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Buscopan Versus Acetaminophen for Acute Abdominal Pain in Children

Primary Purpose

Abdomen, Acute, Children

Status
Completed
Phase
Phase 3
Locations
Canada
Study Type
Interventional
Intervention
Acetaminophen, Analgesics, Non-Narcotic
Hyoscine butylbromide, Analgesics, Non-Narcotic
Sponsored by
Lawson Health Research Institute
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Abdomen, Acute

Eligibility Criteria

8 Years - 17 Years (Child)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • All children aged 8-17 years presenting to the paediatric ED with:

    1. A chief complaint of colicky abdominal pain AND
    2. Pain score of at least 4/10 on the Faces Pain Scale - Revised AND
    3. A presumed non-surgical etiology

Exclusion Criteria:

  1. Prior abdominal surgery
  2. Concomitant use of other anticholinergic medication including but not limited to tricyclic antidepressants, antihistamines, benztropine mesylate
  3. Signs and symptoms consistent with a bowel obstruction
  4. Peritoneal signs
  5. Suspected previous hypersensitivity reaction to either acetaminophen or HBB
  6. Suspected appendicitis
  7. History of abdominal trauma within 48 hours of presentation
  8. Unstable vital signs
  9. History of bowel obstruction
  10. Myasthenia gravis
  11. Fever (aural temperature > 38.2 C)
  12. Chronic liver disease
  13. Persistent vomiting despite administration of oral anti-emetic
  14. Symptoms and signs consistent with a urinary tract infection
  15. Symptoms and signs consistent with a toxin ingestion
  16. Symptoms and signs consistent with gynecological or gonadal pathology
  17. Symptoms and signs consistent with vasoocclusive crisis in a patient with a hemoglobinopathy

Sites / Locations

  • London Health Sciences Centre

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Hyoscine butylbromide

Acetaminophen

Arm Description

Hyoscine butylbromide 10mg oral single dose

Acetaminophen 15mg/kg oral single dose (maximum 1000mg)

Outcomes

Primary Outcome Measures

Analgesic Efficacy
Pain severity on a 100 mm Visual Analog Scale (VAS)

Secondary Outcome Measures

Analgesic Efficacy
Pain severity on Faces Pain Scale - Revised and VAS
Analgesic Efficacy
Pain severity on Faces Pain Scale - Revised and VAS
Analgesic Efficacy
Pain severity on Faces Pain Scale - Revised and VAS
Analgesic Efficacy
Pain severity on Faces Pain Scale - Revised and VAS
Need for Rescue Analgesia
Frequency of rescue analgesia
Time to Analgesia
Time to Achieve 20% Reduction in Faces Pain Score - Revised from time 0
Adequacy of Sedation
Proportion of participants that achieve a pain score < 30 mm on the VAS
Adverse Effects
Frequency of Adverse Effects
Caregiver Satisfaction
Satisfaction scores on 5-Item Likert Scale
Return visits
Proportion of participants with return visits for surgical pathology

Full Information

First Posted
October 13, 2015
Last Updated
April 30, 2019
Sponsor
Lawson Health Research Institute
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1. Study Identification

Unique Protocol Identification Number
NCT02582307
Brief Title
Buscopan Versus Acetaminophen for Acute Abdominal Pain in Children
Official Title
Hyoscine Hydrobromide (Buscopan) Versus Acetaminophen for Acute Abdominal Pain in Children: A Randomized Controlled Trial
Study Type
Interventional

2. Study Status

Record Verification Date
April 2019
Overall Recruitment Status
Completed
Study Start Date
March 20, 2017 (Actual)
Primary Completion Date
December 3, 2018 (Actual)
Study Completion Date
February 22, 2019 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Lawson Health Research Institute

