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Intraoperative Coeliac Plexus Alcohol Neurolysis Along With Frey's Procedure for a Better Pain Relief (INFARCT)

Primary Purpose

Chronic Calcific Pancreatitis

Status
Unknown status
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
celiac plexus neurolysis using absolute alcohol
Placebo celiac plexus injection using saline
Frey's procedure
Sponsored by
Madras Medical College
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Chronic Calcific Pancreatitis focused on measuring CCP

Eligibility Criteria

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

Inclusion Criteria:

  • Consecutive chronic calcific pancreatitis admitted in our institute since 2013 january with age group between 13 to 65 years with Visual analogue scale (VAS) pain score of more than 7 and those who have quit alcohol & smoking for at least 6 months are included in our study.

Exclusion Criteria:

  • Patients with mild to moderate pain score (VAS pain score 1-7), continuous substance abuse, severe comorbid illness are excluded from study.

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm Type

    Active Comparator

    Placebo Comparator

    Arm Label

    GROUP 1

    GROUP 2

    Arm Description

    68 Patients undergo Frey's procedure with celiac plexus neurolysis using absolute alcohol

    68 Patients undergo Frey's procedure with Placebo celiac plexus injection using saline

    Outcomes

    Primary Outcome Measures

    Pain relief measured by Visual Analogue Scale
    Short term (2 years) and long term(5 years) score at follow up at out patient clinic or over phone.

    Secondary Outcome Measures

    Number of patients with improvement in endocrine function as measured by Fasting glucose of < 130 and HbA1c level of <6.5%
    and reduction in dosage of insulin (iu) & oral hypoglycemic agents (milli gm) when compared to preoperative levels- at out patient clinic
    Number of patients with improvement or worsening in exocrine function as measured by the estimation of fecal elastase >200 µg/g of stool or <200 µg/g of stool respectively at out patient clinic.
    Analgesics intake
    Dosage and frequency of intake of both NSAIDs and opioid analgesics intake are noted at out patient clinic or over phone.
    Weight gain in kg measured at out patient clinic
    Quality of life
    Using SF 12 V2 (Tamil and english version-Optuminsight Life Sciences) in a face to face (written form) interview at out patient clinic
    Number of patients with worsening in endocrine function as measured by abnormal laboratory values like Fasting glucose >130 and HbA1c >6.5
    and increased dosage of insulin (IU)& oral hypoglycemic agents(milli gms) requirement when compared to preoperative levels at out patient clinic
    Number of patients with abnormal lab values like Fasting glucose of >126 mg/dl or blood glucose level of >200 after a standard glucose tolerance test (GTT) in equivocal cases.

    Full Information

    First Posted
    March 16, 2016
    Last Updated
    April 11, 2016
    Sponsor
    Madras Medical College
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    1. Study Identification

    Unique Protocol Identification Number
    NCT02735330
    Brief Title
    Intraoperative Coeliac Plexus Alcohol Neurolysis Along With Frey's Procedure for a Better Pain Relief
    Acronym
    INFARCT
    Official Title
    Intra Operative Coeliac Plexus Neurolysis Combined With Frey's Procedure for Effective Pain Relief in Patients With Chronic Calcific Pancreatitis- A Prospective Randomized Double-blind Placebo Controlled Trial
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    April 2016
    Overall Recruitment Status
    Unknown status
    Study Start Date
    January 2013 (undefined)
    Primary Completion Date
    December 2015 (Actual)
    Study Completion Date
    September 2019 (Anticipated)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Principal Investigator
    Name of the Sponsor
    Madras Medical College

