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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00443833
Other study ID # 11-46-21
Secondary ID
Status Completed
Phase N/A
First received March 5, 2007
Last updated March 5, 2007
Start date January 2004
Est. completion date December 2005

Study information

Verified date March 2007
Source Ramathibodi Hospital
Contact n/a
Is FDA regulated No
Health authority Thailand: Ethical Committee
Study type Observational

Clinical Trial Summary

Thyrotoxic periodic paralysis (TPP) is characterized by episodes of reversible hypokalemia and weakness in thyrotoxic patients. It is commonly found in males of Asian descent and is also seen in individuals having Native American or Hispanic ancestry. Therefore genetic etiology has been hypothesized. This study, we aim to find the susceptibility genes that associate with TPP. Both candidate genes approach and genome wide association study have been conducted.


Description:

This study is a genetic association study. It included 50 cases of TPP patients and 80 cases of male, hyperthyroid patients who didn't have hypokalemia as a well characterized controls. After informed consent were obtained, genomic DNA from leukocyte were extracted. Pooled DNA were constructed and whole genome scan using 10K GeneChip microarray were genotyped on pooled genomic DNA.


Recruitment information / eligibility

Status Completed
Enrollment 80
Est. completion date December 2005
Est. primary completion date
Accepts healthy volunteers No
Gender Male
Age group 15 Years and older
Eligibility Inclusion Criteria:

TPP

- Hyperthyroid patients from any causes

- Evidence of hypokalemia (k<3.5 mg/dl)from intracellular shift (Urine K<15 mg/dl, TTKG<2)

- Episodic paralysis

Exclusion Criteria:

- Hypokalemia from GI or renal loss

Study Design

Observational Model: Case Control, Primary Purpose: Screening, Time Perspective: Cross-Sectional


Related Conditions & MeSH terms


Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Ramathibodi Hospital
See also
  Status Clinical Trial Phase
Active, not recruiting NCT02287363 - Genetic and Morphological Analysis of Thyrotoxic Periodic Paralysis N/A