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Optimal HCTZ Cessation for Diagnosis of Hyperparathyroidism

University of Missouri (MU) logo

University of Missouri (MU)

Status

Completed

Conditions

Hyperparathyroidism

Treatments

Procedure: HCTZ cessation

Study type

Interventional

Funder types

Other

Identifiers

NCT02591160
1213821

Details and patient eligibility

About

Primary hyperparathyroidism (PHPT) is the most common cause of hypercalcemia in the ambulatory setting. PHPT may be cured with surgery and indications for intervention have been defined and include urinary calcium/creatinine clearance. Hydrochlorothiazide (HCTZ), the most commonly prescribed medication for hypertension, reduces urinary calcium excretion and confounds urinary testing. As a result, it is universally recommended that thiazide diuretics be stopped in advance of urinary testing. To date, no studies are available to provide evidence-based guidance as to how long HCTZ must be held for urinary calcium excretion to return to steady state in PHPT. The objective of this study is to serially calculate urinary calcium/creatinine clearance ration in patients with suspected PHPT while holding HCTZ to determine the minimum duration of medication cessation necessary for urinary calcium clearance to reach steady state.

Full description

In this study, adult patients will submit serum and 24 hour urine samples prior to HCTZ cessation and at the following intervals after cessation: 4-6 days, 14-16 days, 28-30 days, adn 90-92 days. To minimize confounding variable, patients will take supplemental Vitamin D and Calcium, monitor their daily calcium intake, and monitor blood pressure weekly. Alternative, non-diuretic, antihypertensive medication(s) may be prescribed at the discretion of the enrolling provider.

Enrollment

2 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. Elevated calcium on at least two separate draws with coexistent elevated parathyroid hormone (PTH) on at least one occasion.
  2. Taking Hydrochlorothiazide for hypertension
  3. Following a "wash period", patients must have a normal range 25-hydroxy Vitamin D level, thyroid stimulation hormone (TSH) and serum magnesium levels.
  4. Controlled blood pressure
  5. Willingness to comply with serial sampling
  6. English as the primary language
  7. Adults 18 years and older

Exclusion criteria

  1. Unable to cease Hydrochlorothiazide for any reason
  2. Congestive heart failure
  3. Renal insufficiency (GFR <60)
  4. Cardiovascular event in the last 3 months - include myocardial infarction, new onset atrial fibrillation, and new onset bundle branch block
  5. Take lithium or other diuretic medication in last 3 months
  6. Positive family history of familial hypocalciuric hypercalcemia (FHH)

Trial design

Primary purpose

Diagnostic

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

2 participants in 1 patient group

HCTZ cessation
Other group
Description:
Patients will stop taking HCTZ for 3 months while submitting serial blood and 24 hour urine samples
Treatment:
Procedure: HCTZ cessation

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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