AzTrials
AzTrials

HypercalcemiaNCT04292288

Hypercalcemia After Paraffin Oil Injection

An observational study of Hypercalcemia and Granuloma, run by Martin Blomberg Jensen at 1 site in Denmark.

Recruiting

Looking for participants now. Contact the study team or a site below to ask about taking part.

Sites and contacts
Official record
Search all trials

Trial summary

Today, there is an increased use of non-medical, invasive cosmetic treatments globally without sufficient awareness of possible health risks. A particular problem is young men injecting large amounts of paraffin oil into skeletal muscles especially on upper arms and chest to increase the visible size of the muscles. Read more about this study

Who is it for?
Ages 18 to 80 years, men only
Conditions the study is for
Hypercalcemia, Granuloma
What is being tested?
Biochemical observational
How many people
200 participants
Where
1 siteDenmark
Study dates
1 Apr 2019to 1 Jan 2029
Phase
Observational
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 80 years
  • Men only
  • No healthy volunteers
  • Adult, Older adult

Study population: Up to 200 people (predominantly men) <80 years will be included. Inclusion takes place at Endocrinological Section, Medical Department O, Herlev Hospital in connection with an outpatient visit. After initial discussions, reflection time and acceptance of participation in the study, extended blood tests are taken in connection with the pre-planned outpatient visits.

Who may be able to join

None listed.

Who cannot join

  • inability to understand the consequences of inclusion
  • incurable cancer disease

Trial locations and contacts

1 site in 1 country. Contact the study team or a site near you to ask about taking part.

Martin Blomberg Jensen contact

+4535453545

blombergjensen@gmail.com

Denmark1 site, 1 recruiting
  • Herlev Hospital

    Herlev

    Ebbe Eldrup, +4538683868

    Martin Blomberg Jensen

    Recruiting

Other trials in Denmark

About this study

Official title: Hypercalcemia After Paraffin Oil Injection: Aetiology, Pathogenesis and Possible Treatment Options

Today, there is an increased use of non-medical, invasive cosmetic treatments globally without sufficient awareness of possible health risks. A particular problem is young men injecting large amounts of paraffin oil into skeletal muscles especially on upper arms and chest to increase the visible size of the muscles. Several case reports have suggested that intramuscular injection of paraffin oil induces foreign body reaction and granuloma formation and subsequently hypercalcemia. Our hypothesis is that increased generation of activated vitamin D (1,25(OH)2D3) in the marcrophages may be responsible for the persistent hypercalcemia. Now trhe investigators want to include a large group of men who injected 100-10.000 ml paraffin oil to identify risk factors for developing hypercalcemia and try to understand the pathogenesis of the disease. Additionally, granuloma tissue from selected patients will be cultured ex vivo to investigate whether they produce 1,25(OH)2D3 or PTHrP and to test which drugs can most effectively be used to lower calcium levels in these men. Subsequently, we will try to stratify the men according to the severity of the changes in calcium homeostasis as we suggest that this stratification will be the basis for future intervention trials

Read the detailed description

Today, there is an increased use of non-medical, invasive cosmetic treatments globally without sufficient awareness of possible health risks. A particular problem is young men injecting large amounts of paraffin oil into skeletal muscles especially on upper arms and chest to increase the visible size of the muscles. Several case reports have suggested that intramuscular injection of paraffin oil induces foreign body reaction and granuloma formation. The formation of granuloma probably precedes the marked hypercalcemia that often develops and appears to be difficult to treat. The largest study to date included 14 men and showed that practically all men developed serious hypercalcemia, but the etiology was unclear. Foreign body granulomas are like other granulomatous diseases such as Tuberculosis or sarcoidosis rich in macrophages, (ref) and it has been proposed that increased generation of activated vitamin D (1,25(OH)2D3) in the marcrophages may be responsible for the persistent hypercalcemia.

Calcium homeostasis is tightly regulated primarily by vitamin D, Parathyroid hormone (PTH) and Fibroblast growth factor 23 (FGF23) that rapidly modifies intestinal absorption, renal excretion and calcium mobilization from the skeletal compartment in response to immediate changes in serum calcium (ref). Vitamin D (cholecalciferol) is normally formed by UV-B radiation of the skin and requires two enzymatic reactions before it can bind and activate the vitamin D receptor (VDR). Conversion of cholecalciferol to 25-hydroxydvitamin (25OHD) is the first activation step; it is un-regulated and generally exerted by the hepatic CYP2R1. 25OHD is not biologically active and must undergo 1-alpha hydroxylation by renal CYP27B1 to form the active metabolite 1,25(OH)2D3. The main actions of 1,25(OH)2D3 is to promote calcium and phosphate absorption and decrease calcium excretion until inactivated by CYP24A1. 1,25(OH)2D3 is also a powerful inhibitor of PTH and inducer of FGF23, which ensures an important feedback-loop to maintain an adequate vitamin D status (ref). PTH which is a potent inducer of CYP27B1, mobilizes calcium and phosphate from the skeleton and increases phosphate excretion. In contrast, FGF23 that inhibits CYP27B1, induces the in-activating CYP24A1 and promotes phosphate excretion. Almost all organs has the ability to activate, respond to, and inactivate vitamin D because CYP27B1, VDR and CYP24A1 are expressed also in most non-renal tissues. However, regulation of CYP27B1 and CYP24A1 is strikingly different in these organs where high intracellular levels of 1,25(OH)2D3 activates VDR that induces transcription of CYP24A1 and thereby increases in-activation to restore normal intracellular levels of all vitamin D metabolites. This autoregulatory control of vitamin D metabolites secures under normal circumstances that high concentrations of 1,25(OH)2D3 are not released into circulation. Regulation of vitamin D homeostasis is different in the macrophages present in granulomas because they retain a splice variant of CYP24A1 that is not upregulated in response to high 1,25(OH)2D3 levels, which in part explains the increased release of 1,25(OH)2D3 in granulomatosis disease. Another important issue is aberrant regulation of CYP27B1 in macrophages, which is induced by inflammatory signals such as interleukin-2 and TNF-alpha rather than PTH. Previous case reports have detected CYP27B1 expression in granuloma tissue by immunohistochemistry. However, these findings have to our knowledge never been corroborated by a more comprehensive analysis of enzyme activity and a recent study questioned the etiology because most men with granulomas had normal levels of 1,25(OH)2D3 in serum (ref).

