Buscopan Versus Acetaminophen for Acute Abdominal Pain in Children
Hyoscine Hydrobromide (Buscopan) Versus Acetaminophen for Acute Abdominal Pain in Children: A Randomized Controlled Trial
Study Overview
Status
Status
Conditions
Conditions
Intervention / Treatment
Intervention / Treatment
Detailed Description
Study Type
Study Type
Enrollment (Actual)
Enrollment
Phase
Phase
- Phase 3
Contacts and Locations
Study Locations
-
-
Ontario
-
London, Ontario, Canada, N6A5W9
- London Health Sciences Centre
-
-
Participation Criteria
Eligibility Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
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
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Quadruple
Number of Arms
Arms and Interventions
Participant Group / ArmParticipant Group / Arm |
Intervention / TreatmentIntervention / Treatment |
|---|---|
|
Experimental: Hyoscine butylbromide
Hyoscine butylbromide 10mg oral single dose
|
Oral single dose
Other Names:
|
|
Active Comparator: Acetaminophen
Acetaminophen 15mg/kg oral single dose (maximum 1000mg)
|
Oral single dose
Other Names:
|
What is the study measuring?
Primary Outcome Measures
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Analgesic Efficacy
Time Frame: 80 minutes post-intervention
|
Pain severity on a 100 mm Visual Analog Scale (VAS)
|
80 minutes post-intervention
|
Secondary Outcome Measures
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Analgesic Efficacy
Time Frame: 15 minutes post-intervention
|
Pain severity on Faces Pain Scale - Revised and VAS
|
15 minutes post-intervention
|
|
Analgesic Efficacy
Time Frame: 30 minutes post-intervention
|
Pain severity on Faces Pain Scale - Revised and VAS
|
30 minutes post-intervention
|
|
Analgesic Efficacy
Time Frame: 45 minutes post-intervention
|
Pain severity on Faces Pain Scale - Revised and VAS
|
45 minutes post-intervention
|
|
Analgesic Efficacy
Time Frame: 60 minutes post-intervention
|
Pain severity on Faces Pain Scale - Revised and VAS
|
60 minutes post-intervention
|
|
Need for Rescue Analgesia
Time Frame: 80 minutes post-intervention
|
Frequency of rescue analgesia
|
80 minutes post-intervention
|
|
Time to Analgesia
Time Frame: 80 minutes post-intervention
|
Time to Achieve 20% Reduction in Faces Pain Score - Revised from time 0
|
80 minutes post-intervention
|
|
Adequacy of Sedation
Time Frame: 80 minutes post-intervention
|
Proportion of participants that achieve a pain score < 30 mm on the VAS
|
80 minutes post-intervention
|
|
Adverse Effects
Time Frame: 80 minutes post-intervention
|
Frequency of Adverse Effects
|
80 minutes post-intervention
|
|
Caregiver Satisfaction
Time Frame: 80 minutes post-intervention
|
Satisfaction scores on 5-Item Likert Scale
|
80 minutes post-intervention
|
|
Return visits
Time Frame: 72 hours post discharge
|
Proportion of participants with return visits for surgical pathology
|
72 hours post discharge
|
Collaborators and Investigators
Sponsor
Sponsor
Investigators
Investigators
- Principal Investigator: Naveen Poonai, MD, Western University Health
Publications and helpful links
Study record dates
Study Major Dates
Study Start (Actual)
Study Start
Primary Completion (Actual)
Primary Completion
Study Completion (Actual)
Study Completion
Study Registration Dates
First Submitted
First Submitted
First Submitted That Met QC Criteria
First Submitted That Met QC Criteria
First Posted (Estimate)
First Posted
Study Record Updates
Last Update Posted (Actual)
Last Update Posted
Last Update Submitted That Met QC Criteria
Last Update Submitted That Met QC Criteria
Last Verified
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
- Pain
- Neurologic Manifestations
- Signs and Symptoms, Digestive
- Abdominal Pain
- Abdomen, Acute
- Physiological Effects of Drugs
- Neurotransmitter Agents
- Molecular Mechanisms of Pharmacological Action
- Parasympatholytics
- Autonomic Agents
- Peripheral Nervous System Agents
- Muscarinic Antagonists
- Cholinergic Antagonists
- Cholinergic Agents
- Sensory System Agents
- Antipyretics
- Antiemetics
- Gastrointestinal Agents
- Adjuvants, Anesthesia
- Mydriatics
- Acetaminophen
- Analgesics
- Scopolamine
- Butylscopolammonium Bromide
- Analgesics, Non-Narcotic
Other Study ID Numbers
Other Study ID Numbers
- 107243
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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