Arthritis Clinical Trial
Official title:
A Pilot Study to Assess the Effects of Regulating Urine pH Levels for Alleviating Chronic Joint Pain
Verified date | May 2017 |
Source | Texas Tech University Health Sciences Center, El Paso |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
This study aims to determine the causal relationship between regulating urine pH levels between 7.0 and 7.5 and decreasing chronic joint pain. The investigators hypothesize that maintenance of an alkaline urinary pH will result in a decrease in personally reported levels of chronic joint pain using a citrate treatment regimen.
Status | Withdrawn |
Enrollment | 0 |
Est. completion date | March 2012 |
Est. primary completion date | March 2012 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 21 Years to 80 Years |
Eligibility |
Inclusion Criteria: 1. Presence of joint pain of perceived inflammatory and non-inflammatory origin for more than six months. More specifically: - Subjects with osteoarthritis (OA) of the knee will be preferred for inclusion in this study. - Subjects with other joint pain history will be included pursuant on approval from Dr. Miller or Dr. Pema. 2. Age 21 to 80 years old and otherwise in good health (excluding the joint pain). 3. Able to understand and comply with the assigned urine alkalinization instructions. 4. Has a working and reliable telephone number for continued contact as necessary during the study. 5. Ability to obtain X-rays of the affected joint. Imaging of the painful joint will be necessary at the beginning of the study for baseline considerations; if images from the last 6 months are available, no new imaging would be necessary. 6. Ability to obtain lab tests (Complete Blood Count and Comprehensive Metabolic Panel) or can obtain documentation of recent lab tests that have been taken within one month prior to enrollment. 7. Ability to obtain lab tests at 3 and 6 months during participation in the study. Exclusion Criteria: 1. Presence of joint pain with known joint osseous changes. 2. Pregnant or lactating women will not be enrolled in the study. 3. Positive medical history of: - Diabetes - Neuropathies - Gout - Psychiatric diseases and conditions, including anxiety, depression, PTSD, distress - Psychosocial abnormalities - Dementia or other memory disturbances - Alcoholism or substance abuse - Renal failure and/or abnormal renal function (kidney disease or dysfunction). Specifically, Creatinine (Creat) values that are over 1.2mg/dL and Urea Nitrogen (BUN) values that are over 22mg/dL are considered abnormal. - No history of cardiovascular disease, intestinal angina or arrhythmias - No history of sodium restrictions - Pt. should not be taking medications which produce pain such as angiotensin converting enzyme (ACE) inhibitors and Statins (Lisinopril, Quinapril, Ramipril) 4. Does not have reliable telephone communication. 5. Does not have the ability to obtain an X-ray and does not have the ability to obtain documentation of a recent X-ray within the last six months. 6. Does not have the ability to obtain lab tests (Complete Blood Count and Comprehensive Metabolic Panel) and does not have the ability to obtain documentation of recent lab tests that have been taken within one month prior to enrollment. 7. Does not have the ability to obtain lab tests at 3 and 6 months during participation in the study. |
Country | Name | City | State |
---|---|---|---|
United States | Department of Anesthesiology; Texas Tech University Health Sciences Center; Paul L. Foster School of Medicine | El Paso | Texas |
Lead Sponsor | Collaborator |
---|---|
Texas Tech University Health Sciences Center, El Paso |
United States,
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* Note: There are 17 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Pre-and post test pain rating | At the beginning of the study, during office visits, and at the end of the study, subjects will be asked to visually and numerically rate their pain levels. | Six months | |
Primary | Change in Urine pH from baseline | Subject's daily self-report of this measure will be provided to study investigator at each office visit. | Six months | |
Primary | Changes in lab results (routine blood work) from baseline | Assessed at the beginning, middle (3 months) and end of the six month study. | Six months. | |
Primary | Change in amount of alkalization medication taken daily | Subject's daily self-report of this measure will be provided to study investigator at each office visit. | Six months | |
Secondary | Daily food and beverage intake | Subject's daily self-report of this measure will be provided to the study investigator at each office visit. | Six months |
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