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QOL Following Parathyroid Surgery
This study is ongoing, but not recruiting participants.
Sponsored by: University of Wisconsin, Madison
Information provided by: University of Wisconsin, Madison
ClinicalTrials.gov Identifier: NCT00205452
  Purpose

The only established treatment for the complete resolution of hyperparathyroidism is the surgical removal of the affected glands. While proven as a means of resolving hyperparathyroidism, there have been no comprehensive preoperative and postoperative assessments to determine quality of life for patients undergoing minimally invasive vs. traditional parathyroid surgery. Quality of life will be assessed in subjects undergoing minimally invasive procedures and traditional procedures using a clinically validated survey. We will gather data one week preoperatively as well as one week and one year postoperatively then compare the survey results from the two study groups to each other. We will also compare the study groups to a control group consisting of patients undergoing thyroid surgery. Our ultimate goal is to clarify if minimally invasive parathyroid surgery techniques contribute to a higher patient quality of life as compared to traditional techniques.


Condition
Parathyroidectomy

Drug Information available for: Parathyroid
U.S. FDA Resources
Study Type: Observational
Study Design: Cross-Sectional, Case Control, Retrospective/Prospective Study
Official Title: Does Quality of Life Improve Following Minimally Invasive Parathyroid Surgery?

Further study details as provided by University of Wisconsin, Madison:

Estimated Enrollment: 200
Study Start Date: June 2003
  Eligibility

Ages Eligible for Study:   18 Years and older
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • parathyroidectomy

Exclusion Criteria:

  • subjects under the age of 18
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00205452

Locations
United States, Wisconsin
University of Wisconsin Hospital and Clinics
Madison, Wisconsin, United States, 53792
Sponsors and Collaborators
University of Wisconsin, Madison
Investigators
Principal Investigator: Herbert Chen, MD University of Wisconsin Medical School
  More Information

Study ID Numbers: 2003-164
Study First Received: September 13, 2005
Last Updated: September 13, 2005
ClinicalTrials.gov Identifier: NCT00205452  
Health Authority: United States: Food and Drug Administration

Study placed in the following topic categories:
Quality of Life

ClinicalTrials.gov processed this record on January 16, 2009