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The GranStone Trial

2026年9月17日 更新者:Martin Blomberg Jensen

Prevention of Kidney Stones Due to Paraffin Oil Induced Granuloma: A Prospective Interventional Study

This study will investigate whether treatment with empagliflozin or losartan can reduce the risk of kidney stone formation in patients with paraffin disease, a condition caused by the injection of paraffin oil into muscle tissue for cosmetic muscle enlargement.

Paraffin disease can lead to chronic inflammation, disturbances in calcium regulation, high blood calcium levels, kidney stones, and impaired kidney function. Previous studies from Herlev-Gentofte Hospital have shown that kidney stones occur in nearly half of affected patients, while approximately one-third develop reduced kidney function. Current treatment primarily consists of high-dose corticosteroids, which can reduce blood calcium levels but cause substantial adverse effects and may not adequately control the underlying disease process.

Both empagliflozin and losartan are widely used medications with documented kidney-protective effects in other chronic kidney diseases. This randomized clinical trial will evaluate whether either treatment can prevent kidney stone formation and slow kidney-related complications in patients with paraffin disease.

The purpose of this study is to determine whether treatment with empagliflozin or losartan can prevent kidney stone formation and improve kidney health in patients with paraffin disease.

研究概览

详细说明

Cosmetic treatments are becoming increasingly popular, now also encompassing injection of different sorts of fillers. One such approach is the injection of paraffin oil into muscular regions for the sole purpose of enhancing muscular size. During the last 4 years we have experienced that injections with paraffin oil are being more widely used than anticipated. Usage is mainly seen in the younger segment of the male Danish population, causing severe morbidity including hypercalcemia, kidney stones and renal failure in patients often in their thirties. Injected paraffin oil causes foreign body reactions, leading to inflammation and granuloma formation. Granulomas are rich in macrophages capable of producing large amount of activated vitamin D (1,25OH2D3) that may cause severe hypercalcemia. Although, the link between foreign body granuloma, and hypercalcemia has been known for more than 60 years sparse evidence-based treatments exist to control calcium and vitamin D balance in these patients. Physiologically, cutaneous produced or orally absorbed 25OH2D3 (cholecalciferol) needs activation before it can activate the vitamin D receptor (VDR) and exert its actions. This activation occurs through hydroxylation by CYP27B1 in the kidneys creating the active 1,25(OH)2D3 (calcitriol). CYP27B1 is the rate-limiting step in calcitriol synthesis and is tightly regulated under physiologic conditions. Control of high 1,25(OH)2D3 is achieved by a feedback system, where 1,25(OH)2D3 stimulates the enzyme CYP24A1, which in turn hy-droxylate 1,25(OH)2D3 to the inactive 1,24,25OH2D3. Several other players, e.g. parathy-roid hormone (PTH) and fibroblast growth factor 23 (FGF23) regulate calcium homeostasis. However, in macrophages, CYP27B1 is upregulated by interleukin 2, and the inhibiting enzyme CYP24A1 is not upregulated. Therefore, granulomas can produce large amounts of 1,25OH2D3, and this production is not counteracted by the otherwise tight regulatory and physiological mechanisms. Unimpeded 1,25OH2D3 in turn increase calcium absorption from the intestines, reabsorption from the kidneys and to some extent calcium release from bones, all leading to hypercalcemia. Hypercalcemia is a late feature of accelerated 25OH2D3 activation, as several counter regulatory mechanisms will attempt to maintain normocalcemia. As a result, these patients suffer from nephrolithiasis or progressive kidney disease due to nephrocalcinosis and/or nephrolithiasis, with some patients progressing to end stage renal dis-ease (ESRD).

SGLT2 inhibitors were developed for treatment of type 2 diabetes to lower blood glucose levels but they had a more pronounced effect in patients with heart or renal failure irrespective of diabetes status. SGLT2 inhibitors could prevent or reduce eGFR decline in patients with renal failure and it appeared in some trials that it could also lower the risk of nephrolithiasis. SGLT2 inhibitors have few adverse effects in non-diabetics and may be used to prevent progression of paraffin oil disease by protecting the kidney and reducing the risk of kidney stones in these patients. ACEi's and ARB's have also been shown to reduce progression of kidney disease. Although the data on prevention of kidney stones is less convincing for ACEi/ARB's the renoprotective effects make them a potential treatment option.