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
There is ample evidence that pain in children is under recognized and under treated. This is especially true for acute abdominal pain, a common complaint in the paediatric emergency department. Clinicians often fear that analgesia will obscure the diagnosis of a potentially surgical condition. As a result, acute abdominal pain goes untreated in many children, as there is no standard of care. Hyoscine N-butylbromide (Buscopan) has been used successfully in adults and children for pain associated with urinary tract infections and kidney stones for over 60 years. However, no study has explored its usefulness in relieving acute abdominal pain in children. The objectives of this study are to investigate to what degree Buscopan is effective in relieving abdominal pain in children compared to acetaminophen.
Detailed Description
Acute abdominal pain is a common complaint among paediatric patients visiting the emergency department (ED). Functional abdominal pain is not associated with any surgical or infectious etiology and is a frequent cause of painful abdominal cramps. Although functional abdominal pain is not life-threatening, it has significant impact on quality of life, functional outcomes, and patient satisfaction. It is a major source of school and work absence, loss of sleep, and extracurricular impairment. Despite this, analgesia has traditionally been withheld from patients with acute abdominal pain. The reasons behind this are likely two-fold. First, there is good evidence that clinicians fear that analgesia will mask signs of an underlying surgical pathology such as appendicitis. There is no current published literature that supports this practice. In fact, recent evidence has found that providing analgesia to children does not obscure signs of an acute surgical abdomen nor lead to clinically significant differences in negative outcomes. Second, there is no standard of care specifying the best analgesic options for treating abdominal pain in children in the post-codeine era. Although acetaminophen, ibuprofen, ketorolac, buscopan, and almagel/viscous lidocaine are frequently used agents in the ED, evidence for their benefit in children with functional abdominal pain is lacking. As a predictable result, most patients who present with abdominal pain fail to experience pain relief at discharge. The importance of providing optimal pain treatment is echoed by several national and international level policy statements. In addition to the World Health Organization (WHO)'s mandate that adequate pain treatment should be a fundamental human right, the American Academy of Pediatrics (AAP) has reaffirmed its position that adequate analgesia be provided for children. Furthermore, literature supports that providing analgesia improves patient care, caregiver satisfaction, and the therapeutic relationship. Antispasmodics are commonly used agents to treat abdominal cramping. Hyoscine butylbromide (HBB), trade name: Buscopan, is an anticholinergic agent that when orally administered, does not cross the blood brain barrier and has minimal systemic absorption. Therefore, it inhibits bowel motility without central nervous system or peripheral side effects. This antispasmodic has been used in clinical practice for over 60 years and specifically has been on the market since 1952 for the treatment of abdominal cramps. It is widely available around the world as both a prescription drug and an over the counter medication in many industrialized countries. It has also been used safely in neonates and children. As hyoscine butylbromide is barely absorbed, it is generally well tolerated. In the two large-scale studies of almost 1200 patients that compared HBB with placebo (and paracetamol), there was no significant difference in adverse events between the two groups, including those commonly associated with anticholinergics, such as nausea, constipation, dry mouth, blurred vision, tachycardia and urinary retention. Moreover, these adverse events not only occurred at a low incidence (less than or equal to 1.5%) but were also usually mild and self-limiting. In abdominal cramping and pain associated with irritable bowel syndrome, systematic reviews have had conflicting results with regards to analgesic efficacy, primarily because of small sample sizes and less rigorous designs. Muller-Krampe et al. conducted a prospective cohort of over 200 children with both acute and chronic abdominal spasms and compared the effectiveness of oral HBB 10 mg to a homeopathic preparation. HBB demonstrated comparative improvements to the homeopathic preparation with respect to pain, sleep disturbance, eating and drinking, and crying. Over 90% of patients in both groups reported good tolerability and there were no adverse events. Although HBB is used widely for abdominal pain in children and anecdotal evidence suggests it is efficacious, no paediatric clinical trial to date has explored its efficacy in the ED setting. The investigators hypothesize that HBB will have superior efficacy to the most commonly used agent, acetaminophen for acute abdominal pain in children. If HBB is found to be an effective analgesic in children with acute abdominal pain, it could provide a therapeutic option for a common, painful condition for which there is currently very little to offer.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Abdomen, Acute, Children

