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Evaluation of Efficacy of Combination of Pregabalin and Antioxidant in Reducing Pain in Chronic Pancreatitis: a Randomized Control Trial

Primary Purpose

Chronic Pancreatitis

Status
Completed
Phase
Not Applicable
Locations
India
Study Type
Interventional
Intervention
Placebo
Antioxidant plus Pregabalin
Sponsored by
Asian Institute of Gastroenterology, India
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Chronic Pancreatitis focused on measuring chronic pancreatitis, pregabalin, antioxidant

Eligibility Criteria

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

Inclusion Criteria:

  1. Epigastric pain +/- radiation at least thrice in one month over the past three month.
  2. Endotherapy/Surgery and ducal clearance

Exclusion Criteria:

  1. Age <18 and >65yrs
  2. MPD and biliary obstruction
  3. Pancreatic neoplastic lesions
  4. Acute flare
  5. Pancreatic pseudocysts
  6. Pregnancy
  7. Cardiac and renal diseases
  8. Use of other anti epileptics
  9. Hypersensitivity to gabapentin/pregabalin

Sites / Locations

  • Asian Institute of Gastroenterology

Arms of the Study

Arm 1

Arm 2

Arm Type

Placebo Comparator

Experimental

Arm Label

Placebo

Antioxidant plus pregabalin

Arm Description

This group will contain a placebo for antioxidant cocktail and pregabalin

This group will contain antioxidant cocktail and pregabalin

Outcomes

Primary Outcome Measures

Change in the pain score
Pain score will be assessed by the Izbicki pain score, Visual analog scale and painDETECT tool for neuropathic pain.

Secondary Outcome Measures

Change in number of painful days
The number of days of pain per week will be measured.
Change in analgesic requirement
The type (opiate/non-opiate), number and route of additional analgesic medicines that were required within the study period will be evaluated.
Change in quality of life
QOL will be evaluated with the EORTC QLQ-C30/PAN26 questionnaire
Change in depression scale
Depression will be assessed with the Beck's Depression Inventory.

Full Information

First Posted
January 27, 2012
Last Updated
September 8, 2015
Sponsor
Asian Institute of Gastroenterology, India
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1. Study Identification

Unique Protocol Identification Number
NCT01528540
Brief Title
Evaluation of Efficacy of Combination of Pregabalin and Antioxidant in Reducing Pain in Chronic Pancreatitis: a Randomized Control Trial
Official Title
Evaluation of Efficacy of Combination of Pregabalin and Antioxidant in Reducing Pain in Chronic Pancreatitis: a RCT
Study Type
Interventional

2. Study Status

Record Verification Date
September 2015
Overall Recruitment Status
Completed
Study Start Date
April 2012 (undefined)
Primary Completion Date
December 2014 (Actual)
Study Completion Date
December 2014 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Asian Institute of Gastroenterology, India

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Study hypothesis: Combination of antioxidants and pregabalin results in better pain relief than placebo in patients with chronic pancreatitis. Chronic pancreatitis (CP) is a clinical enigma, with pain being the most distressing symptom that brings the patient to clinical attention. Pain in chronic pancreatitis is multifactorial, and may be related to pancreatic ductal hypertension, tissue hypertension, inflammatory cytokines, oxidative stress and neuropathic mechanisms like mechanical allodynia, inflammatory hyperalgesia and temporal summation. The mainstay of treatment for pain in CP due to pancreatic ductal stone is endotherapy (ESWL and ERCP). Recent randomized controlled trials have shown that antioxidant cocktail and pregabalin (a presynaptic voltage gated calcium channel blocking agent) can result in significant reduction of pain in CP. In this study, the investigators will study the efficacy of the combination of antioxidants and pregabalin in reducing pain and compare that with placebo. The investigators will randomize patients with documented chronic pancreatitis with recurrent/persistent pain after undergoing endotherapy and ductal clearance into three groups: Group A- antioxidants + pregabalin; Group B- Placebo. The primary outcome will be change in pain score and the secondary outcomes will be change in the number of painful days, analgesic requirements, quality of life and depression scale. Pain score will be quantified by the Izbicki pain score and visual analog scale; while quality of life and depression will be measured by the EORTC QLQ-C30/PAN26 and Beck depression inventory respectively. Comparison between Group A vs B will be made by the Chi square test/Fischer Exact and the Student's 't' tests respectively and analysis will be done on a intention to treat and per protocol basis. With an expected improvement of pain by 40% (at 80% power and alpha of 0.05) and adjusting for a presumed 10% drop out rate, the required sample size in each group will be at least 40.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Chronic Pancreatitis
Keywords
chronic pancreatitis, pregabalin, antioxidant

