- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06835335
Opioid Prescribing in the Emergency Department for Sickle Cell Disease (DOPED-SCD)
January 21, 2026 updated by: Centre Hospitalier Universitaire de Nīmes
Differential Opioid Prescribing in the Emergency Department for Patients With Sickle Cell Disease: a Vignette-based International Randomised Trial.
This study consists of a clinical vignette presented to emergency physicians asking them what they would prescribe to a patient with acute abdominal pain.
Study Overview
Status
Completed
Intervention / Treatment
Study Type
Observational
Enrollment (Actual)
1063
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Occitanie
-
Nîmes, Occitanie, France, 30900
- CHU de Nîmes
-
-
-
-
Manchester
-
Manchester, Manchester, United Kingdom, M139WL
- Manchester University NHS FT
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
No
Sampling Method
Non-Probability Sample
Study Population
Population will consist in emergency medicine resident and physician, speaking French or English, in European countries.
The population will be recruited with the use of professional networks and social medias
Description
Inclusion Criteria:
- Being a emergency physician
Exclusion Criteria:
- Working outside of Europe.
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
Non-black man
the case will present a non black man
|
The intervention consisted of a randomized questionnaire presenting a clinical case of a patient suffering from severe abdominal pain.
The control case was "As an emergency physician in an adult emergency department, you are presented with the following patient: The patient is a 39-year-old non-smoking male/female with a history of Meniere's disease and an allergy to Bactrim.
He/she presents with abdominal pain that began abruptly 2 hours ago and has persisted despite taking NEFOPAM 45 minutes ago.
This is his first episode.
His/her vital signs are blood pressure 140/66, heart rate 91, pulse ox 97%, temperature 36.8°C.
He/she rates his/her pain as 8/10 without any analgesic position.
On clinical examination he/she presents with localized epigastric tenderness.
The rest of the abdomen is soft, painless and depressed.
There are hydro-aeriform noises.
No diarrhea or vomiting.
The rest of the clinical examination showed no abnormalities.".
In the intervention case, patient had history of S
|
|
Black man
the case will present a non black man
|
The intervention consisted of a randomized questionnaire presenting a clinical case of a patient suffering from severe abdominal pain.
The control case was "As an emergency physician in an adult emergency department, you are presented with the following patient: The patient is a 39-year-old non-smoking male/female with a history of Meniere's disease and an allergy to Bactrim.
He/she presents with abdominal pain that began abruptly 2 hours ago and has persisted despite taking NEFOPAM 45 minutes ago.
This is his first episode.
His/her vital signs are blood pressure 140/66, heart rate 91, pulse ox 97%, temperature 36.8°C.
He/she rates his/her pain as 8/10 without any analgesic position.
On clinical examination he/she presents with localized epigastric tenderness.
The rest of the abdomen is soft, painless and depressed.
There are hydro-aeriform noises.
No diarrhea or vomiting.
The rest of the clinical examination showed no abnormalities.".
In the intervention case, patient had history of S
|
|
non-black woman
the case will present a non black woman
|
The intervention consisted of a randomized questionnaire presenting a clinical case of a patient suffering from severe abdominal pain.
The control case was "As an emergency physician in an adult emergency department, you are presented with the following patient: The patient is a 39-year-old non-smoking male/female with a history of Meniere's disease and an allergy to Bactrim.
He/she presents with abdominal pain that began abruptly 2 hours ago and has persisted despite taking NEFOPAM 45 minutes ago.
This is his first episode.
His/her vital signs are blood pressure 140/66, heart rate 91, pulse ox 97%, temperature 36.8°C.
He/she rates his/her pain as 8/10 without any analgesic position.
On clinical examination he/she presents with localized epigastric tenderness.
The rest of the abdomen is soft, painless and depressed.
There are hydro-aeriform noises.
No diarrhea or vomiting.
The rest of the clinical examination showed no abnormalities.".
In the intervention case, patient had history of S
|
|
black woman
the case will present a black woman
|
The intervention consisted of a randomized questionnaire presenting a clinical case of a patient suffering from severe abdominal pain.
The control case was "As an emergency physician in an adult emergency department, you are presented with the following patient: The patient is a 39-year-old non-smoking male/female with a history of Meniere's disease and an allergy to Bactrim.
He/she presents with abdominal pain that began abruptly 2 hours ago and has persisted despite taking NEFOPAM 45 minutes ago.
This is his first episode.
His/her vital signs are blood pressure 140/66, heart rate 91, pulse ox 97%, temperature 36.8°C.
He/she rates his/her pain as 8/10 without any analgesic position.
On clinical examination he/she presents with localized epigastric tenderness.
The rest of the abdomen is soft, painless and depressed.
There are hydro-aeriform noises.
No diarrhea or vomiting.
The rest of the clinical examination showed no abnormalities.".
In the intervention case, patient had history of S
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Morphine prescription
Time Frame: through study completion, an average of 1 year
|
The proportion of patient for which physician would have prescribed morphine
|
through study completion, an average of 1 year
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Analgesic prescription between groups
Time Frame: through study completion, an average of 1 year
|
To compare analgesic prescription between groups
|
through study completion, an average of 1 year
|
|
factors associated with differences in management between groups
Time Frame: through study completion, an average of 1 year
|
identify factors associated with differences in management (urgency level, morphine prescription and computed tomography scan ordering)
|
through study completion, an average of 1 year
|
|
Differences according to patient and practitioner gender
Time Frame: through study completion, an average of 1 year
|
analyze the difference in morphine treatment prescribed according to patient and practitioner gender
|
through study completion, an average of 1 year
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
February 17, 2025
Primary Completion (Actual)
March 19, 2025
Study Completion (Actual)
March 19, 2025
Study Registration Dates
First Submitted
February 10, 2025
First Submitted That Met QC Criteria
February 14, 2025
First Posted (Actual)
February 19, 2025
Study Record Updates
Last Update Posted (Actual)
January 23, 2026
Last Update Submitted That Met QC Criteria
January 21, 2026
Last Verified
January 1, 2026
More Information
Terms related to this study
Additional Relevant MeSH Terms
- Neurologic Manifestations
- Nervous System Diseases
- Genetic Diseases, Inborn
- Neurobehavioral Manifestations
- Hematologic Diseases
- Anemia, Hemolytic, Congenital
- Anemia, Hemolytic
- Anemia
- Hemoglobinopathies
- Perceptual Disorders
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities
- Pathological Conditions, Signs and Symptoms
- Behavior
- Signs and Symptoms
- Hemic and Lymphatic Diseases
- Social Behavior
- Prejudice
- Social Discrimination
- Anemia, Sickle Cell
- Agnosia
- Racism
- Physiological Effects of Drugs
- Peripheral Nervous System Agents
- Central Nervous System Depressants
- Sensory System Agents
- Analgesics
- Narcotics
- Analgesics, Opioid
Other Study ID Numbers
- 25.02.01
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
product manufactured in and exported from the U.S.
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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