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Completed No phase listed Observational

Longitudinal Study of Patients With Opioid-Induced Constipation

ClinicalTrials.gov ID: NCT01928953

Public ClinicalTrials.gov record NCT01928953. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Sep 7, 2026, 3:51 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

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.

Study identification

NCT ID
NCT01928953
Recruitment status
Completed
Study type
Observational
Phase
Not listed
Lead sponsor
AstraZeneca
Industry
Enrollment
520 participants

Conditions and interventions

Interventions

Not listed

Eligibility (public fields only)

Age range
18 Years to 85 Years
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Sep 30, 2012
Primary completion
Nov 30, 2014
Completion
Nov 30, 2014
Last update posted
Jul 7, 2015

2012 – 2014

United States locations

U.S. sites
24
U.S. states
13
U.S. cities
24
Facility City State ZIP Site status
Alliance Clinical Research Birmingham Alabama
Horizon Research Group, Inc Mobile Alabama
HOPE Research Institute Phoenix Arizona
Advanced Rx Clinical Research Artelia California
TriWest Research Associates, LLC El Cajon California
Akkiance Research Centers Laguna Hills California
Primecare Clinical Research Lajuna Hills California
Samaritan Center for Medical Research Los Gatos California
Precision Research Institute, LLC San Diego California
Southeast Clinical Research, LLC Jacksonville Florida
Physician Care Clinical Research, LLC Sarasota Florida
Soth Miami Clinical Research South Miami Florida
Chicago Anesthesia Pain Specialists Chicago Illinois
ActivMed Practices & Research Newington New Hampshire
Atco Medical Associates, P.C. Atco New Jersey
DiGiovanna Institute for medical Education and Research North Massapequa New York
Gaffnew Health Services Charlotte North Carolina
Clinical Inquest Center LTD Beavercreek Ohio
Ohio Clinical Research Partners, LLC Canton Ohio
Clinical Inquest Center, Ltd. Dayton Ohio
NPC Research Oklahoma City Oklahoma
Pain Research of Charleston Charleston South Carolina
Family Medicine of SayeBrook Myrtle Beach South Carolina
Highland Clinical Research Salt Lake City Utah

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 6 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01928953, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Jul 7, 2015 · Synced Sep 7, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01928953 live on ClinicalTrials.gov.

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