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigator
Allocation
Randomized
Enrollment
87 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
This group will contain a placebo for antioxidant cocktail and pregabalin
Arm Title
Antioxidant plus pregabalin
Arm Type
Experimental
Arm Description
This group will contain antioxidant cocktail and pregabalin
Intervention Type
Drug
Intervention Name(s)
Placebo
Intervention Description
This group will include placebo.
Intervention Type
Drug
Intervention Name(s)
Antioxidant plus Pregabalin
Intervention Description
This group will contain combination of antioxidant cocktail and pregabalin
Primary Outcome Measure Information:
Title
Change in the pain score
Description
Pain score will be assessed by the Izbicki pain score, Visual analog scale and painDETECT tool for neuropathic pain.
Time Frame
Baseline and 8weeks
Secondary Outcome Measure Information:
Title
Change in number of painful days
Description
The number of days of pain per week will be measured.
Time Frame
Baseline and 8weeks
Title
Change in analgesic requirement
Description
The type (opiate/non-opiate), number and route of additional analgesic medicines that were required within the study period will be evaluated.
Time Frame
Baseline and 8weeks
Title
Change in quality of life
Description
QOL will be evaluated with the EORTC QLQ-C30/PAN26 questionnaire
Time Frame
Baseline and 8weeks
Title
Change in depression scale
Description
Depression will be assessed with the Beck's Depression Inventory.
Time Frame
Baseline and 8weeks

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: Epigastric pain +/- radiation at least thrice in one month over the past three month. Endotherapy/Surgery and ducal clearance Exclusion Criteria: Age <18 and >65yrs MPD and biliary obstruction Pancreatic neoplastic lesions Acute flare Pancreatic pseudocysts Pregnancy Cardiac and renal diseases Use of other anti epileptics Hypersensitivity to gabapentin/pregabalin
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Rupjyoti Talukdar, MD
Organizational Affiliation
Asian Institue of Gastroenterology
Official's Role
Principal Investigator
Facility Information:
Facility Name
Asian Institute of Gastroenterology
City
Hyderabad
State/Province
Andhra Pradesh
ZIP/Postal Code
500082
Country
India

12. IPD Sharing Statement

Citations:
PubMed Identifier
18952082
Citation
Bhardwaj P, Garg PK, Maulik SK, Saraya A, Tandon RK, Acharya SK. A randomized controlled trial of antioxidant supplementation for pain relief in patients with chronic pancreatitis. Gastroenterology. 2009 Jan;136(1):149-159.e2. doi: 10.1053/j.gastro.2008.09.028. Epub 2008 Sep 25.
Results Reference
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PubMed Identifier
21683078
Citation
Olesen SS, Bouwense SA, Wilder-Smith OH, van Goor H, Drewes AM. Pregabalin reduces pain in patients with chronic pancreatitis in a randomized, controlled trial. Gastroenterology. 2011 Aug;141(2):536-43. doi: 10.1053/j.gastro.2011.04.003. Epub 2011 Apr 14.
Results Reference
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Evaluation of Efficacy of Combination of Pregabalin and Antioxidant in Reducing Pain in Chronic Pancreatitis: a Randomized Control Trial

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