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The assessment of microvascular alterations in renal-pancreas transplant recipients before and after transplantation.

The assessment of microvascular alterations in renal-pancreas transplant recipients before and after transplantation. - OPS-2

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON33101
Enrollment
15
Registered
2009-11-24
Start date
2010-03-23
Completion date
Unknown
Last updated
2024-11-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

diabetic nephropathy kidney-pancreas transplantation

Interventions

None listed

Sponsors

Leids Universitair Medisch Centrum
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: 1. Age: 18 -70 years 2. Female or male 3. Kidney-pancreas transplantation 4. Patients must be able to adhere to the study visit schedule and protocol requirements. 5. Patients must be able to give informed consent and the consent must be obtained prior to any study procedure.

Exclusion criteria

Exclusion criteria: 1. Patients with evidence of active infection or abcesses 2. Patients suffering from hepatic failure. 3. Patients suffering from an active autoimmune disease 4. Patients with epilepsy 5. Malignancy (including lymphoproliferative disease) within the past 2-5 years (except for squamous or basal cell carcinoma of the skin that has been treated with no evidence of recurrence). 6. Subjects who currently have an active opportunistic infection (e.g., herpes zoster [shingles], cytomegalovirus (CMV), Pneumocystis carinii (PCP), aspergillosis, histoplasmosis, or mycobacteria other than TB)

Design outcomes

Primary

MeasureTime frame
Non- invasive assessment of microvascular structure in diabetic nephropathy patients before and after kidney-pancreas transplantation.

Secondary

MeasureTime frame
1.Does kidney-pancreas transplantation improve microvascular damage assessed by OPS? 2.Does OPS correlate with serum and urine markers for fibrosis and endothelial dysfunction in these patients?

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)