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Comparison of the results of treatment of the primary parathyroid adenoma with surgery or ablation with ethanol.

Phase 3
Recruiting
Conditions
Benign parathyroid adenoma.
Benign neoplasm of parathyroid gland
D35.1
Registration Number
IRCT20210204050241N1
Lead Sponsor
Esfahan University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
120
Inclusion Criteria

Patients with symptomatic benign parathyroid adenoma confirmed by ultrasound, MIBI scan, and fine needle aspiration

Exclusion Criteria

Patients with MEN1 or MEN2 syndrome
Patients with suspected parathyroid malignant adenoma
Patients with secondary or tertiary hyperparathyroidism
Not willing to participate in the trial
GFR<30 ml/min/1.72 m2
age above 50

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Serum calcium level. Timepoint: Before the intervention, 24 hours, two weeks, three months, and six months after the intervention. Method of measurement: Blood sample tests.;Serum PTH level. Timepoint: Before the intervention, 24 hours, two weeks, three months, and six months after the intervention. Method of measurement: Blood sample tests.
Secondary Outcome Measures
NameTimeMethod
Adenoma recurrence (reoperation or re-injection of alcohol). Timepoint: Within 3 months and 6 months after the intervention. Method of measurement: Changes in serum calcium and parathyroid hormone levels after intervention.
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