Data from our cohort of patients:

During our initial investigation of 88 patients, milder symptoms of hypercalcemia were often accompanied by hypercalcuria with increased risk of kidney stones and later nephrocalcinosis and ultimately progressive renal failure and vascular calcification as seen in patients with primary hyperparathyroidism or CKD. 3 deaths have been recorded in our cohort of young men, so paraffin disease leads to significant morbidity, but presumably also increased mortality. Currently, paraffin disease is still very sparsely described in the medical literature. The number of affected individuals is presumably large because early disease causes few symptoms and many of these men rarely seek medical attention. At the section of Endocrinology at Herlev-Gentofte Hospital, there is currently more than 310 young males who injected paraffin oil prior to referral. In the first published cohort of 88 males (32 ± 7 years (mean ± SD)) who injected paraffin oil 6 years prior to their first visit, the minority (42%) have managed to maintain an apparent normal calcium metabolism (normocalcemic and normoparathyoid), while the majority have developed an abnormal calcium metabolism ranging from normocalcemic and hypoparathyroid (24%) to hypercalcemic and hypoparathyroid (34%). Renal stone formers ranging from 22 % in patients with an apparent normal calcium homeostasis to a stunning 47-48% in those with abnormal calcium homeostasis (5-10% in back-ground population). Importantly, a significant number of patients (approx. 30%) had already developed mild to severe renal impairment with reduced eGFR. Most patients tended to have increased inflammatory markers (interleukine-2 receptor (IL-2R) and/or pepti-dyldipeptidase (ACE)) - even in those with apparent normal calcium metabolism. Surgical resection may improve both local reactions and pain. However, due to granuloma formation within muscle tissue and oilmigration, it is difficult to remove all the granuloma tissue. Currently, first line of treatment for paraffin disease is prednisolone, which has proven effective in lowering calcium levels in all our patients. However, patients require relatively large (15-75 mg daily) and long term (years) doses of prednisolone to achieve and maintain normal or near normal calcium levels with many possible adverse effects. Noteworthy, after 4 years observation we have not yet seen any decrease in inflammatory markers in any male suggesting that prednisolone monotherapy is not enough when you have large amount of granuloma tissue. Paraffin disease mimics sarcoidosis, both being granulomatous diseases with hypercalcemia due to macrophage mediated 25OH2D3 activation. Interestingly, RAAS activation has been shown to contribute to sarcoidosis granuloma formation in an ex vivo model, highlighting an additional potential role for treatment with ACEi/ARB's. However, paraffin disease appears to be much more progressive, not self-limiting and require more aggressive treatment probably because the volume of granulomatous tissue is so huge.

Since ACEi's, ARB's and SGLTi's are the only drug classes consistently shown to slow progression in CKD in a non-diabetic population, we hypothesize that these treatments will be effective in a cohort of patients with hypercalcemia due to paraffin oil induced granulomatous disease. Furthermore, we hypothesize that SGLTi will have a greater effect due to the potential decrease in incident nephrolithiasis. However, the ketosis associated with this treatment may not be beneficial, which clearly justifies the face-to-face comparison.

Losartan was chosen over an ACE inhibitor due to ease of administration and proven safety in patients with severe kidney disease. Additionally, it has been suggested that ARB's have greater efficacy than ACEi's on survival in patients with granulomatous disease due to sarcoidosis.

This research project will investigate whether it is of value to initiate nephroprotective treatment with an SGLT2 inhibitor or ARB in patients with hypercalciuria due to paraffin oil induced granulomatous disease.

研究类型

介入性

注册 (估计的)

100

阶段

  • 阶段2
  • 第三阶段

联系人和位置

本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。

学习联系方式

研究联系人备份

学习地点

      • Herlev、丹麦、2730
        • Division of Translational Endocrinology, Department of Endocrinology and Internal Medicine, Copenhagen University Hospital Herlev, Herlev
        • 首席研究员:
          • Martin B Jensen, Professor
        • 副研究员:
          • Emil B Wriedt, MD
        • 接触:

参与标准

研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。

资格标准

适合学习的年龄

  • 成人
  • 年长者

接受健康志愿者

不

描述

Inclusion Criteria:

  • Signed informed consent by participant
  • Male
  • 18-70 years
  • Paraffin granuloma disease with hypercalcemia, hypoparathyroidism, hypercalciuria or a history of nephrolithiasis

Exclusion Criteria:

  • eGFR < 30 ml/min
  • Cancer (past or present, except basal cell skin cancer or squamous cell skin cancer), which in the investigator's opinion could interfere with the results of the trial
  • Type 1 DM
  • Known chronic kidney disease in whom RAS-blockade and SGLT2-inhibition is indicated.
  • Severely impaired liver function
  • History of organ transplantation
  • Receiving therapy with an SGLT2 inhibitor or ATII antagonist within 8 weeks prior to enrollment or previous intolerance of an SGLT2 inhibitor or ATII antagonist.
  • Known history of angioedema
  • Mental incapacity, language barriers or unwillingness to comply with the requirements of the protocol, which may preclude adequate understanding or cooperation during the trial, as judged by the investigator

学习计划

本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。

研究是如何设计的?

