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Study identifier: NCT06859580 Synced from ClinicalTrials.gov · July 29, 2026
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Bisphosphonate Prior to Parathyroidectomy in Primary Hyperparathyroidism

Condition: Primary Hyperparathyroidism  ·  Sponsor: University of Aarhus

PhasePhase 4
Planned participants140
Who can joinAll sexes, 50 Years to no upper limit
Healthy volunteersNo

About this study

This study is a randomized, double-blinded, placebo-controlled trial investigating the effects of zoledronic acid (ZOL) versus placebo in patients with primary hyperparathyroidism (PHPT) undergoing parathyroidectomy (PTX). PHPT is a common endocrine disorder associated with hypercalcemia, reduced bone mineral density (BMD), increased fracture risk, renal calcifications, and cardiovascular complications. While PTX remains the definitive treatment, the potential role of bisphosphonates in optimizing post-surgical outcomes remains unclear. This trial aims to evaluate whether a single infusion of ZOL prior to PTX impacts bone health, cardiovascular parameters, and renal function one year post-surgery. The primary endpoint is the change in areal bone mineral density (aBMD) at the lumbar spine one year after PTX. Secondary endpoints include changes in aBMD at other skeletal sites, volumetric BMD, bone microarchitecture, bone turnover markers, coronary artery calcium score, arterial stiffness, and renal calcifications. A total of 140 postmenopausal women and men over 50 years with PHPT and low BMD will be enrolled and randomized to receive either ZOL or placebo 2-4 weeks before PTX. Participants will undergo extensive imaging, biochemical analysis, and cardiovascular assessments at baseline and one year post-surgery. This study seeks to clarify whether ZOL improves post-surgical bone recovery or interferes with the natural bone remodeling process following PTX. Additionally, it w…

This description comes directly from the study's public registry record.

Talk to the study team

Anne Louise Vandsø Svenningsen, MD  ·  +45 60183895  ·  ansvnn@rm.dk

Henriette Ejlsmark Svensson, MD, PhD  ·  henrkn@rm.dk

Always discuss trial participation with your own doctor first.

Locations (1)

Aarhus University HospitalAarhus N, Central Region of Denmark, DenmarkRecruiting

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Source record: clinicaltrials.gov/study/NCT06859580