The Application of Rapid PTH Test Paper in Operation of Hyperparathyroidism
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|ClinicalTrials.gov Identifier: NCT03434067|
Recruitment Status : Unknown
Verified September 2018 by Bo Wang,MD, Fujian Medical University.
Recruitment status was: Recruiting
First Posted : February 15, 2018
Last Update Posted : September 18, 2018
|Condition or disease|
|Hyperthyroidism Thyroidectomy PTH Immunochromatographic|
|Study Type :||Observational [Patient Registry]|
|Estimated Enrollment :||90 participants|
|Target Follow-Up Duration:||6 Months|
|Official Title:||The Application of Rapid PTH Test Paper in Operation of Hyperparathyroidism|
|Actual Study Start Date :||January 1, 2018|
|Actual Primary Completion Date :||June 30, 2018|
|Estimated Study Completion Date :||December 30, 2018|
Patients diagnosed with primary hyperparathyroidism are prepared for parathyroid surgery. PTH test paper is used addtional at the time point according to Miami principle
Patients diagnosed with Secondary hyperthyroidism are prepared for parathyroid surgery. PTH test paper is used addtional at the time point according to Miami principle
Patients diagnosed with unilateral thyroid benign tumor were prepared for unilateral thyroidectomy. PTH test paper is used addtional at postoperation
thyroidectomy and bilateral CCD
Patients diagnosed with bilateral thyroid carcinoma were prepared to undergo total thyroidectomy and bilateral central clearing.PTH test paper is used addtional at postoperation
- Serum PTH [ Time Frame: 0 minutes, 15 minutes, 1 hour and 24 hours post operation ]Routine serum PTH test, using immunoluminescence.
- Serum calcium [ Time Frame: 0 minutes, 15 minutes, 1 hour and 24 hours post operation ]Routine serum electrolyte detection.
- PTH test paper [ Time Frame: 0 minutes, 15 minutes, 1 hour and 24 hours post operation ]PTH test paper test for blood
Biospecimen Retention: Samples Without DNA
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT03434067
|Contact: wenxin zhao, email@example.com|
|Contact: bo wang, firstname.lastname@example.org|
|Study Chair:||wen-xin zhao, md||Fujian Medical University Union Hospital|