Safety and Efficacy of a Lipiodol Emulsion for the Embolization of Hypervascularizations in Patients With Knee Pain (LipioJoint1)

Knee Osteoarthritis Clinical Trial

— LipioJoint1  

Official title:

Prospective Study of the Safety and Efficacy of the Use of a Lipiodol Emulsion for the Embolization of Inflammatory Hypervascularizations Observed in Patients With Joint or Abarticular Knee Pain

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT04733092
• Other study ID #: APHP190891
• Secondary ID: 2020-002206-10
• Status: Completed
• Phase: Phase 1
• Start date: March 3, 2021
• Est. completion date: September 20, 2022

Study information

• Verified date: August 2023
• Source: Assistance Publique - Hôpitaux de Paris
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Knee osteoarthritis is a common cause of disability in patients who are often young and active. Surgery being an option only for the most severe cases, there is little alternative in case of failure of recommended medication. Inflammatory hypervascularization of the joint is a known source of pain. Temporary embolization of intra-arterial inflammatory hypervascularization has been used since 2012 with good results on pain relief to treat patients with musculoskeletal disorders that are resistant to conventional treatments. Lipiodol® has transient embolizing properties when in emulsion with a contrast agent. It has been used as an emulsion with chemotherapy for the treatment of metastases and primary intra-arterial liver cancer (chemo-embolization) for many years without serious side effects. We hypothesized that Lipiodol® in emulsion could serve as a temporary embolization agent for the treatment of inflammatory hypervascularization responsible for musculoskeletal disorders in humans.

Description:

It is a Phase 1, Single-Arm, Open-label, Multicenter Interventional Prospective Study. In order to ensure the best possible patient safety, a sequential inclusion of the first 6 patients is planned. Thus, the inclusion of each subsequent patient (patient 2-6) will only be considered after reviewing previously included patient safety data. Safety data after the inclusion of each patient (after a step-back of at least one week), as well as the cumulative review of previously included patient safety data, will be brought to the attention of all investigators involved in this research. In addition, the following information will be transmitted to the Competent Authority without delay: - a review of the safety and efficacy of the first 3 patients included with a step back for the last patient of at least one week after the administration of the experimental drug, as well as an argument as to the continuation of this research with regard to these data, with a discussion of the risks incurred in relation to the expected profit - a review of the safety and effectiveness of the first 3 patients after the inclusion of the first 6 patients, as well as an argument as to the continuation of this research with regard to these data, with a discussion of the risks incurred compared to the expected benefit. The patients will be embolized by the Interventional Radiology Department of the European Hospital Georges Pompidou (HEGP). Embolization will be performed by an experienced radiologist during a conventional hospitalization or a day hospitalization. A clinical follow-up will be carried out at 1 week, 1 month and 3 months after embolization by clinics and patient self-assessment (WOMAC, SF-36).

Recruitment information / eligibility

• Status: Completed
• Enrollment: 22
• Est. completion date: September 20, 2022
• Est. primary completion date: June 20, 2022
• Accepts healthy volunteers: No
• Gender: All
• Age group: 35 Years to 90 Years

Eligibility

Inclusion Criteria:

• Diagnosis of primary inflammatory knee osteoarthritis of the target joint defined by a knee osteoarthritis according to the American College of Rheumatology (ACR) classification and a score = 2 according to the classification of Kellgren and Lawrence
• Patient not eligible for surgery (or refusing surgery)
• Analog Visual Scale (VAS) pain = 40 mm despite analgesic treatment for at least 3 months
• Failure or intolerance of treatment with NSAIDs and/or tramadol and/or acetaminophen, and/or failure or intolerance or patient refusing strong opioids medication (morphine, codeine)
• Failure or patient refusal of corticosteroid infiltration
• Patient who has signed an informed consent

Exclusion Criteria:

• Patient who is unable or unable to comply with the follow-up schedule
• Infiltration of target joint less than three months old
• Treated hyperthyroidism
• Traumatic injury, hemorrhage or bleeding less than 1 week old in the target joint
• Known arterial disease of the lower limbs stage = 2 according to the classification of Leriche and Fontaine
• Known severe allergy to Lipiodol® and/or iodized contrast product
• Known severe kidney failure (creatinine clearance < 30 ml/min)
• Pregnant or breastfeeding woman
• Patient not affiliated with a French Medicare
• Patient benefiting from legal protection
• Participation in another interventional research

Related Conditions & MeSH terms

• Knee Osteoarthritis
• Osteoarthritis
• Osteoarthritis, Knee

Intervention

Drug:
• Lipiodol
Lipiodol in emulsion with contrast agent

Locations

Country	Name	City	State
France	Hôpital européen Georges Pompidou	Paris

Sponsors (2)

Lead Sponsor	Collaborator
Assistance Publique - Hôpitaux de Paris	Guerbet

Country where clinical trial is conducted

France, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Serious Adverse Events (SAE)	Number of SAE related to Embolization	1 month
Secondary	Immediate Technical success	Success of catheterization and embolization of target hypervascularization	Intraoperative
Secondary	Pain improvement 1 week after embolization	Analog Visual Scale score (0-100) comparison to baseline VAS score is determined by measuring in millimetres from the left hand end of the line to the point that the patients marks. The Scale is rated from 0 to 100 (no pain to extremely severe pain)	1 week
Secondary	Pain improvement 1 month after embolization	Analog Visual Scale score (0-100) comparison to baseline VAS score is determined by measuring in millimetres from the left hand end of the line to the point that the patients marks. The Scale is rated from 0 to 100 (no pain to extremely severe pain)	1 month
Secondary	Pain improvement 3 month after embolization	Analog Visual Scale score (0-100) comparison to baseline VAS score is determined by measuring in millimetres from the left hand end of the line to the point that the patients marks. The Scale is rated from 0 to 100 (no pain to extremely severe pain)	3 months
Secondary	Articular impotence improvement 1 week after embolization	Western Ontario and McMaster Universities Osteoarthritis Index score (0-96) comparison to baseline	1 week
Secondary	Articular impotence improvement 1 month after embolization	Western Ontario and McMaster Universities Osteoarthritis Index score (0-96) comparison to baseline	1 month
Secondary	Articular impotence improvement 3 month after embolization	Western Ontario and McMaster Universities Osteoarthritis Index score (0-96) comparison to baseline	3 months
Secondary	Quality of life improvement 3 month after embolization	Short Form Health Survey (SF-36) score comparison to baseline SF-36 consists of eight scaled scores which are the weighted sums of the questions in their section, a score of zero is equivalent to maximum disability and a score of 100 is equivalent to no disability.	3 months
Secondary	Pain medication improvement 1 week after embolization	Dose of analgesic medication compared to baseline (mg/24h)	1 week
Secondary	Pain medication improvement 1 month after embolization	Dose of analgesic medication compared to baseline (mg/24h)	1 month
Secondary	Pain medication improvement 3 month after embolization	Dose of analgesic medication compared to baseline (mg/24h)	3 months
Secondary	Patient's satisfaction	Patient's satisfaction questionnaire : qualitative questionnaire with 5 ordered modalities (0 = no to 4 = yes)	3 months
Secondary	Adverse Events (AE)	Number of AE related to embolization	3 months
Secondary	Serious Adverse Events (SAE)	Number of SAE related to embolization	3 months