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Clinical Trials/NCT03676361
NCT03676361
Withdrawn
Phase 4

To Evaluate the Renal Tubular Function Pre and Post Nephrectomy in Living Donors

University of Kansas Medical Center1 site in 1 countryAugust 29, 2018
ConditionsKidney Damage
InterventionsDesmopressin

Overview

Phase
Phase 4
Intervention
Desmopressin
Conditions
Kidney Damage
Sponsor
University of Kansas Medical Center
Locations
1
Primary Endpoint
Percentage change in tubular function (urine osmolality measured in MOSMOL/K) pre and post nephrectomy as assessed through water deprivation and administration of desmopressin.
Status
Withdrawn
Last Updated
6 years ago

Overview

Brief Summary

The overall goals of this study are to demonstrate the change in renal tubular function in living donors pre and post nephrectomy at 6 months.

Detailed Description

The physiologic sequelae of living kidney donation are still poorly understood. Uni-nephrectomy from donation results in decreased number of glomeruli and research has shown that there is glomerular hyperfiltration and glomerular hypertrophy. Uni-nephrectomy also results in a decreased number of tubules, but there is not much data about possible tubular injury post donation and its long term effects on donors. Our overall hypothesis is that post uni-nephrectomy tubular function, measured by maximum urine concentration capacity, will be decreased and may be a more sensitive marker of kidney damage than standard tests, such as urine albumin, serum creatinine, estimated glomerular filtration rate (eGFR), or measured urine creatinine clearance (CrCl). The goal of this study is to evaluate the effect of uni-nephrectomy on renal tubular function and its potential in being an early and more sensitive marker in kidney injury when compared to standard tests.

Registry
clinicaltrials.gov
Start Date
August 29, 2018
End Date
April 26, 2019
Last Updated
6 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Pooja Budhiraja, MD

Assistant Professor

University of Kansas Medical Center

Eligibility Criteria

Inclusion Criteria

  • Adult ≥18 years of age, who has been evaluated and approved as a potential living donor by the multi-disciplinary committee. All donors undergo a standard medical, social, and psychological pre- donation assessment
  • Only patients who are able to sign their own consent form may be included in this study.
  • Subjects must be able and willing, in the investigator's opinion, to complete all study requirements.

Exclusion Criteria

  • Subjects denied for donation for any medical, social or surgical reason to be living donor.
  • Patients who are contraindicated or relatively contraindicated for DDAVP: a. patients with von Willebrand disease; b. Patients with habitual or psychogenic polydipsia; c. Patients with coronary artery insufficiency and/or hypertensive cardiovascular disease; d. Patients with conditions associated with fluid and electrolyte imbalance, such as cystic fibrosis, heart failure, and renal disorders; e. Patients predisposed to thrombus formation

Arms & Interventions

Desmopressin

All ten subjects will be evaluated pre and post nephrectomy at 6 months.

Intervention: Desmopressin

Outcomes

Primary Outcomes

Percentage change in tubular function (urine osmolality measured in MOSMOL/K) pre and post nephrectomy as assessed through water deprivation and administration of desmopressin.

Time Frame: 6 months

Tubular function is measured as maximal urine concentrating capacity reached after water deprivation and administration of desmopressin.

Secondary Outcomes

  • Sensitivity of urine albumin excretion when compared to change in tubular function, pre and post nephrectomy as measured in MCG/ML.(6 months)
  • Sensitivity of eGFR when compared to change in tubular function, pre and post nephrectomy as measured in mL/min.(6 months)
  • Sensitivity of serum creatinine when compared to change in tubular function, pre and post nephrectomy as measured in MG/DL.(6 months)

Study Sites (1)

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