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Changes in Circulating Sclerostin Levels During Acute Postsurgical Hypoparathyroidism

Changes in Circulating Sclerostin Levels During Acute Postsurgical Hypoparathyroidism

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04146259
Enrollment
109
Registered
2019-10-31
Start date
2017-01-01
Completion date
2019-08-01
Last updated
2019-11-01

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Hypoparathyroidism Postprocedural

Keywords

Sclerostin, Hypoparathyroidism

Brief summary

To investigate changes in sclerostin levels following acute post-thyroidectomy hypoparathyroidism

Detailed description

Female patients with thyroid disorders, referred to the Department of Head and Neck Surgery, at Metaxa Anti-Cancer Hospital of Piraeus, for total thyroidectomy. Based on the development of biochemical hypocalcemia (cCa \< 8.4 mg/dl), subjects were divided into 2 groups: Group A: without postsurgical hypoparathyroidism that served as controls and group B: subjects, with acute postsurgical hypoparathyroidism. Blood collections were performed in the morning after an overnight fast, in at least 3 different time points; preoperatively, 1st postoperative day and 7th postoperative day for the detrmination of sclerostin levels

Interventions

DRUGcalcium carbonate and alphacalcidol

treatment for hypocalcemia

Sponsors

University of Athens
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
FEMALE
Age
19 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Indication for total thyroidectomy

Exclusion criteria

* parathyroid disorders, chronic kidney disease (eGFR\< 60 ml/min), treatment with antiosteoporosis drugs, rheumatic disease and history of long term (\>1 month) or current corticosteroid use

Design outcomes

Primary

MeasureTime frameDescription
change in circulating serum sclerostin levels (pmol/L) during the observation period7 dayschange in circulating serum sclerostin levels (pmol/L)during the observation period

Secondary

MeasureTime frameDescription
the between groups difference in % changes of circulating sclerostin7 daysthe between groups difference in % changes of circulating sclerostin

Countries

Greece

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026