Fact CheckerSign in

NCT07246265Recruiting

Morphine Clearance and Glomerular Filtration in Sickle Cell Patients in Crisis in Intensive Care

Source: ClinicalTrials.gov · Last updated 10 Mar 2026

Brief summary (registry, in English)

Background: Sickle cell disease is a genetic disorder of haemoglobin (which carries oxygen in red blood cells). The shape of sickle cell-patients' red blood cells is abnormal. Thus, red blood cells can be blocked in small vessels, responsible for painful crises due to a lack of downstream circulation. These crisis (acute vaso-occlusive crisis) require strong treatment based on morphine, and often require intensive care.However, treatment is often insufficiently effective. Patient can also experiment acute chest syndrome, a complication of vaso-occlusive crisis, which can be responsible for respiratory failure. In addition, patients with sickle cell disease frequently have kidney damage called sickle cell nephropathy, which in the early stages of the disease is responsible for renal hyperfiltration, meaning that the kidneys filter the blood more than necessary, with faster elimination of drugs. For example, it is known that higher doses of antibiotics must be used in these patients than in the general population for the same effectiveness. The hypothesis of the study is that morphine, a drug eliminated by kidneys, is underdosed in patients with sickle cell disease, which is responsible for the difficulties in achieving sufficient analgesia. Objective: To determine the glomerular filtration rate threshold for which it is necessary to prescribe higher doses of morphine in sickle cell patients with vaso-occlusive crisis. Methods: inclusion of 100 patients admitted to intensive care for an acute vaso-occlusive crisis or acute chest syndrome and receiving morphine. Within 24 hours of study inclusion, four morphine dosages will be performed, in parallel with a precise determination of the glomerular filtration rate by measuring the elimination rate of a tracer, 100% eliminated by the kidneys and injected at the start of the study. This tracer is iohexol, a contrast agent commonly used in radiology. Morphine underdosage will be interpretated regarding glomerular filtration rate. The effectiveness of analgesia and the amount of analgesics required will be also be analyzed. Outlook: At the end of this study, the investigators will be able to offer adapted doses of morphine for sickle cell patients in crisis, adapted to glomerular filtration rate, in the aim of personalizing analgesia.

Status (registry)
Recruiting
Study type
Interventional
Enrollment
100 (estimated)
First submitted
29 Aug 2025
Start date
5 Mar 2026
Primary completion date
30 Sept 2028
Lead sponsor
University Hospital, Tours
NCT number
NCT07246265
EU CT number
2024-511985-34-00

What you commit to

  • Study type: Interventional
  • Planned participants: 100
  • From 5 Mar 2026 to the primary completion date, 30 Sept 2028
  • 6 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Patient previously included in the study during a previous stay
  • Injection of iodinated contrast medium outside the scope of the study within 24 hours prior to inclusion, or scheduled within 9 hours following the scheduled time of iohexol injection
  • Patient undergoing morphine treatment or substitution treatment such as methadone or buprenorphine prior to hospitalization (having received morphine or a derivative regardless of the route of administration in the week prior to hospitalization).

Other illness

  • Contraindication to iohexol: known or suspected immediate or delayed hypersensitivity, thyrotoxicosis.
  • Chronic liver disease likely to interfere with morphine metabolism (cirrhosis )
  • Any condition that contraindicates the use of morphine according to the summary of product characteristics

Other

  • Patients under legal protection
  • Pregnant or breastfeeding women
  • Need for extrarenal epuration within 24 hours of inclusion

Who the study is looking for

  • Patient ≥ 18 years old
  • Known homozygous sickle cell disease SS, SC, S-beta+, or S-beta0
  • Admitted in an intensive care unit
  • Clinical diagnosis of vaso-occlusive crisis and/or acute chest syndrome
  • Receiving PCA treatment with morphine
  • Patient's consent for study participation and/or from a relative if case of patient's incapacity
  • Affiliation to social protection

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (6)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Henri Mondor
Coordinator of this site? Confirm its status
CréteilFranceNot yet recruiting
CH Le Mans
Coordinator of this site? Confirm its status
Le MansFranceNot yet recruiting
CHU de Nantes
Coordinator of this site? Confirm its status
NantesFranceNot yet recruiting
CHU d'Orléans
Coordinator of this site? Confirm its status
OrléansFranceNot yet recruiting
CHU de Rennes
Coordinator of this site? Confirm its status
RennesFranceNot yet recruiting
CHRU de Tours
Coordinator of this site? Confirm its status
ToursFranceRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.