    4. Oversight

    Data Monitoring Committee
    Yes

    5. Study Description

    Brief Summary
    To study the effect of Intra operative Coeliac plexus alcohol neurolysis combined with Frey's procedure for effective pain relief in patients with Chronic Calcific Pancreatitis in a single centre setting with a Randomized Controlled Trial.
    Detailed Description
    165 consecutive CCP patients admitted in our surgical gastro enterology department since January 2013 were screened for eligibility. 29 patients were excluded (28 were not meeting the inclusion criteria and 1 patient intra operatively found to have disseminated malignancy). After exclusion 136 patients were included in our study. They were randomized in to 2 groups, one group was treated by Frey's procedure with NCPB (Group-I) and the other by Frey's procedure with saline as placebo (Group-II). Method of Study is a randomized, double- blind, placebo- controlled, parallel arm, superiority trial. Randomization was done at the time of surgery using random number table created with computerized software by a statistician not involved in this study. Blinding and masking was done by using pre numbered containers having filled with either absolute alcohol or saline according to the randomization chart which was then kept sealed by an office staff until the end of the study. Both subjects and response assessor were blinded. Data collection: The preoperative baseline details such as etiology, morphology, associated complications and VAS pain score, Izbicki pain score, weight loss, insulin requirement, LFT (liver function tests), serum amylase & lipase, fasting sugar& fecal elastase were collected on admission. Additional procedures, presence of peripancreatic inflammatory changes (fibrosis) as evidenced by difficult Kocherisation and plasted capsule and intra-operative complications were noted during surgery. Short term follow up details including pain relief measured by VAS score &Izbicki pain score, analgesic consumption, weight gain, improvement in steatorrhoea (Fecal elastase>200 µg/g of stool & subjective reduction in foul smelling oily diarrhea), diabetic status (fasting glucose, GTT, HgbA1c, insulin& oral hypoglycemic agents requirement), mortality and morbidity were noted. Follow up details were collected every 3 months as outpatient basis. Standard questionnaire format of SF 12 Version-2 was used for QOL assessment every 6 months in a face to face interview. Statistical analysis was performed in SPSS version 20. Continuous variables were presented as mean, standard deviation and 95% confidence interval; categorical variables were presented as frequencies. The chi-square test and the Fisher exact test were used to analyze categorical variables. The unpaired Student t test was used to analyze continuous variables. P value <0.05 was considered statistically significant. Factors found significant on univariate logistic regression analysis were incorporated in to the multivariate logistic regression analysis for odds ratio with 95% confidence intervals to analyze the significant factors affecting the outcome of surgery.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Chronic Calcific Pancreatitis
    Keywords
    CCP

    7. Study Design

    Primary Purpose
    Treatment
    Study Phase
    Not Applicable
    Interventional Study Model
    Parallel Assignment
    Masking
    ParticipantCare ProviderInvestigatorOutcomes Assessor
    Allocation
    Randomized
    Enrollment
    136 (Actual)

