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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05848531
Other study ID # B0762023230104
Secondary ID
Status Recruiting
Phase Phase 4
First received
Last updated
Start date April 25, 2023
Est. completion date February 28, 2024

Study information

Verified date April 2023
Source Centre Hospitalier Universitaire Saint Pierre
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Vaso-occlusive crisis are highly painful in Sickle-cell patients. Morphine is the treatment of choice for this pain. Various adjuncts have been studied for the treatment of vaso-occlusive crisis. The investigators aimed to study the effect of clonidine associated with morphine in PCIA (patient controlled intravenous analgesia pumps) regimen. The investigators will compare it to the morphine alone in PCIA for the treatment of vaso-occlusive pain. The investigators will measure the morphine consumption of all patient, the impact on the apparition of the morphine secondary effect and on inflammation biomarkers and the biopsychosocial respond. Each patient will be hospitalized and follow by haematologist from the hospital, pain doctors and nurses. It will be a double blind randomised, prospective study. The randomisation will be done by the pharmacy.


Recruitment information / eligibility

Status Recruiting
Enrollment 40
Est. completion date February 28, 2024
Est. primary completion date December 31, 2023
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Vaso-Occlusive Crisis In Sickle Cell disease Patients Exclusion Criteria: - Minor - Patient's refusal - Pregnancy - Contr-indication Clonidine therapy

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Clonidine
Comparing Clonidine with Morphine PCIA for the treatment of Vaso-Occlusive crisis in Sickle Cell disease patient

Locations

Country Name City State
Belgium CHU Saint-Pierre Bruxelles

Sponsors (1)

Lead Sponsor Collaborator
Centre Hospitalier Universitaire Saint Pierre

Country where clinical trial is conducted

Belgium, 

References & Publications (1)

Kenney MO, Smith WR. Moving Toward a Multimodal Analgesic Regimen for Acute Sickle Cell Pain with Non-Opioid Analgesic Adjuncts: A Narrative Review. J Pain Res. 2022 Mar 31;15:879-894. doi: 10.2147/JPR.S343069. eCollection 2022. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Morphine Consumption Morphine Consumption during hospitalisation Up to two weeks
Secondary Numerical Rating Scale Pain Score scale from 0 to ten during and after treatment Up to two weeks
Secondary Biology markers Inflammatory biology markers (CRP,IL-6) and Hemolysis (LDH) Up to two weeks
Secondary Biopsychosocial model / ASCQ-ME questionary Evaluation of the biopsychosocial model. There are seven different themes of 4 to 7 questions each (pain intensity, pain episodes, sleep impact, social impact, emotional impact, medical history and stiffness) Up to two weeks
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