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Abdomen, AcutePhase 3NCT02582307

Buscopan Versus Acetaminophen for Acute Abdominal Pain in Children

A Phase 3 study testing Acetaminophen, Analgesics, Non-Narcotic and Hyoscine butylbromide, Analgesics, Non-Narcotic in people with Abdomen, Acute and Children, run by London Health Sciences Centre Research Institute OR Lawson Research Institute of St. Joseph's at 1 site in Canada.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial 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. Read more about this study

Who is it for?
Ages 8 to 17 years
Conditions the study is for
Abdomen, Acute, Children
What is being tested?
Acetaminophen, Analgesics, Non-Narcotic and Hyoscine butylbromide, Analgesics, Non-Narcotic
Type of treatment
Pill or oral medicine
Could I receive a placebo?
No, everyone receives an active treatment
How many people
236 participants
Where
1 siteCanada
Study dates
20 Mar 2017to 22 Feb 2019
Phase
Phase 3
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 8 to 17 years
  • All sexes
  • No healthy volunteers
  • Child

Who may be able to join

  • 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

Who cannot join

  • 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
Show all 17Show fewer
  • 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

Trial locations and contacts

1 site in 1 country.

Canada1 site
  • London Health Sciences Centre

    London, Ontario, N6A5W9

Other trials in Canada

About this study

Official title: Hyoscine Hydrobromide (Buscopan) Versus Acetaminophen for Acute Abdominal Pain in Children: A Randomized Controlled Trial

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.

Read the 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.

Being tested
Acetaminophen, Analgesics, Non-Narcotic, Hyoscine butylbromide, Analgesics, Non-Narcotic
Medical subject headings
Abdomen, Acute

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Acetaminophen, Analgesics, Non-NarcoticDrug

    Also called Tylenol

    Oral single dose

  • Hyoscine butylbromide, Analgesics, Non-NarcoticDrug

    Also called Buscopan

    Oral single dose

Study groups in NCT02582307
Study groupRoleWhat they receive
Hyoscine butylbromideExperimentalHyoscine butylbromide 10mg oral single dose
Receives: Drug: Hyoscine butylbromide, Analgesics, Non-Narcotic
AcetaminophenActive comparatorAcetaminophen 15mg/kg oral single dose (maximum 1000mg)
Receives: Drug: Acetaminophen, Analgesics, Non-Narcotic

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Analgesic Efficacy

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

    Measured: 80 minutes post-intervention

Secondary outcomes (10)
  1. Analgesic Efficacy

    Pain severity on Faces Pain Scale - Revised and VAS

    Measured: 15 minutes post-intervention

  2. Analgesic Efficacy

    Pain severity on Faces Pain Scale - Revised and VAS

    Measured: 30 minutes post-intervention

  3. Analgesic Efficacy

    Pain severity on Faces Pain Scale - Revised and VAS

    Measured: 45 minutes post-intervention

  4. Analgesic Efficacy

    Pain severity on Faces Pain Scale - Revised and VAS

    Measured: 60 minutes post-intervention

  5. Need for Rescue Analgesia

    Frequency of rescue analgesia

    Measured: 80 minutes post-intervention

  6. Time to Analgesia

    Time to Achieve 20% Reduction in Faces Pain Score - Revised from time 0

    Measured: 80 minutes post-intervention

  7. Adequacy of Sedation

    Proportion of participants that achieve a pain score < 30 mm on the VAS

    Measured: 80 minutes post-intervention

  8. Adverse Effects

    Frequency of Adverse Effects

    Measured: 80 minutes post-intervention

  9. Caregiver Satisfaction

    Satisfaction scores on 5-Item Likert Scale

    Measured: 80 minutes post-intervention

  10. Return visits

    Proportion of participants with return visits for surgical pathology

    Measured: 72 hours post discharge

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted21 Oct 2015 (estimated)
  2. Study start20 Mar 2017
  3. Primary completion3 Dec 2018
  4. Study completion22 Feb 2019

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase 3
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Masking
Quadruple blind
Who is masked
Participant, Care provider, Investigator, Outcomes assessor
Enrolment
236 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT02582307
Sponsor's protocol ID
107243
Status last verified
Apr 2019
First submitted
13 Oct 2015
Last updated
2 May 2019
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Publications

  • 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.

    PubMed 33257343

Questions about this trial

What is this clinical trial studying?

A Phase 3 study testing Acetaminophen, Analgesics, Non-Narcotic and Hyoscine butylbromide, Analgesics, Non-Narcotic in people with Abdomen, Acute and Children, run by London Health Sciences Centre Research Institute OR Lawson Research Institute of St. Joseph's at 1 site in Canada.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 4 inclusion and 17 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 2 May 2019. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Canada. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

What does this phase mean?

Phase 3 studies compare the treatment with the current standard treatment or a placebo in a large group, to confirm how well it works and watch for side effects.

Not every study follows the same path, and some studies (observational studies, device studies) have no phase.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Analgesic Efficacy (time frame: 80 minutes post-intervention). It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT02582307, which also lists 1 linked publication.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 2 May 2019.

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