Clinical Trials Logo

Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT02528422
Other study ID # MY-1-2014
Secondary ID 2014-004496-23
Status Recruiting
Phase Phase 1
First received August 17, 2015
Last updated August 18, 2015
Start date May 2015
Est. completion date January 2018

Study information

Verified date August 2015
Source Regional Hospital Holstebro
Contact My ES Malmberg
Phone +4578436588
Email mymalmbe@rm.dk
Is FDA regulated No
Health authority Denmark: Danish Health and Medicines Authority
Study type Interventional

Clinical Trial Summary

Ghrelin (growth hormone release inducer) is produced in the stomach. The active form of Ghrelin is Acyl-Ghrelin. Acyl-Ghrelin stimulates the Ghrelin receptors. Ghrelin receptors are detected in the distal tubules in mice and animal studies have shown that Ghrelin increases the absorption of sodium in the renal tubules. Ghrelin infusion directly into the renal artery of rats increased sodium reabsorption in the distal nephron, presumably via the epithelial sodium channels (ENaC).

The purpose of the study is to measure the acyl-ghrelin induced effects on GFR, tubular transport of sodium and water in different nephron segments and central and peripheral blood pressure in a randomized, cross-over, single-blind, placebo-controlled dose-response study.


Recruitment information / eligibility

Status Recruiting
Enrollment 15
Est. completion date January 2018
Est. primary completion date January 2018
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 18 Years to 40 Years
Eligibility Inclusion Criteria:

- Age 18-40 years,

- BMI 18,5-30kg/m2,

- women must use contraception.

Exclusion Criteria:

- Tobacco smoking,

- substance abuse,

- consumption of more than 7 units of alcohol/week for women and more than 14 units/week for men,

- medical treatment except for contraception,

- pregnancy or nursing,

- allergy to acyl-ghrelin,

- significant clinical signs of heart-, lung-, liver-, kidney-, endocrine-, brain- or neoplastic disorders,

- clinically significant abnormal findings in screening blood samples,

- urine sample or ECG,

- office blood pressure over 140/90 mmHg,

- donation of blood within 1 month of the first day of investigation.

Study Design

Allocation: Randomized, Endpoint Classification: Pharmacokinetics/Dynamics Study, Intervention Model: Crossover Assignment, Masking: Single Blind (Subject), Primary Purpose: Basic Science


Related Conditions & MeSH terms


Intervention

Drug:
Acyl-Ghrelin


Locations

Country Name City State
Denmark Department of Medical Research, Regional Hospital Holstebro Holstebro

Sponsors (2)

Lead Sponsor Collaborator
Erling Bjerregaard Pedersen University of Aarhus

Country where clinical trial is conducted

Denmark, 

Outcome

Type Measure Description Time frame Safety issue
Primary Fractional sodium excreation (FENa) Measurement of FENa at baseline and after Acyl-Ghrelin injection 5-6 Hours No
Secondary Renal function Measurement of GFR, FEK and CH20 at baseline and after Acyl-Ghrelin injection 5-6 Hours No
Secondary Water and sodium transport Measurement of u-AQP2, u-NCC , u-NKCC -2 and u-ENaC at baseline and after Acyl-Ghrelin 5-6 Hours No
Secondary Vasoactive hormones Measurement of p-BNP , PRC, p-AngII , p-Aldo and p-AVP at baseline and after Acyl-Ghrelin 5-6 Hours No
Secondary Blood pressure Measurement of Central blood pressure, PWV, AIx and Peripheral blood pressure at baseline and after Acyl-Ghrelin 5-6 Hours No