The Effect of Bariatric Surgery on Peripheral Nerve Function and Axonal Regeneration (BAR)
|
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details. |
| ClinicalTrials.gov Identifier: NCT02218866 |
|
Recruitment Status :
Completed
First Posted : August 18, 2014
Last Update Posted : April 10, 2018
|
- Study Details
- Tabular View
- No Results Posted
- Disclaimer
- How to Read a Study Record
| Condition or disease |
|---|
| Peripheral Neuropathy Obesity |
Peripheral neuropathy causes progressive injury to the longest nerves of the body, starting in the toes, then progressing slowly up the leg. Neuropathy often causes pain, numbness, and weakness if the feet and can lead to reduced mobility, foot ulcers, and even amputation. The most common cause is diabetes, but work at the University of Utah finds that prediabetes and other consequences of obesity, including abnormal cholesterol levels, may be associated with neuropathy. Research has shown that these risk factors may damage nerves and interfere with the ability of nerves to grow back after an injury.
This study aims to
- characterize peripheral nerve function and cutaneous nerve structure in obese bariatric surgery candidates;
- evaluate peripheral nerve regeneration capacity (and other nerve function measures) before and after bariatric surgery in obese subjects with no or mild neuropathy;
- examine the relationship between ectopic lipid accumulation, lipotoxic mediators, neuropathy and regeneration capacity in surgical candidates before and one year after surgery.
| Study Type : | Observational |
| Actual Enrollment : | 205 participants |
| Observational Model: | Case-Control |
| Time Perspective: | Prospective |
| Official Title: | The Effect of Bariatric Surgery on Peripheral Nerve Function and Axonal Regeneration |
| Study Start Date : | January 2012 |
| Actual Primary Completion Date : | December 31, 2017 |
| Actual Study Completion Date : | December 31, 2017 |
| Group/Cohort |
|---|
|
Group 1
All participants will be examined by a neurologist to test sensation, reflexes, and strength and complete a few questionnaires. Tests will be performed to measure nerve function and small punch skin biopsies will be taken to assess nerve fiber density. Blood and urine tests will measure various markers of interest. Participants will be seen before and after their bariatric surgery.
|
|
Group 2
In addition to the procedures described for Group 1, participants in Group 2 will have the following procedures:
|
|
Group 3
Group 3 will comprise of individuals who are not overweight. Participants in this group will undergo a similar evaluation to Group 2.
|
- Change in reinnervation capacity [ Time Frame: 4 - 1 months prior to bariatric surgery, compared to 9 - 12 months after surgery ]
- Change in Utah Early Neuropathy Scale (UENS) [ Time Frame: Baseline to 12 months after bariatric surgery ]
- Change in Nerve Conduction Study measures [ Time Frame: Baseline to 12 months after bariatric surgery ]Nerve Conduction Study is a procedure routinely used in the diagnosis of neuropathy. Measures will include Sural sensory and Peroneal motor amplitudes and conduction velocities.
- Change in nerve fiber density [ Time Frame: Baseline to 12 months after bariatric surgery ]
Biospecimen Retention: Samples With DNA
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.
| Ages Eligible for Study: | 18 Years to 80 Years (Adult, Older Adult) |
| Sexes Eligible for Study: | All |
| Accepts Healthy Volunteers: | Yes |
| Sampling Method: | Non-Probability Sample |
Inclusion Criteria:
- Age 18-80 years old
- Subjects must fulfill criteria for bariatric surgery.
Exclusion Criteria:
- History of foot ulceration or neurogenic arthropathy
- Family history of non-diabetic neuropathy in a first-degree family member.
- Presence of any disease known to be associated with peripheral neuropathy including but not limited to vitamin deficiency, toxin exposure, paraproteinemia, heavy alcohol use, hepatitis C, HIV.
- Coumadin use.
- Inability to understand or cooperate with the procedures of the trial.
- Known history of sensitivity to capsaicin products.
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): NCT02218866
| United States, Utah | |
| University of Utah | |
| Salt Lake City, Utah, United States, 84132 | |
| Principal Investigator: | A. Gordon Smith, MD | University of Utah |
| Responsible Party: | Gordon Smith, Professor, University of Utah |
| ClinicalTrials.gov Identifier: | NCT02218866 |
| Other Study ID Numbers: |
BAR-UofU |
| First Posted: | August 18, 2014 Key Record Dates |
| Last Update Posted: | April 10, 2018 |
| Last Verified: | August 2016 |
|
Bariatric surgery Obesity Neuropathy |
|
Peripheral Nervous System Diseases Neuromuscular Diseases Nervous System Diseases |

