search
Back to results

Pinaverium Bromide in Post-cholecystectomy Sphincter of Oddi Dysfunction

Primary Purpose

Sphincter of Oddi Dysfunction

Status
Unknown status
Phase
Phase 4
Locations
China
Study Type
Interventional
Intervention
Danshu Capsules
Pinaverium Bromide
Sponsored by
Xinhua Hospital, Shanghai Jiao Tong University School of Medicine
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Sphincter of Oddi Dysfunction focused on measuring Pinaverium Bromide, cholecystectomy, Sphincter of Oddi Dysfunction

Eligibility Criteria

18 Years - 69 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Chief complaint of upper right abdominal pain following LC (within 2 weeks to 6 months) at a hospital visit, but not a pain caused by surgical incision, lasting 3 to 5 minutes each time, without a history of other biliary tract operation
  • No presence of intestinal obstruction as evidenced by plain abdominal X-ray, with peptic ulcer and duodenal diverticulum ruled out through barium meal examination or gastroscopy
  • No other obvious abnormalities as evidenced by abdominal ultrasound B and MRCP, except for bile duct dilation
  • Patients with biliary-type sphincter of Oddi dysfunction (SOD) who are classified as SOD type II (biliary-type abdominal pain accompanied by hepatic enzyme elevation or common bile duct (CBD) dilation) and SOD type III (only biliary-type abdominal pain) according to Geenen-Hogan classification criteria

Exclusion Criteria:

  • Postoperative biliary calculi, benign biliary stenosis, bile duct infection, overlong residual cystic duct (> 0.5cm), biliary tumors, etc.
  • Peptic ulcer, duodenal diverticulum
  • Pancreatitis, pancreatic-type SOD
  • Adhesive intestinal obstruction
  • Postoperative irritable bowel syndrome (IBS)
  • A history of abdominal operation or other surgery
  • Pregnant and lactating women
  • Use of other drugs from one week after LC to enrollment, including antispasmodic drugs, analgesics, choleretic agents, calcium ion antagonists and GI motility drugs
  • A history of allergy to Pinaverium Bromide / Danshu Tablets

Sites / Locations

  • Zhang YongRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Pinaverium Bromide group

Danshu group

Arm Description

Able to improve the spasms of SO; literature showed that it treated biliary disorders effectively.

Contains the active pharmaceutical ingredient (API) and has the effects of fighting infection, alleviating pain, promoting bile secretion and lifting muscle spasms; literature showed that Danshu Capsules effectively improved the symptoms of biliary disorders, such as pain, nausea and abdominal distension.

Outcomes

Primary Outcome Measures

Efficacy Evaluation of Reduction in Abdominal Pain Scores,Change From Baseline to 3 Months After Medication
abdominal pain scores (baseline vs. 3 months after treatment) Abdominal pain score based on main symptom: Degree of pain in point(0 - no pain [0 point];1~3 - mild pain [1 point];4~6 moderate pain [2 point]];7~10 - severe pain [3 point])、Frequency in times/week (No episodes[0 point];1 time/week[1 point];2 times/week[2 point]; 3 times/week[3 point])、Duration in days/week(No episodes[0 point];< 1 day/week[1 point];1-2days/week[2 points];≥ 3days/week[3 points]) The sum of the scores for the above three items is the total score for abdominal pain. Efficacy evaluation: reduction in abdominal pain score, as compared with the baseline = 100%: complete remission (CR);60%~99%: significant remission (SR);30% ~ 59%: partial remission (PR);0% ~ 29%: no response (NR) Treatment response = CR + SR Treatment response rate = (CR + SR) / the total number of patients

Secondary Outcome Measures

Changes in the Common Bile Duct (CBD) Diameter Measured by Ultrasound B Once a Month
Changes in the CBD diameter measured by ultrasound B Each patient is required to abstain from eating for 12 hours and then takes a measurement of the CBD diameter by ultrasound B the next morning The measurement takes places once a month, four times totally (baseline / 4w after treatment / 8w after treatment / 12w after treatment)
Efficacy of Lowering Liver Enzymes as Assessed by Laboratory Test Once a Month
Changes in hepatic enzyme levels (ALT, AST and ALP) The measurement takes place once a month, four times totally (baseline / 4w after treatment / 8w after treatment / 12w after treatment)
Number of Participants With Treatment-Related Diarrhea,Change From Baseline to 3 Months After Medication
The number of patients presenting the symptoms of diarrhea will be calculated at the time of enrollment (baseline) and 3 months after treatment respectively.

