Resources

Participant Informed Consent Forms 

CKD consent

Consent form to join the KPMP research study for CKD participants.

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AKI consent

Consent form to join the KPMP research study for AKI participants.

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AKI surgical consent

Consent form to join the KPMP research study for AKI participants undergoing a surgical procedure.

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KPMP Research Protocols

All research conducted by the KPMP consortium sites is done so according to a plan (a protocol). These protocols provide detailed guidelines for conducting a study and illustrate what will be done within a study by explaining each essential part of it and how it is carried out. In other words, protocols help researchers explain what they want to learn and how they’ll carry out their work.

All KPMP protocols are reviewed and revised periodically as the consortium adds new techniques or learns things that warrant updating our process.

Operational Protocols

 

Clinical protocol

Operational procedures for the overall KPMP study.

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Recruitment Site protocols 

Biospecimen protocol

Operational procedures for the collection, handling, and storage of participant biospecimens.

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Pathology protocol

Operational procedures for the collection, handling, processing, preservation, and transport of the renal biopsy cores.

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Recruitment site protocol

Operational procedures for patient recruitment, enrollment, and retention; biopsy collection and shipment; and data quality management.

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Tissue Interrogation Sites 

Tissue interrogation sites protocols

Operational procedures of the tissue interrogation sites for processing the renal biopsy tissue using various -omics technologies.

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