
Mean difference in total analgesic consumption in both the groups post operatively
Monitoring adverse events in both the groups including post-operative nausea vomiting (PONV)
Frequency of nausea and vomiting in both the groups.
Percentage of adverse events in a 4-point verbal scale.
On a scale (None, Mild, Moderate, Severe) in both the groups.
Estimation of COX-2 at 0hrs and 6hrs post operatively in both the groups by ELISA.
Estimated in both the groups by ELISA.
Reduction of VAS and nausea/vomiting
Reduction of VAS to 3 at the end of 6 hours and 12 hours without nausea and vomiting

Full Information

First Posted
July 19, 2018
Last Updated
June 24, 2020
Sponsor
All India Institute of Medical Sciences, Bhubaneswar
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1. Study Identification

Unique Protocol Identification Number
NCT03604354
Brief Title
Safety and Efficacy of Pre-emptive Tapentadol vs Pregabalin in Post Operative Pain Following Surgery
Official Title
Safety and Efficacy of Pre-emptive Tapentadol vs Pregabalin in Post Operative Pain Following Unilateral Total Knee Arthroplasty- A Randomised, Double Blind, Active Control, Clinical Trial
Study Type
Interventional

2. Study Status

Record Verification Date
June 2020
Overall Recruitment Status
Completed
Study Start Date
August 1, 2018 (Actual)
Primary Completion Date
March 24, 2020 (Actual)
Study Completion Date
May 19, 2020 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
All India Institute of Medical Sciences, Bhubaneswar

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
Preemptive analgesia is a treatment modality which starts even before the surgery, so that the central sensitization is prevented due to incisional injury at the time of surgery, so it covers the period of surgery and initial post-operative period preventing the development of central sensitization. Gabapentinoid compounds are gabapentin and pregabalin which have been extensively used in seizure disorder patient. Role of gabapentinoid compounds in the management of pain, as a pre-emptive analgesia is yet to be completely evaluated in post operative pain. Opioids have always been the preferred drugs to manage post operative pain. Since opioids have major side effects of nausea vomiting associated with its treatment their use comes with management of these side effects. Currently, diagnostic and therapeutic approaches to manage pain experienced by individuals are limited especially because there's a lack of bio-markers predictive of therapeutic outcome. In search of an objective method for pain measurement, as pain has always been subjective and it is perceived by different people differently the study will also include finding the use of COX(cyclo-oxygenase)-2 as a bio-marker of pain in post-operative patients. Although several randomized clinical trials and met-analyses have been conducted comparing the safety and efficacy of tapentadol or pregabalin in post-operative pain, there is no head to head clinical trial conducted comparing the preemptive use of two drugs for postoperative pain following total knee arthroplasty (TKA). Hence the present study is planned.
Detailed Description
MATERIALS AND METHODS After approval of the institutional Ethics committee board, written informed consent will be taken from all the eligible and willing patients. A. Study design: Randomized double blind active controlled parallel group noninferiority clinical trial. B. Randomization: A variable block randomization. The allocation ratio will be 1:1 ratio between two interventions arms i.e. tapentadol 100 mg(milligram) and pregabalin 150 mg(milligram) orally. C. Allocation concealment: This study will be participant and investigator blinded. Allocation concealment will be done by sequentially numbered sealed drug pouches. D. Study site: Department of Pharmacology and Orthopedics of AIIMS, Bhubaneswar. Selection Criteria A. Inclusion criteria Patients both males and females undergoing total knee arthroplasty surgery. Patients are capable of providing an informed consent. Age group between 18-75 years. B. Exclusion criteria Patients with asthma, COPD(Chronic obstructive pulmonary disease) or any other respiratory disease. Persistent nausea and vomiting at time of randomization Epilepsy. Treated with mono amine oxidase inhibitors, tricyclic antidepressants, serotonin norepinephrine re-uptake inhibitors, gabapentinoids. Patient with known neurological/ neuropsychiatric disorders. Drug or alcohol abuse history Opioid tolerance or opioid dependence. Known history of opioid allergy or pregabalin allergy. Renal disease (creatinine >1.5mg/dl) Liver disease (total bilirubin >1.5mg/dl) Pregnancy and lactation. Cardiovascular insufficiency. Patient with potential serotonin syndrome. Patient with history of constipation and prone to paralytic ileus. Study procedure, tools & evaluation Consent: Patients will be explained the benefit and harm of joining the study and freedom of withdrawing from the study any moment they would like to. A full voluntary written informed consent will be obtained from each patient. Study will be conducted following the principles of Helsinki after getting written permission of the institutional ethics committee. Before enrolment of first patient in this study registration for clinical trial will be done. All the patients will be screened before enrollment after eliciting detailed history they will undergo complete medical and laboratory examinations. A total of 90 patients of either sex will be selected randomly and will be assigned to receive 100 mg of Tapentadol or 150mg Pregabalin orally 1hr before surgery in a double-blind manner. The patient will be assessed for pain at 0,6,12, and 24hrs, post operatively by visual analogue scale score(VAS) (0-100). Pain measurements will also be done on TOTPAR scale at 0,6,12,24 hours. Total rescue analgesic consumption also will be assessed at 24hrs post operatively. All treatment emergent adverse events will be documented. The time to 1st patient request for supplemental analgesia also will be recorded. A blood sample will be obtained from each of the patients twice once at 0 hrs. and again at 6hrs post operatively to evaluate concentration of COX-2 levels by ELISA with commercially available ELISA kits.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Osteoarthritis, Knee
Keywords
OA knee,pre-emptive analgesia,TKA,Opioids,gabapentinoids