In the present study the investigators want to include a large group of men who injected 100-10.000 ml paraffin oil to identify risk factors for developing hypercalcemia and try to understand the pathogenesis of the disease. Additionally, granuloma tissue from selected patients will be cultured ex vivo to investigate whether they produce 1,25(OH)2D3 or PTHrP and to test which drugs can most effectively be used to lower calcium levels in these men. Subsequently, elucidate whether it is possible to stratify the men according to the severity of the changes in calcium homeostasis as such a stratification may be required prior to and form the basis for future intervention trials

Being tested
Biochemical observational
Medical subject headings
Hypercalcemia, Granuloma

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Biochemical observationalDiagnostic test

    no intervention - observational

Study groups in NCT04292288
Study groupRoleWhat they receive
Foreign body granulomamen injecting paraffin oil
Receives: Diagnostic Test: Biochemical observational

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Hypercalcemia

    the number of men with elevated ionized calcium (above 1.32 mmol/l)

    Measured: determined 2-10 years after paraffin oil injection (first visit)

  2. production of 1,25OHD3

    production of 1,25OHD3 determined in media from granuloma tissue culture compared with kidney culture by ELISA platform

    Measured: ex vivo culture experiments of human granuloma tissue for 48 to 72 hours

Secondary outcomes (11)
  1. hypercalciuria

    calcium excretion determined by spot or 24 hour urine

    Measured: determined 2-10 years after paraffin oil injection

  2. change in serum 1,25OH2D3

    differences in calcitriol production or conversion rate 1,25OH2D3/25OHD that reflects how active the enzyme is

    Measured: determined 2-10 years after paraffin oil injection (first visit)

  3. nephrolithiasis

    obtained by interview -anamnesis and preferably supported by jorunal of CT report on nephrolithiasis

    Measured: determined 2-10 years after paraffin oil injection (first visit)

  4. Overall change in calcium homeostasis

    changes in calcium, PTH, alkaline phosphatase and 1,25OHD depending on oil injected, varm/cold

    Measured: determined 2-10 years after paraffin oil injection (first visit)

  5. inflammatory response

    changes in inflammatory markers IL2R, ferritin, ACE

    Measured: determined 2-10 years after paraffin oil injection (first visit)

  6. Bone formation and resorption

    Serum levels of alkaline phosphatase, C-terminal telopeptide of type I collagen (CTX-I) and N-terminal propeptide of type I procollagen (PINP)

    Measured: determined 2-10 years after paraffin oil injection (first visit)

  7. renal function

    change in GFR, creatinine, Urea

    Measured: determined 2-10 years after paraffin oil injection (first visit)

  8. calciphylaxis

    risk determined by Calcium - phosphate product

    Measured: determined 2-10 years after paraffin oil injection (first visit)

  9. Suppressed PTH

    PTH lower than lower reference (2)

    Measured: determined 2-10 years after paraffin oil injection (first visit)

  10. suppression of 1,25OHD3 production

    production of 1,25OHD3 released into the media from granuloma culture suppressed by different treatments in vitro

    Measured: ex vivo culture experiments of human granuloma tissue exposed to treatments for 48 and 72 hours

  11. production of PTHrP

    PTHrP production in granuloma determined by ELISA platform

    Measured: ex vivo culture experiments of human granuloma tissue for 48 and 72 hours

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted3 Mar 2020
  2. Study start1 Apr 2019
  3. Primary completion1 Jan 2028 (estimated)
  4. Study completion1 Jan 2029 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Cohort
Time perspective
Prospective
Enrolment
200 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT04292288
Sponsor's protocol ID
H-19010297
Status last verified
Apr 2025
First submitted
26 Sep 2019
Last updated
6 Apr 2025
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Questions about this trial

What is this clinical trial studying?

An observational study of Hypercalcemia and Granuloma, run by Martin Blomberg Jensen at 1 site in Denmark.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 0 inclusion and 2 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: looking for participants now, as of the sponsor's last update on 6 Apr 2025. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Denmark. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

Contact Martin Blomberg Jensen (+4535453545, blombergjensen@gmail.com), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Hypercalcemia (time frame: determined 2-10 years after paraffin oil injection (first visit)). The study lists 2 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 6 Apr 2025.

Free account

Keep searching with a free account

You’ve used your 3 free searches for this session. Log in or create a free AzTrials account to keep searching clinical trials and save the ones you want to follow.

Create a free accountLog in