The DENOCHARCOT Trial

Ole Lander Svendsen

Status and phase: Enrolling; Phase 3

Conditions: Charcot Foot; Diabetes Mellitus

Treatments: Drug: Denosumab Injection

Study type: Interventional

Funder types: Other

Identifiers

NCT04547348

CODIF-008

Details and patient eligibility

About

The aim of the present trial is to assess the efficacy of treatment of acute Charcot foot in diabetes patients with Prolia® on clinical relevant Outcomes in a randomized, double blind, placebo-controlled trial.

Full description

After giving informed consent and being enrolled, patients will be randomized to one of two group given either Denosumab treatment or injection with placebo. The patients will then undergo a 52 week follow up with regular controls to asses if clinical signs of Charcot is in remission, which will be verified using relevant radiological modalities. Upon final visit the patients will be examined using radiology, blood samples, biothesiometry and objective examinations, following up on the same examinations being made upon inclusion.

Primary outcome will be time until full remission of the Charcot foot defined as clinical healing (The acute Charcot foot is clinically healed when the temperature difference at the site maximum temperature on the affected Charcot foot is < 2 degrees Celsius compared to the similar site on the contra-lateral foot, measured using an infrared thermometer, and edema and redness of the skin has subsided) followed up by radiological signs of healing.

Enrollment: 38 estimated patients

Sex: All

Ages: 18 to 80 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Age 18-80 years
• Type 1 or type 2 diabetes (diagnosed diabetes for more than 3 months)
• Diagnosed with acute Charcot foot defined as a unilateral red, swollen and warm foot, with a difference of skin temperature of more than 2 °C compared with the unaffected foot and with sign of Charcot on either x-rays of the foot, MRI, bone scintigram or PET/CT.
• Peripheral neuropathy: Previously diagnosed and/or biothesiometri: > 25 V or lack of sensation of 10 grams monofilament on 1. toe at the acute Charcot foot.

Exclusion criteria

• Duration of the acute Charcot foot for more than 3 months (at the screening visit).
• Existing foot ulcer on the affected foot
• Previous acute or chronic Charcot of the affected foot
• Planned surgery on the acute Charcot foot
• Infection (cellulitis or osteomyelitis) of the affected foot (clinically and/or radiologically proven)
• Previous midfoot or proximal to mid foot amputation of the affected foot
• Hypocalcemia (Serum Calcium <2.1 mmol/L or Calcium ion < 1.12 mmol/L)
• Vitamin D deficiency (Serum 25-hydroxyvitamin D < 50 nmol/L)
• Renal failure (serum creatinine >200 mmol/L or eGFR < 30 ml/min).
• Treatment with Denosumab within the last 12 months. • Have a known hypersensitivity to Denosumab • History of osteonecrosis of the jaw.
• Poor oral hygiene, which is defined as within 3 months of a tooth extraction, dental implants or mandibular surgery
• Planned mandibular surgery or dental implants within the next 12 months.
• Prior non-traumatic vertebral fracture
• Treatment with medication known to affect bones within the last 12 months (such as bisphosphonates, Forsteo®, calcitonin, Protelos®, selective estrogen receptor modulators, glucocorticoids and sex hormones)
• Active or chronic liver disease *Chronic liver disease is defined as clinical history of decompensated chronic liver disease (ascites, encephalopathy or variceal bleeding) *Acute Liver disease is defined as an INR of > 1.5 (in the absence of the use of Warfarin) and AST and ALT > 2 x ULN
• History of inflammatory arthropathies (rheumatoid arthritis, ankylosing spondylitis, psoriatic arthritis, autoimmune arthropathy)
• Pre-existing medical condition judged to preclude safe participation in the study
• Current treatment with cytotoxic drugs or with systemically administered glucocorticoids
• Abuse of alcohol or drugs, or presence of any condition that in the Investigators opinion may lead to poor adherence to study protocol
• Pregnancy, breast feeding or planning pregnancy or not using adequate contraceptive methods. The following contraceptive products are considered to be safe: Intrauterine devices or hormonal contraception (oral contraceptive pills, implants, transdermal patches, vaginal rings or long-acting injections).
• Likely inability to comply with the visits because of planned activity
• Use of any investigational product with the last month.
• Use of any drug or any other reason which in the Investigator's opinion could interfere with the outcome of the treatment of the acute Charcot foot.
• Cancer, or any clinically significant disease or disorder, except for conditions associated to the diabetes, which in the Investigator's opinion could interfere with the results of the trial

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Triple Blind

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38 participants in 2 patient groups, including a placebo group

Denosumab treated group

Experimental group

Description:

Participants will receive a 60 mg subcutaneous injection of Prolia upon randomization and on week 28 after the first injection provided remission of the Charcot foot has not been achieved by then

Treatment:

Drug: Denosumab Injection

Placebo treated group

Placebo Comparator group

Description:

Participants will receive an injection of placebo (saline) instead of Prolia

Treatment:

Drug: Denosumab Injection