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Clinical trialNCT01928953CompletedObservational

Longitudinal Study of Patients With Opioid-Induced Constipation

SponsorAstraZenecaEnrollment520Patients With Opioid Induced Constipation
View the registry record on ClinicalTrials.gov

Summary

The lay summary the sponsor registered on ClinicalTrials.gov.

This prospective hybrid longitudinal study was conducted in the United States (US), Canada, the United Kingdom (UK), and Germany. To obtain the most complete and comprehensive understanding of the burden of opioid-induced constipation (OIC) in these countries, this study used a combination of web-based, longitudinal patient survey, retrospective data abstraction from medical records, and a prospective physician survey. The primary objective of this study was to estimate the rate of inadequate response to laxatives (LIR), which was defined as having sufficient laxative use (at least one laxative use ≥ four times per reference period), and inadequate response (defined as fewer than three bowel movements (BMs) OR at least one of the following symptoms on the Patient Assessment of Constipation Symptoms (PAC-SYM) measure scored as moderate, severe or very severe: BMs too hard, straining to have a BM, feeling like you didn't "finish" a BM, and feeling like you had to pass a BM but could not), in a cohort of non-cancer pain and cancer pain (separately) participants with OIC, by country and overall. The secondary study objectives are as follows: 1. To estimate the rate of LIR for two subgroups: 1xLIR and 2xLIR. 1xLIR was defined as use of at least one laxative agent ≥ 4 times in the reference period while 2xLIR was defined as the use of at least two laxative agents, each used ≥ 4 times in the reference period; 2. To describe the baseline demographic and clinical characteristics, including prior health status, comorbidities, constipation-related GI symptoms, and concomitant medications of patients with OIC; 3. To describe drug utilization and self-management of OIC; 4. To describe the pre-index and post-index healthcare resource utilization and estimate costs associated with the diagnosis, treatment, and general management of OIC (including laxative use) and events attributed to OIC, including both direct and indirect costs; 5. To describe patient-reported impact of OIC on health-related quality of life, productivity, and pain management; 6. To describe patient-reported treatment satisfaction with laxative use; and 7. To describe physician-reported awareness of OIC and symptoms and understanding of patient-reported impact of OIC.

Investigators

The overall officials registered on this study. Names that resolve to a findmyKOL profile link to it; the rest are shown as registered.

A profile link is shown only when the registered name resolves to a person record with a confident, namesake-checked match; ambiguous names stay unlinked.

Sites

30 registered facilities, with the per-site recruitment status where the registry publishes one. ClinicalTrials.gov does not publish per-site enrollment counts.

Canada
  • University of Calgary

    Calgary, Alberta, Canada

  • Paradise Medical Clinic

    Paradise, Newfoundland and Labrador, Canada

  • Aviva Clinical Trial Group Inc.

    Burlington, Ontario, Canada

  • Skds Research Inc.

    Newmarket, Ontario, Canada

  • Taunton Health Centre

    Oshawa, Ontario, Canada

  • Pro-Recherche

    Saint Romuald, Quebec, Canada

United States
  • Alliance Clinical Research

    Birmingham, Alabama, United States

  • Horizon Research Group, Inc

    Mobile, Alabama, United States

  • Hope Research Institute

    Phoenix, Arizona, United States

  • Advanced Rx Clinical Research

    Artelia, California, United States

  • Triwest Research Associates, Llc

    El Cajon, California, United States

  • Akkiance Research Centers

    Laguna Hills, California, United States

  • Primecare Clinical Research

    Lajuna Hills, California, United States

  • Samaritan Center for Medical Research

    Los Gatos, California, United States

  • Precision Research Institute, Llc

    San Diego, California, United States

  • Southeast Clinical Research, Llc

    Jacksonville, Florida, United States

  • Physician Care Clinical Research, Llc

    Sarasota, Florida, United States

  • Soth Miami Clinical Research

    South Miami, Florida, United States

  • Chicago Anesthesia Pain Specialists

    Chicago, Illinois, United States

  • Activmed Practices & Research

    Newington, New Hampshire, United States

  • Atco Medical Associates, P.C.

    Atco, New Jersey, United States

  • Digiovanna Institute for Medical Education and Research

    North Massapequa, New York, United States

  • Gaffnew Health Services

    Charlotte, North Carolina, United States

  • Clinical Inquest Center Ltd

    Beavercreek, Ohio, United States

  • Ohio Clinical Research Partners, Llc

    Canton, Ohio, United States

  • Clinical Inquest Center, Ltd.

    Dayton, Ohio, United States

  • Npc Research

    Oklahoma City, Oklahoma, United States

  • Pain Research of Charleston

    Charleston, South Carolina, United States

  • Family Medicine of Sayebrook

    Myrtle Beach, South Carolina, United States

  • Highland Clinical Research

    Salt Lake City, Utah, United States

Site investigator names are published by ClinicalTrials.gov only while a study recruits, so completed studies list sites without them.

Drugs studied

No drug or biological interventions are in our data for this study. It may test a procedure, device or behavioral intervention, or the intervention list isn't in our current snapshot. See the registry record ↗. Why? →

Registration & key dates

Registry attributes as recorded on the ClinicalTrials.gov study record.

Start
31 Oct 2012
Primary completion
31 Dec 2014
Completion
31 Dec 2014
Last update posted
8 Jul 2015
Registered enrollment
520
Registry id
NCT01928953

Source: ClinicalTrials.gov, via the CTTI AACT database, data as of 24 Aug 2026. Registry facts are shown as registered by the study sponsor; findmyKOL does not interpret them.