Full Information

First Posted
July 4, 2016
Last Updated
July 11, 2016
Sponsor
Xinhua Hospital, Shanghai Jiao Tong University School of Medicine
search

1. Study Identification

Unique Protocol Identification Number
NCT02833103
Brief Title
Pinaverium Bromide in Post-cholecystectomy Sphincter of Oddi Dysfunction
Official Title
Application of Pinaverium Bromide in the Treatment of Patients With Post-cholecystectomy Sphincter of Oddi Dysfunction (SOD): A Randomized, Controlled and Multicenter Clinical Study
Study Type
Interventional

2. Study Status

Record Verification Date
July 2016
Overall Recruitment Status
Unknown status
Study Start Date
July 2016 (undefined)
Primary Completion Date
February 2018 (Anticipated)
Study Completion Date
February 2018 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Xinhua Hospital, Shanghai Jiao Tong University School of Medicine

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Sphincter of Oddi dysfunction (SOD) refers to biliary kinetic abnormality of the sphincter of Oddi (SO), often accompanied by pain, hepatic and pancreatic enzyme elevation, common bile duct (CBD) dilation or onset of pancreatitis. Pain caused by SOD affects the quality of life (QoL).The primary objective of this trial is to evaluate the efficacy of relieving abdominal pain of Pinaverium Bromide in medication therapy for patients with post-cholecystectomy SOD.
Detailed Description
1.1 Background (I) 1.1.1 10%~50% of the patients who previously underwent cholecystectomy experience recurrent abdominal pain with or without diarrhea, abdominal distention, enzymatic changes, etc., and sphincter of Oddi dysfunction (SOD) accounts for about 13% of such cases; 1.1.2 Sphincter of Oddi dysfunction (SOD): It refers to biliary kinetic abnormality of the sphincter of Oddi (SO), often accompanied by pain, hepatic and pancreatic enzyme elevation, common bile duct (CBD) dilation or onset of pancreatitis. Pain caused by SOD affects the quality of life (QoL). 1.1.3 The diagnosis of SOD is still being disputed, and there has been no optimal solution so far. The diagnosis of SOD is largely based on clinical judgment The gold standards ERCP and SOM are invasive diagnostic criteria 1.2 Background (II) 1.2.1 If biliary-type abdominal pain after cholecystectomy is considered as SOD, most of the patients are classified as SOD II and SOD III according to Rome III Criteria-modified. Biliary SOD Type I: moderate or severe biliary-type abdominal pain; transient ALT / AST/ALP elevation > 2ULN; CBD dilation > 8mm as evidenced by ultrasound or other non-invasive examination Type II: biliary-type abdominal pain; One or two of above items Type III:only biliary-type abdominal pain 1.3 Background (III) 1.3.1 Treatment of SOD is being disputed: currently, the main method is to relax sphincter of Oddi (SO). Medications: antispasmodic drugs, nitrates, calcium ion antagonists, modulators of gastrointestinal (GI) motility EST(endoscopic sphincterotomy): postoperative complications and mortality 1.3.2 EST is not well effective in the treatment of SOD type II and type III, which are mostly caused by functional abnormalities -ASGE guideline 2015 points out that EST is not recommended for patients with SOD type III. Endoscopic stents are not recommended, either. 1.3.3 Danshu Capsules: contains the active pharmaceutical ingredient (API) and has the effects of fighting infection, alleviating pain, promoting bile secretion and lifting muscle spasms; literature showed that Danshu Capsules effectively improved the symptoms of biliary disorders, such as pain, nausea and abdominal distension. 1.3.4 Pinaverium Bromide: able to improve the spasms of SO; literature showed that it treated biliary disorders effectively.·10%~50% of the patients who previously underwent cholecystectomy experience recurrent abdominal pain with or without diarrhea, abdominal distention, enzymatic changes, etc., and sphincter of Oddi dysfunction (SOD) accounts for about 13% of such cases.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Sphincter of Oddi Dysfunction
Keywords
Pinaverium Bromide, cholecystectomy, Sphincter of Oddi Dysfunction

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
168 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Pinaverium Bromide group
Arm Type
Experimental
Arm Description
Able to improve the spasms of SO; literature showed that it treated biliary disorders effectively.
Arm Title
Danshu group
Arm Type
Active Comparator
Arm Description
Contains the active pharmaceutical ingredient (API) and has the effects of fighting infection, alleviating pain, promoting bile secretion and lifting muscle spasms; literature showed that Danshu Capsules effectively improved the symptoms of biliary disorders, such as pain, nausea and abdominal distension.
Intervention Type
Drug
Intervention Name(s)
Danshu Capsules
Other Intervention Name(s)
Danshu softgel Capsules
Intervention Description
Danshu Capsules (0.9g potid/day) for three months by oral
Intervention Type
Drug
Intervention Name(s)
Pinaverium Bromide
Other Intervention Name(s)
Dicetel
Intervention Description
Pinaverium Bromide (100mg potid/day) for three months by oral
Primary Outcome Measure Information:
Title
Efficacy Evaluation of Reduction in Abdominal Pain Scores,Change From Baseline to 3 Months After Medication
Description
abdominal pain scores (baseline vs. 3 months after treatment) Abdominal pain score based on main symptom: Degree of pain in point(0 - no pain [0 point];1~3 - mild pain [1 point];4~6 moderate pain [2 point]];7~10 - severe pain [3 point])、Frequency in times/week (No episodes[0 point];1 time/week[1 point];2 times/week[2 point]; 3 times/week[3 point])、Duration in days/week(No episodes[0 point];< 1 day/week[1 point];1-2days/week[2 points];≥ 3days/week[3 points]) The sum of the scores for the above three items is the total score for abdominal pain. Efficacy evaluation: reduction in abdominal pain score, as compared with the baseline = 100%: complete remission (CR);60%~99%: significant remission (SR);30% ~ 59%: partial remission (PR);0% ~ 29%: no response (NR) Treatment response = CR + SR Treatment response rate = (CR + SR) / the total number of patients
Time Frame
Change From Baseline to 3 Months After Medication
Secondary Outcome Measure Information:
Title
Changes in the Common Bile Duct (CBD) Diameter Measured by Ultrasound B Once a Month
Description
Changes in the CBD diameter measured by ultrasound B Each patient is required to abstain from eating for 12 hours and then takes a measurement of the CBD diameter by ultrasound B the next morning The measurement takes places once a month, four times totally (baseline / 4w after treatment / 8w after treatment / 12w after treatment)
Time Frame
Once a Month, Four Times Totally (baseline / 4w after treatment / 8w after treatment / 12w after treatment)
Title
Efficacy of Lowering Liver Enzymes as Assessed by Laboratory Test Once a Month
Description
Changes in hepatic enzyme levels (ALT, AST and ALP) The measurement takes place once a month, four times totally (baseline / 4w after treatment / 8w after treatment / 12w after treatment)
Time Frame
Once a Month, Four Times Totally (baseline / 4w after treatment / 8w after treatment / 12w after treatment)
Title
Number of Participants With Treatment-Related Diarrhea,Change From Baseline to 3 Months After Medication
Description
The number of patients presenting the symptoms of diarrhea will be calculated at the time of enrollment (baseline) and 3 months after treatment respectively.
Time Frame
From Baseline to 3 Months After Medication
Other Pre-specified Outcome Measures:
Title
Number of Participants With Treatment-Related Adverse Events as Assessed by Researchers or Doctors Through Study Completion
Description
Incidence of adverse events (throughout the treatment) The type and number of adverse events will be calculated at the baseline and each visit Inquire about symptoms: rashes, pruritus, acid regurgitation, abdominal distention, diarrhea, etc. Perform the following examinations at the last visit: blood / urine / stool test, liver / kidney function test, ECG
Time Frame
Through Study Completion, An Average of 1 Year

