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
About this trial
This is an interventional treatment trial for Chronic Calcific Pancreatitis focused on measuring CCP
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.
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
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
Intraoperative Coeliac Plexus Alcohol Neurolysis Along With Frey's Procedure for a Better Pain Relief
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