Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

COMPLETED Phase 2

(Hyoscine Butylbromide) for Abdominal Pain Associated With Cramping on Demand Basis

NCT00932737 · View on ClinicalTrials.gov ↗

Study Summary

The primary objective of this pilot study is to assess effects of Hyoscine Butylbromide (HBB) 20 mg in comparison to placebo, when used as needed, as measured by the subject's assessment of intensity of abdominal pain associated with cramping (APC) in the treatment of two episodes.

Conditions Studied

Interventions

  • DRUG Placebo
  • DRUG HBB 20 mg

Study Locations (19)

Florida

  • 202.839.01003 Boehringer Ingelheim Investigational Site — Hollywood
  • 202.839.01001 Boehringer Ingelheim Investigational Site — Jupiter
  • 202.839.01002 Boehringer Ingelheim Investigational Site — Jupiter

Oklahoma

  • 202.839.01021 Boehringer Ingelheim Investigational Site — Norman
  • 202.839.01010 Boehringer Ingelheim Investigational Site — Oklahoma City

Texas

  • 202.839.01006 Boehringer Ingelheim Investigational Site — San Antonio
  • 202.839.01012 Boehringer Ingelheim Investigational Site — San Antonio

California

  • 202.839.01014 Boehringer Ingelheim Investigational Site — Westlake Village

Illinois

  • 202.839.01017 Boehringer Ingelheim Investigational Site — Rockford

Indiana

  • 202.839.01005 Boehringer Ingelheim Investigational Site — Indianapolis

Maryland

  • 202.839.01019 Boehringer Ingelheim Investigational Site — Chevy Chase

Massachusetts

  • 202.839.01009 Boehringer Ingelheim Investigational Site — Boston

Trial Details

FieldValue
Enrollment Target 197 participants
Start Date 2009-06-09
Est. Completion 2010-02-08
Phase Phase 2

Sponsor

Boehringer Ingelheim

203 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT00932737

The ClinicalTrials.gov registry entry for NCT00932737 describes a study currently listed as completed. It is categorized as Phase 2, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 197 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Boehringer Ingelheim, which has 203 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 1 condition, with Abdominal Pain appearing as the primary indexed condition, and to 2 interventions — of which Placebo is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT00932737 reports 19 study locations spanning 15 distinct geographic areas — top geographies include Florida, Oklahoma, Texas. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT00932737 about?

NCT00932737 is a clinical study titled "(Hyoscine Butylbromide) for Abdominal Pain Associated With Cramping on Demand Basis". The primary objective of this pilot study is to assess effects of Hyoscine Butylbromide (HBB) 20 mg in comparison to placebo, when used as needed, as measured by the subject's assessment of intensity of abdominal pain associated with cramping (APC) in the treatment of two episodes.

What is the current status of trial NCT00932737?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 197 participants. The study started on 2009-06-09. Estimated completion is 2010-02-08.

What conditions does trial NCT00932737 study?

This clinical trial studies the following conditions: Abdominal Pain. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT00932737?

The interventions under investigation include: Placebo (DRUG), HBB 20 mg (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT00932737?

This trial is sponsored by Boehringer Ingelheim, which has 203 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT00932737 being conducted?

This trial has 19 study locations across California, Florida, Illinois, Indiana, Maryland. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial