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

Sponsor
Asian Institute of Gastroenterology, India (Other)
Overall Status
Completed
CT.gov ID
NCT01528540
Collaborator
(none)
87
1
2
32
2.7

Study Details

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.

Condition or Disease Intervention/Treatment Phase
  • Drug: Placebo
  • Drug: Antioxidant plus Pregabalin
N/A

Study Design

Study Type:
Interventional
Actual Enrollment :
87 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Triple (Participant, Care Provider, Investigator)
Primary Purpose:
Treatment
Official Title:
Evaluation of Efficacy of Combination of Pregabalin and Antioxidant in Reducing Pain in Chronic Pancreatitis: a RCT
Study Start Date :
Apr 1, 2012
Actual Primary Completion Date :
Dec 1, 2014
Actual Study Completion Date :
Dec 1, 2014

Arms and Interventions

Arm Intervention/Treatment
Placebo Comparator: Placebo

This group will contain a placebo for antioxidant cocktail and pregabalin

Drug: Placebo
This group will include placebo.

Experimental: Antioxidant plus pregabalin

This group will contain antioxidant cocktail and pregabalin

Drug: Antioxidant plus Pregabalin
This group will contain combination of antioxidant cocktail and pregabalin

Outcome Measures

Primary Outcome Measures

  1. Change in the pain score [Baseline and 8weeks]

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

Secondary Outcome Measures

  1. Change in number of painful days [Baseline and 8weeks]

    The number of days of pain per week will be measured.

  2. Change in analgesic requirement [Baseline and 8weeks]

    The type (opiate/non-opiate), number and route of additional analgesic medicines that were required within the study period will be evaluated.

  3. Change in quality of life [Baseline and 8weeks]

    QOL will be evaluated with the EORTC QLQ-C30/PAN26 questionnaire

  4. Change in depression scale [Baseline and 8weeks]

    Depression will be assessed with the Beck's Depression Inventory.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 65 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
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

Contacts and Locations

Locations

Site City State Country Postal Code
1 Asian Institute of Gastroenterology Hyderabad Andhra Pradesh India 500082

Sponsors and Collaborators

  • Asian Institute of Gastroenterology, India

Investigators

  • Principal Investigator: Rupjyoti Talukdar, MD, Asian Institue of Gastroenterology

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Asian Institute of Gastroenterology, India
ClinicalTrials.gov Identifier:
NCT01528540
Other Study ID Numbers:
  • AIG-PAN-2012-1
First Posted:
Feb 8, 2012
Last Update Posted:
Sep 9, 2015
Last Verified:
Sep 1, 2015
Keywords provided by Asian Institute of Gastroenterology, India
Additional relevant MeSH terms:

Study Results

No Results Posted as of Sep 9, 2015