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Status unknownNCT00763477ghrelinUpdated Jul 27, 2010

Ghrelin in Cystic Fibrosis

An interventional study of ghrelin in Cystic Fibrosis, sponsored by Papworth Hospital NHS Foundation Trust. Status unknown at 1 site in United Kingdom. Open to participants aged 18 Years to 80 Years. Per ClinicalTrials.gov, last updated 2010-07-27.

Sponsored by Papworth Hospital NHS Foundation Trust · Not applicable, Interventional, and Health services research

The sponsor has not verified this record recently (last verified Jul 2010), so the status shown — last known as Recruiting — may be out of date.
Phase
Not applicable
Study type
Interventional
Enrollment
20
Allocation
Randomized
Ages
18 Years to 80 Years
Sex
All
01

Study summary

Background to ghrelin Ghrelin is a naturally occurring hormone found in the blood which stimulates appetite. In healthy individuals, levels of ghrelin are high before a meal and falls afterwards. Previous studies have shown that giving ghrelin (by injection) to thin patients with renal failure and cancer increases their food intake. Furthermore, addition of ghrelin may also reduce inflammation within the body. Cystic Fibrosis (CF) is a genetic disease which frequently results in recurrent lung infections (leading to progressive inflammatory lung damage) and low body weight. Low body weight in CF is associated with increased lung infections, rapidly worsening lung function and a shortened life expectancy.

The researchers postulate that administration of extra ghrelin to CF patients with low body weight may increase food intake and reduce lung inflammation. If successful, this study might identify ghrelin as a potential therapy for CF patients to improve nutrition, decrease lung inflammation and thereby improve survival.

Read the detailed description

The purpose of this study is to investigate the role of a naturally occuring hormone called ghrelin on appetite, energy expenditure and immune function in patients with cystic fibrosis.

Theoretical framework:

Despite advances in the molecular understanding of the disease, life-expectancy in Cystic Fibrosis (CF) remains severely limited. Reduced body-weight is associated with increased inflammatory lung damage and is a major predictor of mortality in CF patients. Malnutrition is highly prevalent in the CF population and results from both poor food intake and excessive energy expenditure. A therapy which improves nutrition may therefore have a significant effect on the prognosis of this disease. Ghrelin is the only physiological circulating factor that is known to increase food intake. Administration of acylated ghrelin to humans increases both hunger and food intake and has been found to increase appetite in chronic disease states associated with anorexia and weight loss (such as cancer and chronic renal disease). From multiple animal and in vitro human studies, ghrelin also appears to have anti-inflammatory properties which would potentially benefit CF patients in whom a chronic inflammatory state promotes lung destruction, malnutrition and increases mortality. Ghrelin replacement may therefore improve nutrition and decrease the inflammatory burden in CF patients, leading to an improvement in life-expectancy. If ghrelin is identified as having an important pathophysiological role in CF it may lead to a future study of its efficacy as a therapeutic agent.

Design Methodology: The study has three sections:

  1. a cross sectional study of the levels of blood metabolic signals in participants with cystic fibrosis and healthy controls.
  2. a laboratory study of the effect of ghrelin on immune cells extracted from the blood of participants with cystic fibrosis and healthy controls
  3. a cross-over interventional study of repeated ghrelin administration in malnourished cystic fibrosis patients
02

Conditions studied

  • Cystic Fibrosis

Keywords

  • Cystic fibrosis
  • Weight
  • Appetite
  • Ghrelin
  • Cystic fibrosis with low BMI
03

In context

Cystic Fibrosis

1,581 studies on the registry are indexed under Cystic Fibrosis; 190 are open to participants now.

This study's planned enrollment of 20 is below the median of 36 across 1,034 interventional studies indexed under Cystic Fibrosis.

Browse Cystic Fibrosis studies →

Lead sponsor

Papworth Hospital NHS Foundation Trust is the lead sponsor of 62 studies on the registry; 8 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 80 Years
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • Cystic fibrosis
  • BMI \</=19 kg/m2

Exclusion criteria

Exclusion Criteria:

  • Needle phobia
  • Pulmonary infection requiring intravenous antibiotics in the past 2 weeks-
05

Study design

Phase
Not applicable
Primary purpose
Health services research
Allocation
Randomized
Intervention model
Crossover assignment
Masking
Triple (Participant, Care provider, Investigator)
Enrollment
20 participants (estimated)

Study arms

  • Placebo comparator
    saline injections

    Biological: ghrelin

Interventions

  • Biologicalghrelin

    subcutaneous injection

06

What researchers measure

Primary outcomes

  1. Appetite

    Time frame: 4 weeks

Secondary outcomes

  1. weight

    Time frame: 4 weeks

07

Study locations

1 of 1 sites recruiting
  • Papworth Hospital NHs Foundation Trust
    Cambridge, Cambridgeshire CB23 3RE, United Kingdom
    • Andres R Floto, BM BSc, PhD · Contact · andres.floto@papworth.nhs.uk · 01480 830541
    • Jane D Elliott, MPhil · Contact · 01480 364495
    • Andres Floto, MB BChir, PhD, FRCP · Principal investigator
    • Katie J Wynne, MB BChir, PhD, FRCP · Sub investigator
    Recruiting
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jul 27, 2010, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT00763477
Lead sponsor
Papworth Hospital NHS Foundation Trust
First posted
Oct 1, 2008
Start date
Apr 2010
Primary completion
Feb 2011 (estimated)
Completion
Apr 2011 (estimated)
Last update
Jul 27, 2010

Oversight

Data monitoring committee
Yes
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is status unknown, as verified in Jul 2010. You cannot join it, but the record below documents what was studied.

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