设计细节

  • 主要用途:治疗
  • 分配:随机化
  • 介入模型:并行分配
  • 屏蔽:单身的

武器和干预

参与者组/臂
干预/治疗
实验性的:Empagliflozin
Once daily 25 mg tablet PO
Once daily 25 mg tablet PO
有源比较器:Losartan
Once daily 100 mg tablet PO
Once daily 100 mg tablet PO

研究衡量的是什么?

主要结果指标

结果测量
措施说明
大体时间
Image verified new or increased nephrolithiasis or nephrocalcinosis (from 0-24 months).
大体时间:From baseline to end of follow-up at 24 months

The individual components of the composite outcome are defined as follows:

  • If nephrolithiasis- or nephrocalcinosis burden occurs after baseline or aggravates by more than 20% at follow-up it is counted as a positive outcome.
  • Any CT scans conducted as a part of a participant's routine medical care or hospital visits will also be used.
  • In the event that a participant undergoes more than 1 CT scan, it will be counted as a positive outcome if any of the scans shows nephrolithiasis or nephrocalcinosis accord-ing to the criteria above.
  • Symptomatic kidney stone as defined as visible passage of a stone in the urine accom-panied by flank/groin/abdominal pain will also be counted as a positive outcome.
From baseline to end of follow-up at 24 months