    8. Arms, Groups, and Interventions

    Arm Title
    GROUP 1
    Arm Type
    Active Comparator
    Arm Description
    68 Patients undergo Frey's procedure with celiac plexus neurolysis using absolute alcohol
    Arm Title
    GROUP 2
    Arm Type
    Placebo Comparator
    Arm Description
    68 Patients undergo Frey's procedure with Placebo celiac plexus injection using saline
    Intervention Type
    Procedure
    Intervention Name(s)
    celiac plexus neurolysis using absolute alcohol
    Other Intervention Name(s)
    NCPB, Neurolytic celiac plexus block
    Intervention Description
    celiac plexus blockade with 40 ml of diluted absolute alcohol(50%) 20 ml on either side of celiac axis in a 4 quadrant fashion
    Intervention Type
    Procedure
    Intervention Name(s)
    Placebo celiac plexus injection using saline
    Other Intervention Name(s)
    Placebo
    Intervention Description
    Placebo celiac plexus injection with 40 ml of saline 20 ml on either side of celiac axis in a 4 quadrant fashion for blinding
    Intervention Type
    Procedure
    Intervention Name(s)
    Frey's procedure
    Other Intervention Name(s)
    Duodenum preserving pancreatic head coring procedure
    Intervention Description
    Pancreatic head is partially resected (cored) along with longitudinal opening of duct along its entire length with limit of excavation of the head in the plane of the posterior wall of the Wirsung's duct and duct of Santorini is opened in the uncinate process. All the tissue above the plane, including the duct of Santorini is excised. The reconstruction is done with covering with a loop of jejunum in Roux-en-Y fashion which continues with the main pancreatic duct in the pancreatic body and tail.
    Primary Outcome Measure Information:
    Title
    Pain relief measured by Visual Analogue Scale
    Description
    Short term (2 years) and long term(5 years) score at follow up at out patient clinic or over phone.
    Time Frame
    up to 5 years
    Secondary Outcome Measure Information:
    Title
    Number of patients with improvement in endocrine function as measured by Fasting glucose of < 130 and HbA1c level of <6.5%
    Description
    and reduction in dosage of insulin (iu) & oral hypoglycemic agents (milli gm) when compared to preoperative levels- at out patient clinic
    Time Frame
    up to 5 years
    Title
    Number of patients with improvement or worsening in exocrine function as measured by the estimation of fecal elastase >200 µg/g of stool or <200 µg/g of stool respectively at out patient clinic.
    Time Frame
    up to 5 years
    Title
    Analgesics intake
    Description
    Dosage and frequency of intake of both NSAIDs and opioid analgesics intake are noted at out patient clinic or over phone.
    Time Frame
    up to 5 years
    Title
    Weight gain in kg measured at out patient clinic
    Time Frame
    up to 5 years
    Title
    Quality of life
    Description
    Using SF 12 V2 (Tamil and english version-Optuminsight Life Sciences) in a face to face (written form) interview at out patient clinic
    Time Frame
    up to 5 years
    Title
    Number of patients with worsening in endocrine function as measured by abnormal laboratory values like Fasting glucose >130 and HbA1c >6.5
    Description
    and increased dosage of insulin (IU)& oral hypoglycemic agents(milli gms) requirement when compared to preoperative levels at out patient clinic
    Time Frame
    up to 5 years
    Title
    Number of patients with abnormal lab values like Fasting glucose of >126 mg/dl or blood glucose level of >200 after a standard glucose tolerance test (GTT) in equivocal cases.
    Time Frame
    up to 5 years
    Other Pre-specified Outcome Measures:
    Title
    Frequency of pain attacks
    Description
    whether pain attacks are occurring in a daily/several times in a week/month/Year is noted.
    Time Frame
    Up to 5 years
    Title
    Time of disease related inability to work
    Description
    Whether the restriction of work activities last permanently/ Up to 1 year/month/week or no restriction is noted
    Time Frame
    Up to 5 years
    Title
    Type of analgesic medication (morphine related analgesic potency)
    Description
    What analgesic medication is taken by the patient like morphine,pethidine,buprenorphine, tramadol,aspirin, paracetamol are noted.
    Time Frame
    Up to 5 years

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    13 Years
    Maximum Age & Unit of Time
    65 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: Consecutive chronic calcific pancreatitis admitted in our institute since 2013 january with age group between 13 to 65 years with Visual analogue scale (VAS) pain score of more than 7 and those who have quit alcohol & smoking for at least 6 months are included in our study. Exclusion Criteria: Patients with mild to moderate pain score (VAS pain score 1-7), continuous substance abuse, severe comorbid illness are excluded from study.
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    KANNAN DEVYGOUNDER, MS,MCh,FRCS
    Organizational Affiliation
    MADRAS MEDICAL COLLEGE,CHENNAI,TAMIL NADU,INDIA
    Official's Role
    Study Director
    First Name & Middle Initial & Last Name & Degree
    BALAKUMARAN SATHYAMOORTHY
    Organizational Affiliation
    MADRAS MEDICAL COLLEGE,CHENNAI,TAMIL NADU, INDIA
    Official's Role
    Principal Investigator

    12. IPD Sharing Statement

    Plan to Share IPD
    Yes
    IPD Sharing Plan Description
    with out showing the name of the participants we can disclose the data of the all participants

    Learn more about this trial

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