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
69 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Chief complaint of upper right abdominal pain following LC (within 2 weeks to 6 months) at a hospital visit, but not a pain caused by surgical incision, lasting 3 to 5 minutes each time, without a history of other biliary tract operation No presence of intestinal obstruction as evidenced by plain abdominal X-ray, with peptic ulcer and duodenal diverticulum ruled out through barium meal examination or gastroscopy No other obvious abnormalities as evidenced by abdominal ultrasound B and MRCP, except for bile duct dilation Patients with biliary-type sphincter of Oddi dysfunction (SOD) who are classified as SOD type II (biliary-type abdominal pain accompanied by hepatic enzyme elevation or common bile duct (CBD) dilation) and SOD type III (only biliary-type abdominal pain) according to Geenen-Hogan classification criteria Exclusion Criteria: Postoperative biliary calculi, benign biliary stenosis, bile duct infection, overlong residual cystic duct (> 0.5cm), biliary tumors, etc. Peptic ulcer, duodenal diverticulum Pancreatitis, pancreatic-type SOD Adhesive intestinal obstruction Postoperative irritable bowel syndrome (IBS) A history of abdominal operation or other surgery Pregnant and lactating women Use of other drugs from one week after LC to enrollment, including antispasmodic drugs, analgesics, choleretic agents, calcium ion antagonists and GI motility drugs A history of allergy to Pinaverium Bromide / Danshu Tablets
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Zhaohui Tang, MD,PhD
Phone
+86 021 25078999-7905
Email
tangzhaohui@yahoo.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Zhaohui Tang, MD,PhD
Organizational Affiliation
Xinhua Hospital,School of Medicine,Shanghai Jiao Tong University
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Zhiwei Quan, MD,PhD
Organizational Affiliation
Xinhua Hospital,School of Medicine,Shanghai Jiao Tong University
Official's Role
Study Chair
Facility Information:
Facility Name
Zhang Yong
City
Shanghai
State/Province
Shanghai
ZIP/Postal Code
200092
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Yong Zhang, MD,PhD
Phone
+86 21 25078999-7905
First Name & Middle Initial & Last Name & Degree
Yong Zhang, MD,PhD
First Name & Middle Initial & Last Name & Degree
Houbao Liu, MD,PhD
First Name & Middle Initial & Last Name & Degree
Tao Suo, MD,PhD
First Name & Middle Initial & Last Name & Degree
Jian Wang, MD,PhD
First Name & Middle Initial & Last Name & Degree
Wei Chen, MD,PhD
First Name & Middle Initial & Last Name & Degree
Yajin Chen, MD,PhD
First Name & Middle Initial & Last Name & Degree
Yunyao Xu, MD,PhD
First Name & Middle Initial & Last Name & Degree
Xiujun Cai, MD,PhD
First Name & Middle Initial & Last Name & Degree
Xiao Liang, MD,PhD
First Name & Middle Initial & Last Name & Degree
Lin Ji, MD,PhD
First Name & Middle Initial & Last Name & Degree
Jianying Lou, MD,PhD
First Name & Middle Initial & Last Name & Degree
Ji Wang, MD,PhD
First Name & Middle Initial & Last Name & Degree
Xitai Sun, MD,PhD
First Name & Middle Initial & Last Name & Degree
Xiaodong Shan, MD,PhD
First Name & Middle Initial & Last Name & Degree
Yu He, MD,PhD
First Name & Middle Initial & Last Name & Degree
Dajiang Li, MD,PhD

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
24867013
Citation
Cotton PB, Durkalski V, Romagnuolo J, Pauls Q, Fogel E, Tarnasky P, Aliperti G, Freeman M, Kozarek R, Jamidar P, Wilcox M, Serrano J, Brawman-Mintzer O, Elta G, Mauldin P, Thornhill A, Hawes R, Wood-Williams A, Orrell K, Drossman D, Robuck P. Effect of endoscopic sphincterotomy for suspected sphincter of Oddi dysfunction on pain-related disability following cholecystectomy: the EPISOD randomized clinical trial. JAMA. 2014 May;311(20):2101-9. doi: 10.1001/jama.2014.5220.
Results Reference
background
PubMed Identifier
22529689
Citation
Vitton V, Ezzedine S, Gonzalez JM, Gasmi M, Grimaud JC, Barthet M. Medical treatment for sphincter of oddi dysfunction: can it replace endoscopic sphincterotomy? World J Gastroenterol. 2012 Apr 14;18(14):1610-5. doi: 10.3748/wjg.v18.i14.1610.
Results Reference
background
PubMed Identifier
18577477
Citation
Okoro N, Patel A, Goldstein M, Narahari N, Cai Q. Ursodeoxycholic acid treatment for patients with postcholecystectomy pain and bile microlithiasis. Gastrointest Endosc. 2008 Jul;68(1):69-74. doi: 10.1016/j.gie.2007.09.046.
Results Reference
background
PubMed Identifier
20969779
Citation
Kalaitzakis E, Ambrose T, Phillips-Hughes J, Collier J, Chapman RW. Management of patients with biliary sphincter of Oddi disorder without sphincter of Oddi manometry. BMC Gastroenterol. 2010 Oct 22;10:124. doi: 10.1186/1471-230X-10-124.
Results Reference
background
PubMed Identifier
16678563
Citation
Behar J, Corazziari E, Guelrud M, Hogan W, Sherman S, Toouli J. Functional gallbladder and sphincter of oddi disorders. Gastroenterology. 2006 Apr;130(5):1498-509. doi: 10.1053/j.gastro.2005.11.063.
Results Reference
background
PubMed Identifier
16678553
Citation
Drossman DA. The functional gastrointestinal disorders and the Rome III process. Gastroenterology. 2006 Apr;130(5):1377-90. doi: 10.1053/j.gastro.2006.03.008. No abstract available.
Results Reference
background
PubMed Identifier
20665015
Citation
Hernando N, Gisler SM, Reining SC, Deliot N, Capuano P, Biber J, Murer H. NaPi-IIa interacting proteins and regulation of renal reabsorption of phosphate. Urol Res. 2010 Aug;38(4):271-6. doi: 10.1007/s00240-010-0304-3. Epub 2010 Jul 28.
Results Reference
background

Learn more about this trial

Pinaverium Bromide in Post-cholecystectomy Sphincter of Oddi Dysfunction

We'll reach out to this number within 24 hrs