次要结果测量

结果测量
措施说明
大体时间
Change in calcium homeostasis after 12 and 24 months
大体时间:From baseline to month 3, 12 and end of follow-up at 24 months
Change in calcium homeostasis after 12 and 24 months defined by either: 1A Change in p-Calcium ion concentration (mmol/L); 1B Change in p-PTH concen-tration (pmol/L); 1C Change in urine calcium excretion (mmol/L).
From baseline to month 3, 12 and end of follow-up at 24 months
Change in estimated glomerular filtration rate (eGFR) (mL/min/1.73 m²)
大体时间:From baseline to month 3, 12 and end of follow-up at 24 months
From baseline to month 3, 12 and end of follow-up at 24 months
Change in p-Creatinine (μmol/L)
大体时间:From baseline to month 3, 12 and end of follow-up at 24 months
From baseline to month 3, 12 and end of follow-up at 24 months
Change in average daily prednisolone dosage (mg) based on cumulative average prednisolone dose.
大体时间:From baseline to month 3, 12 and end of follow-up at 24 months
From baseline to month 3, 12 and end of follow-up at 24 months
Change in inflammatory activity of the granulomas.
大体时间:From baseline to month 3, 12 and end of follow-up at 24 months
Change in inflammatory activity evaluated by changes in p-IL-2R (kU/L) and p-ACE (U/L).
From baseline to month 3, 12 and end of follow-up at 24 months
Change in physical- and mental health scores assessed by the Short-Form 36 questionnaire (SF-36).
大体时间:From baseline to end of follow-up at 24 months
The SF-36 consists of 36 questions designed to assess overall health status. Results are transformed onto a scale from 0 (worst possible health) to 100 (best possible health).
From baseline to end of follow-up at 24 months
Change in serum albumin (g/L)
大体时间:From baseline to month 3, 12 and end of follow-up at 24 months
From baseline to month 3, 12 and end of follow-up at 24 months
Change in urine albumin (mg/L)
大体时间:From baseline to month 3, 12 and end of follow-up at 24 months
From baseline to month 3, 12 and end of follow-up at 24 months
Changes in serum vitamin D metabolites
大体时间:From baseline to month 3, 12 and end of follow-up at 24 months
Changes in serum 25OHD, and 24,25(OH)2D3, and 1,25(OH)2D
From baseline to month 3, 12 and end of follow-up at 24 months
Changes in left ventricular ejection fraction (LVEF) and other indices of cardiac function as measured by transthoracic echocardiography.
大体时间:From baseline to end of follow-up at 24 months
From baseline to end of follow-up at 24 months
Incident or worsening signs of: Systolic- and/or diastolic dysfunction, left ventricular hypertrophy, structural heart disease including valvular pathology
大体时间:From baseline to end of follow-up at 24 months
From baseline to end of follow-up at 24 months
Changes in CT Hounsfield Units in the femoral neck and lumbar vertebrae
大体时间:From baseline to end of follow-up at 24 months
From baseline to end of follow-up at 24 months
Change in Coronary Artery Calcium Score on CT-scan
大体时间:From baseline to end of follow-up at 24 months
Coronary artery calcium (CAC) score measured using the Agatston method on non-contrast cardiac CT; higher scores indicate greater coronary calcified plaque burden.
From baseline to end of follow-up at 24 months
Changes in self-reported kidney stones.
大体时间:From baseline to end of follow-up at 24 months
From baseline to end of follow-up at 24 months
Change in BUN (mmol/L)
大体时间:From baseline to month 3, 12 and end of follow-up at 24 months
From baseline to month 3, 12 and end of follow-up at 24 months
Change in serum phosphate (mmol/L)
大体时间:From baseline to month 3, 12 and end of follow-up at 24 months
From baseline to month 3, 12 and end of follow-up at 24 months
Change in urine phosphate (mmol/L)
大体时间:From baseline to month 3, 12 and end of follow-up at 24 months
From baseline to month 3, 12 and end of follow-up at 24 months
Change in serum magnesium (mmol/L)
大体时间:From baseline to month 3, 12 and end of follow-up at 24 months
From baseline to month 3, 12 and end of follow-up at 24 months
Change in urine magnesium (mmol/L)
大体时间:From baseline to month 3, 12 and end of follow-up at 24 months
From baseline to month 3, 12 and end of follow-up at 24 months
Change in serum iron (µmol/L)
大体时间:From baseline to month 3, 12 and end of follow-up at 24 months
From baseline to month 3, 12 and end of follow-up at 24 months
Change in serum ferritin (µg/L)
大体时间:From baseline to month 3, 12 and end of follow-up at 24 months
From baseline to month 3, 12 and end of follow-up at 24 months
Change in serum FGF23 (ng/L)
大体时间:From baseline to month 3, 12 and end of follow-up at 24 months
From baseline to month 3, 12 and end of follow-up at 24 months
Change in serum Klotho
大体时间:From baseline to month 3, 12 and end of follow-up at 24 months
From baseline to month 3, 12 and end of follow-up at 24 months
Change in urine Ka (mmol/L)
大体时间:From baseline to month 3, 12 and end of follow-up at 24 months
From baseline to month 3, 12 and end of follow-up at 24 months
Change in urine Na (mmol/L)
大体时间:From baseline to month 3, 12 and end of follow-up at 24 months
From baseline to month 3, 12 and end of follow-up at 24 months
Change in urine pH
大体时间:From baseline to month 3, 12 and end of follow-up at 24 months
From baseline to month 3, 12 and end of follow-up at 24 months
Change in urine citrate (mmol/L)
大体时间:From baseline to month 3, 12 and end of follow-up at 24 months
From baseline to month 3, 12 and end of follow-up at 24 months
Change in urine oxalate (μmol/L)
大体时间:From baseline to month 3, 12 and end of follow-up at 24 months
From baseline to month 3, 12 and end of follow-up at 24 months
Change in urine bicarbonate (mmol/L)
大体时间:From baseline to month 3, 12 and end of follow-up at 24 months
From baseline to month 3, 12 and end of follow-up at 24 months
Change in urine uric acid (mmol/L)
大体时间:From baseline to month 3, 12 and end of follow-up at 24 months
From baseline to month 3, 12 and end of follow-up at 24 months

合作者和调查者

在这里您可以找到参与这项研究的人员和组织。

调查人员

  • 首席研究员:Martin B Jensen, Professor、Herlev Hospital

出版物和有用的链接

负责输入研究信息的人员自愿提供这些出版物。这些可能与研究有关。

一般刊物

研究记录日期

这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。

研究主要日期

学习开始 (估计的)

2026年9月1日

初级完成 (估计的)

2029年3月1日

研究完成 (估计的)

2029年4月1日

研究注册日期

首次提交

2026年9月11日

首先提交符合 QC 标准的

2026年9月17日

首次发布 (实际的)

2026年9月18日

研究记录更新

最后更新发布 (实际的)

2026年9月18日

上次提交的符合 QC 标准的更新

2026年9月17日

最后验证

2026年9月1日

更多信息

此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.

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