Study to Evaluate the Efficacy and Safety of Hyoscine Butylbromide Tablets for the Treatment of Occasional or Recurrent Episodes of Gastric or Intestinal Spasm-like Pain or Discomfort

Abdominal Pain Clinical Trial

Official title:

A Randomized, Double-blind, Double-dummy, Active-controlled, Parallel-group, Multi-center Trial, in Contrast With Hyoscine Butylbromide Capsule 10mg, to Evaluate the Efficacy and Safety of Hyoscine Butylbromide Tablets 10 mg (20mg, 3 Times Daily, Orally) Over a Period of 3 Days for the Treatment of Occasional or Recurrent Episodes of Self-reported Gastric or Intestinal Spasm-like Pain

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT02242305
• Other study ID #: 202.838
• Status: Completed
• Phase: Phase 3
• First received: September 16, 2014
• Last updated: July 26, 2017
• Start date: November 1, 2008
• Est. completion date: July 20, 2009

Study information

• Verified date: July 2017
• Source: Boehringer Ingelheim
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

In contrast with Hyoscine Butylbromide Capsule 10mg, Study is to evaluate the efficacy and safety of Hyoscine Butylbromide tablets 10 mg (20mg, 3 times daily, orally) over a period of 3 days for the treatment of occasional or recurrent episodes of self-reported gastric or intestinal spasm-like pain or discomfort

Recruitment information / eligibility

• Status: Completed
• Enrollment: 302
• Est. completion date: July 20, 2009
• Est. primary completion date: July 20, 2009
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 70 Years

Eligibility

Inclusion Criteria:

1. Written Informed Consent given by the patient

2. Male and female patients aging from 18 to 70

3. Subjects with occasional or recurrent episodes of gastric or intestinal spasm-like pain, or discomfort, such as occur e.g. in irritable bowel syndrome, which has been present for at least 3 months

4. The pain intensity score upon screening is at least 4 cm in VAS score

Exclusion Criteria:

1. Patients with the following concomitant disease were not eligible for enrolment

• Painful gastric or intestinal spasm of organic origin such as Crohn's disease, ulcerative colitis, lactose intolerance, gastritis, ulcer. Exception: diverticulitis and mild gastritis if dominant symptom was cramp pain, but ineligible if heartburn or reflux were dominant symptoms

• Pain related with malignancy

• Patients with other severe pain states of organic origin

• Mechanical stenosis of the gastrointestinal tract, megacolon

• Urinary retention associated with mechanical stenosis of urinary tract

• Narrow-angled glaucoma

• Tachyarrhythmia

• Myasthenia gravis

• Meulengracht-Gilbert syndrome

• Known depression or known mental illness, anxiety disturbance

2. Frequent vomiting that might have prevented adequate absorption of the active ingredient after the film-coated tablet was taken

3. Patients taking the following concomitant medication are not eligible for enrolment

• Analgesics

• Spasmolytics

• Anticholinergics

• Affecting gastrointestinal motility, such as propantheline metoclopramide, cisapride, loperamide, diphenoxylate, opioid analgesics, antacids and other ulcer treatment

• Regular administration of laxatives

• Narcotics

• Antidepressant treatment or treatment with psychoactive drugs

4. Pregnancy and/or lactation or planned pregnancy

5. Known hypersensitivity to N-butylscopolammonium bromide

6. Alcohol or drug abuse

7. Simultaneous participating in another clinical trial, or discontinuing from another clinical trial before randomization (administration of study medication); moreover, in the case of screening failure or premature discontinuing from the trial, repeated enrolment is forbidden

8. Unwilling to or unable to complete the entire trial procedure according to the protocol

9. In investigator's opinion, the patient was not proper for the trial

Related Conditions & MeSH terms

• Abdominal Pain

Intervention

Drug:
• Hyoscine Butylbromide - Tablet

• Hyoscine Butylbromide - Capsule

• Placebo

Locations

Country	Name	City	State
n/a

Sponsors (1)

Lead Sponsor	Collaborator
Boehringer Ingelheim

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Change of the Mean Pain Intensity Score Measured on a Visual Analogue Scale (VAS) Within 3 Days (and Within 1 Day) - ANCOVA	The endpoint presents change of the mean Visual Analogue Scale (VAS) of pain intensity score, recorded daily by the patient in the evening in his/her patient diary describing pain intensity during the previous 24 hours, from the baseline pain intensity. The baseline pain intensity was the pain intensity of first episode on Day 1 after randomization before taking study medication. The mean VAS pain intensity score was calculated for the 3-day treatment period. A VAS for describing the pain intensity was used (VAS: maximum score of 10 cm, the score from 0 - 10 cm reaching from "no pain" to "the most severe pain imaginable").	3 days (1 day)
Secondary	Change of the Pain Frequency Assessed on 4-stage Verbal Rating Scale (VRS)	The endpoint presents frequency improvement, change of the pain frequency from baseline pain frequency for each of Day 1 - 3. Baseline pain frequency meant the pain frequency before randomization on visit 1. VRS score of Day 3 change from baseline was calculated. A retrospective assessment was entered by the patient in the patient diary, again once daily in the evening, of the pain frequency over the preceding 24 hour period. This was based on a 4-stage Verbal Rating Scale (VRS) with the following scores to the question: "How many times have the spasm-like pains occurred today?" 0 = not at all, 1 = 1-2 times, 2 = 3-5 times, 3 = more than 5 times.	Up to 3 days.
Secondary	Global Assessment of Efficacy by Patient on 4-point Scale	The endpoint presents global assessment of efficacy: by the patient after 3 days of treatment using a 4-point rating scale (good, satisfactory, not satisfactory, and bad).	Post 3 days of treatment.
Secondary	Number of Patients With Adverse Events	The endpoint presents number of patients with Adverse Events (AEs). Subjects were required to report spontaneously any AEs as well as the time of onset, end and intensity of these events. Specific questions were asked wherever required or useful to more precisely describe an AE. An Adverse Event was termed serious when one of the following applied: death, directly lifethreatening, continuous or severe impairment, in-patient treatment or prolonging of hospitalization, congenital deformity and other similar medical criteria.	Up to 3 days.
Secondary	Global Assessment of Tolerability by Investigator on a 4-point Scale	The endpoint presents global assessment of tolerability by subject on a 4-point scale. Global assessment of tolerability regarding all episodes treated by the subject after 3 days of treatment (good, satisfactory, not satisfactory, bad).	Day 3.
Secondary	Number of Subjects With Clinical Relevant Abnormalities for Laboratory, Vital Signs, ElectroCardioGram (ECG) and Physical Examination	Number of patients with findings in clinical relevant abnormalities for laboratory, vital signs, ElectroCardioGram (ECG) and physical examination. Relevant findings or worsening of baseline conditions were reported as Adverse Events (AEs).	Up to 3 days.
Secondary	Percentage of Event for Time to Therapeutic Effect	This outcome measure presents percentage of event for time to therapeutic effect defined as the time that the first VAS reduction occurred.	From time of the first dose to the time that the first VAS reduction occurred, up to 180 minutes after the first dose on Day 1.

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