Longitudinal Study of Patients With Opioid-Induced Constipation
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.
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
- Enrollment
- 520 participants
Conditions and interventions
Conditions
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.