Small-fiber Neuropathy in Chronic Kidney Disease

Sponsor
National Taiwan University Hospital (Other)
Overall Status
Unknown status
CT.gov ID
NCT01078857
Collaborator
(none)
120
1

Study Details

Study Description

Brief Summary

Neurological dysfunction is a common complication of late stage chronic kidney disease (CKD) and peripheral nerve system is often involved in such complication. Sensory disturbances such as paresthesia and hypoesthesia are the predominant symptoms in uremic polyneuropathy and it is traditionally thought the uremic polyneuropathy mainly involve large-diameter sensory nerves. However in uremic patients the abnormal thermal thresholds, the sensory symptoms like numbness, burning, paradoxical heat, cold or freezing, and pain, and the frequent symptoms of autonomic dysfunction suggest that small-fiber neuropathy should be a clinical entity in patients of CKD. But there are still few investigations with emphasis on the changes of small-fiber nerves in CKD, and little is known about the characteristics and mechanism of small-fiber neuropathy in CKD. Skin biopsy with evaluation of epidermal nerve density and the morphology of epidermal nerves and the subepidermal nerve plexus is an effective and minimally invasive test for assessment of small-fiber neuropathy. Contact heat evoked potential (CHEP) recording the brain responses evoked by contact heat stimuli on the skin is a non-invasive technique to investigate the thermo-nociceptive pathways mediated by small-fiber nerves. In the current study, we will use an integrated approach by combining the skin biopsy, quantitative sensory testing, autonomic function tests, and CHEP to investigate the pathological, psychophysical and physiological aspects of small-fiber neuropathy in patients of CKD. The aims of the current study is to address the following issues: (1) the changes of small fiber nerves in uremia and CKD of different stage; (2) the correlation of skin innervation with clinical manifestations, thermal thresholds, and autonomic function; (3) the influence of dialysis therapy, the type of dialysis therapy, or renal transplantation on the small fiber neuropathy in uremia; (4) the roles of blood chemical substances, metals, and endocrine profiles on the development of small-fiber neuropathy; (5) the relationship between the small-fiber neuropathy and pruritus or restless leg syndrome; and (6) the pathological and physiological correlates of painful symptoms by skin biopsy and CHEP in CKD related neuropathy. The results of the study will provide important insights in the understanding of the pathogenesis, and the prevention and new treatments of small-fiber neuropathy in CKD.

Condition or Disease Intervention/Treatment Phase
  • Other: Skin biopsy
N/A

Study Design

Study Type:
Interventional
Anticipated Enrollment :
120 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Primary Purpose:
Diagnostic
Official Title:
Small-fiber Neuropathy in Chronic Kidney Disease
Study Start Date :
Feb 1, 2009
Anticipated Primary Completion Date :
Aug 1, 2012

Outcome Measures

Primary Outcome Measures

  1. The pathology of skin biopsy [within 3 months after inclusion]

  2. Intraepidermal fiber density [within 3 months after inclusion]

  3. Autonomic function [within 3 months after inclusion]

Secondary Outcome Measures

  1. Function of small-fiber sensory nerve [within 3 months after inclusion]

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • The patients should fulfill the criteria of CKD according to renal function study and the patients of end-stage renal disease should receive regular dialysis therapy and follow-up at outpatient clinics.

  • For disease comparison, patients with peripheral neuropathy of variable etiologies will also be recruited.

Exclusion Criteria:
  • Poor control DM,

  • Severe heart failure,

  • Bleeding tendency,

  • Severe lung disease with respiratory distress,

  • Severe infection,

  • Alcoholism,

  • Amyloidosis,

  • Poor wound healing history.

Contacts and Locations

Locations

Site City State Country Postal Code
1 National Taiwan University Hospital Taipei Taiwan 10002

Sponsors and Collaborators

  • National Taiwan University Hospital

Investigators

  • Study Director: Sung-Tsang Hsieh, National Taiwan University Hospital

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
, ,
ClinicalTrials.gov Identifier:
NCT01078857
Other Study ID Numbers:
  • 200812088R
First Posted:
Mar 2, 2010
Last Update Posted:
Mar 2, 2010
Last Verified:
Feb 1, 2010

Study Results

No Results Posted as of Mar 2, 2010