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
236 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Hyoscine butylbromide
Arm Type
Experimental
Arm Description
Hyoscine butylbromide 10mg oral single dose
Arm Title
Acetaminophen
Arm Type
Active Comparator
Arm Description
Acetaminophen 15mg/kg oral single dose (maximum 1000mg)
Intervention Type
Drug
Intervention Name(s)
Acetaminophen, Analgesics, Non-Narcotic
Other Intervention Name(s)
Tylenol
Intervention Description
Oral single dose
Intervention Type
Drug
Intervention Name(s)
Hyoscine butylbromide, Analgesics, Non-Narcotic
Other Intervention Name(s)
Buscopan
Intervention Description
Oral single dose
Primary Outcome Measure Information:
Title
Analgesic Efficacy
Description
Pain severity on a 100 mm Visual Analog Scale (VAS)
Time Frame
80 minutes post-intervention
Secondary Outcome Measure Information:
Title
Analgesic Efficacy
Description
Pain severity on Faces Pain Scale - Revised and VAS
Time Frame
15 minutes post-intervention
Title
Analgesic Efficacy
Description
Pain severity on Faces Pain Scale - Revised and VAS
Time Frame
30 minutes post-intervention
Title
Analgesic Efficacy
Description
Pain severity on Faces Pain Scale - Revised and VAS
Time Frame
45 minutes post-intervention
Title
Analgesic Efficacy
Description
Pain severity on Faces Pain Scale - Revised and VAS
Time Frame
60 minutes post-intervention
Title
Need for Rescue Analgesia
Description
Frequency of rescue analgesia
Time Frame
80 minutes post-intervention
Title
Time to Analgesia
Description
Time to Achieve 20% Reduction in Faces Pain Score - Revised from time 0
Time Frame
80 minutes post-intervention
Title
Adequacy of Sedation
Description
Proportion of participants that achieve a pain score < 30 mm on the VAS
Time Frame
80 minutes post-intervention
Title
Adverse Effects
Description
Frequency of Adverse Effects
Time Frame
80 minutes post-intervention
Title
Caregiver Satisfaction
Description
Satisfaction scores on 5-Item Likert Scale
Time Frame
80 minutes post-intervention
Title
Return visits
Description
Proportion of participants with return visits for surgical pathology
Time Frame
72 hours post discharge

10. Eligibility

Sex
All
Minimum Age & Unit of Time
8 Years
Maximum Age & Unit of Time
17 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: All children aged 8-17 years presenting to the paediatric ED with: A chief complaint of colicky abdominal pain AND Pain score of at least 4/10 on the Faces Pain Scale - Revised AND A presumed non-surgical etiology Exclusion Criteria: Prior abdominal surgery Concomitant use of other anticholinergic medication including but not limited to tricyclic antidepressants, antihistamines, benztropine mesylate Signs and symptoms consistent with a bowel obstruction Peritoneal signs Suspected previous hypersensitivity reaction to either acetaminophen or HBB Suspected appendicitis History of abdominal trauma within 48 hours of presentation Unstable vital signs History of bowel obstruction Myasthenia gravis Fever (aural temperature > 38.2 C) Chronic liver disease Persistent vomiting despite administration of oral anti-emetic Symptoms and signs consistent with a urinary tract infection Symptoms and signs consistent with a toxin ingestion Symptoms and signs consistent with gynecological or gonadal pathology Symptoms and signs consistent with vasoocclusive crisis in a patient with a hemoglobinopathy
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Naveen Poonai, MD
Organizational Affiliation
Western University Health
Official's Role
Principal Investigator
Facility Information:
Facility Name
London Health Sciences Centre
City
London
State/Province
Ontario
ZIP/Postal Code
N6A5W9
Country
Canada

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
33257343
Citation
Poonai N, Kumar K, Coriolano K, Thompson G, Brahmbhatt S, Dzongowski E, Stevens H, Gupta P, Miller M, Elsie S, Ashok D, Joubert G, Lim R, Butter A, Ali S. Hyoscine butylbromide versus acetaminophen for nonspecific colicky abdominal pain in children: a randomized controlled trial. CMAJ. 2020 Nov 30;192(48):E1612-E1619. doi: 10.1503/cmaj.201055.
Results Reference
derived

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Buscopan Versus Acetaminophen for Acute Abdominal Pain in Children

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