Kidney, Polycystic, Autosomal Dominant Clinical Trial
Official title:
Evaluation and Treatment of Chronic Pain in Autosomal Dominant Polycystic Kidney Disease
| Verified date | October 2017 |
| Source | Mayo Clinic |
| Contact | n/a |
| Is FDA regulated | No |
| Health authority | |
| Study type | Interventional |
We will enroll 20 patients to evaluate the effectiveness of a new operation known as videothoracoscopic splanchnicectomy (VSPL) for management of chronic kidney pain. This study is being done to test if this procedure is effective in controlling chronic kidney pain.
| Status | Completed |
| Enrollment | 18 |
| Est. completion date | January 2016 |
| Est. primary completion date | January 2016 |
| Accepts healthy volunteers | No |
| Gender | All |
| Age group | 18 Years and older |
| Eligibility |
Inclusion Criteria: - 18 years or older - Diagnosis of Autosomal Dominant Polycystic Kidney Disease (ADPKD) - History of debilitating kidney pain for at least 6 month. Other methods of pain management will have been appropriately considered and used when feasible and indicated. - Patient fit for general anesthesia - Must be able to travel to Mayo Clinic Rochester for 3 visits - Must be able to cover the cost of the surgery and post operative care. Exclusion Criteria: - Pregnant women (must have a confirmed negative pregnancy test) - Nursing women - Creatinine > 3mg/dl, or hemodialysis dependent - Cancer and other major systemic diseases that could prevent follow-up or data interpretation - Neurologic or psychologic conditions preventing appropriate informed consent - Uncontrolled hypertension(SBP > 160; DBP >100) |
| Country | Name | City | State |
|---|---|---|---|
| United States | Mayo Clinic | Rochester | Minnesota |
| Lead Sponsor | Collaborator |
|---|---|
| Mayo Clinic | Polycystic Kidney Disease Foundation |
United States,
| Type | Measure | Description | Time frame | Safety issue |
|---|---|---|---|---|
| Primary | Improvement in pain control and quality of life | 2 yrs | ||
| Secondary | Changes in urine biomarkers compared to pre-operation values within patients will be compared. Changes in kidney volume, kidney cyst volume, and kidney blood flow before and after the operation will be studied. | 3 years |
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