7. Study Design

Primary Purpose
Prevention
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Masking Description
This study will be participant and investigator blinded. Allocation concealment will be done by sequentially numbered sealed drug pouches.
Allocation
Randomized
Enrollment
95 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Pregabalin
Arm Type
Active Comparator
Arm Description
Pregabalin 150mg oral tablets before one hour before undergoing unilateral total knee arthroplasty
Arm Title
Tapentadol
Arm Type
Experimental
Arm Description
tapentadol 100mg oral tablets before one hour before undergoing unilateral total knee arthroplasty
Intervention Type
Drug
Intervention Name(s)
Tapentadol 100 MG Oral Tablet
Intervention Description
This arm will receive drugs one hour before undergoing unilateral total knee arthroplasty. Interventions tapentadol 100mg oral tablets.
Intervention Type
Drug
Intervention Name(s)
Pregabalin 150mg
Intervention Description
This arm will receive drugs one hour before undergoing unilateral total knee arthroplasty. Interventions pregabalin 150mg oral tablets.
Primary Outcome Measure Information:
Title
Efficacy and safety of pregabalin and tapentadol by measuring the mean difference in the mean VAS score.
Description
Visual analogue scale (VAS) from 0 to 100 mm score at 0,6,12,24 hrs. post operatively in both the groups.
Time Frame
Evaluated over 24hrs post unilateral total knee arthroplasty
Secondary Outcome Measure Information:
Title
Comparing differences in TOTPAR scale through different time points of 24 hours Comparing differences in TOTPAR (none, mild, moderate and severe) scale through different time points of 24 hours
Description
Scoring on TOTPAR scale at 0,6,12,24 hrs. post operatively in both the groups
Time Frame
Recorded over 24hrs post unilateral total knee arthroplasty
Title
Measuring the rescue analgesic requirement in both the groups
Description
Mean difference in total analgesic consumption in both the groups post operatively
Time Frame
Recorded over 24hrs post unilateral total knee arthroplasty
Title
Monitoring adverse events in both the groups including post-operative nausea vomiting (PONV)
Description
Frequency of nausea and vomiting in both the groups.
Time Frame
Recorded over 24hrs post unilateral total knee arthroplasty
Title
Percentage of adverse events in a 4-point verbal scale.
Description
On a scale (None, Mild, Moderate, Severe) in both the groups.
Time Frame
Recorded over 24hrs post unilateral total knee arthroplasty
Title
Estimation of COX-2 at 0hrs and 6hrs post operatively in both the groups by ELISA.
Description
Estimated in both the groups by ELISA.
Time Frame
In two blood samples one at 0hrs and 6hrs post operatively
Title
Reduction of VAS and nausea/vomiting
Description
Reduction of VAS to 3 at the end of 6 hours and 12 hours without nausea and vomiting
Time Frame
Evaluated at the end of 6 hours and 12 hours without nausea and vomiting

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: 1. Patients both males and females undergoing total knee arthroplasty surgery. 2. Patients are capable of providing an informed consent. 3. Age group between 18-75 years. Exclusion Criteria: 1.Patients with asthma, COPD or any other respiratory disease. 2. Persistent nausea and vomiting at time of randomization 3. Epilepsy. 4. Treated with mono amine oxidase inhibitors, tricyclic antidepressants, serotonin norepinephrine re-uptake inhibitors, gabapentinoids. 5. Patient with known neurological/ neuropsychiatric disorders. 6. Drug or alcohol abuse history 7. Opioid tolerance or opioid dependence. 8. Known history of opioid allergy or pregabalin allergy. 9. Renal disease (creatinine >1.5mg/dl) 10. Liver disease (total bilirubin >1.5mg/dl) 11. Pregnancy and lactation. 12. Cardiovascular insufficiency. 13. Patient with potential serotonin syndrome. 14. Patient with history of constipation and prone to paralytic ileus.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Debasish Hota, MD;DM
Organizational Affiliation
AIIMS BHUBANESWAR
Official's Role
Principal Investigator
Facility Information:
Facility Name
All India Institute of Medical Sciences
City
Bhubaneswar
State/Province
Odisha
ZIP/Postal Code
751019
Country
India

12. IPD Sharing Statement

Plan to Share IPD
No
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Safety and Efficacy of Pre-emptive Tapentadol vs Pregabalin in Post Operative Pain Following Surgery

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