DrugLib.com — Drug Information Portal

Rx drug information, pharmaceutical research, clinical trials, news, and more



Glycyrrhetinic Acid-Effect on Serum Potassium and Insulin Resistance in Dialysis Patients

Information source: University Hospital Inselspital, Berne
Information obtained from ClinicalTrials.gov on October 19, 2009
Link to the current ClinicalTrials.gov record.

Condition(s) targeted: End Stage Renal Disease

Intervention: oral 18B Glycyrrhetinic acid versus placebo (Drug)

Phase: Phase 2

Status: Recruiting

Sponsored by: University Hospital Inselspital, Berne

Official(s) and/or principal investigator(s):
Felix J Frey, Prof, Principal Investigator, Affiliation: Department of Nephrology and Hypertension, University hospital of Berne

Overall contact:
Stefan Farese, MD, Phone: + 41 31 632 31 44, Email: stefan.farese@insel.ch

Summary

Background: 18B Glycyrrhetinic acid (active compound of Licorice) decreases serum potassium via enhanced renal potassium loss in healthy individuals and thereby inducing renal sodium retention and arterial hypertension. In dialysis patients this mechanism is disturbed and compensatory intestinal potassium secretion is enhanced. 18B Glycyrrhetinic acid is an inhibitor of 11B Hydroxysteroid dehydrogenase type 1 (11b HSD1). Inhibition of 11 b HSD1 offers a novel potential therapy to lower intracellular cortisol concentrations and thereby enhance insulin sensitivity.

Hypothesis: Glycyrrhetinic acid decreases serum potassium by enhanced intestinal excretion in dialysis patients and increases insulin sensivity by inhibition of 11b HSD

Methods: double blind, 6 month cross over trial comparing oral 18b Glycyrrhetinic acid with placebo in 24 nondiabetic dialysis patients.

Endpoints: predialytic serum potassium levels, insuline sensitivity assessed by fasting glucose and fasting insulin concentrations

Clinical Details

Official title: Glycyrrhetinic Acid-Effect on Serum Potassium and Insulin Resistance in Dialysis Patients

Study design: Treatment, Randomized, Double-Blind, Placebo Control, Crossover Assignment, Efficacy Study

Eligibility

Minimum age: N/A. Maximum age: N/A. Gender(s): Both.

Criteria:

Inclusion Criteria:

- dialysis patients (>3 months)

Exclusion Criteria:

- diabetics

- hospital stay in the last 4 weeks

Locations and Contacts

Stefan Farese, MD, Phone: + 41 31 632 31 44, Email: stefan.farese@insel.ch

Department of nephrology and hypertension, University hospital of berne, Berne 3010, Switzerland; Recruiting
Stefan Farese, MD, Phone: +41 31 631 31 44, Email: stefan.farese@insel.ch
Felix J Frey, Prof, Principal Investigator
Additional Information

Starting date: August 2006
Ending date: August 2007
Last updated: October 5, 2006

Page last updated: October 19, 2009

-- advertisement -- The American Red Cross
We comply with
HONcode standard.
Verify here.
Home | About Us | Contact Us | Site usage policy | Privacy policy

All Rights reserved - Copyright DrugLib.com, 2006-2009