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Completed

NCT Number: NCT01786616

Polymorphism of beta2-adrenoceptor and Regular Use of Formoterol in Asthma

Polymorphism at codon 16 of the beta2-adrenoceptor (beta2-AR) affects the responsiveness to salmeterol in asthmatics. Data concerning formoterol are more controversial in literature. The aim of this study was to verify whether homozygote for arginine-16 (ArgArg16) and homozygote for glycine-16 (GlyGly16) genotypes differently influence the long-term responsiveness to formoterol.

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Key information

Age range

18 year–60 year

Sex eligibility

All sexes

Study type

Observational

Primary location

Catholic University, Pneumology Unit

Rome, 00168, Italy

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Mild to moderate asthma
  • Stable clinical conditions

Exclusion criteria

  • Smokers
  • Current therapy with oral steroids
  • Exacerbations within the past 3 months

Treatment and study plan

Formoterol

Drug

Primary outcomes

  1. Peak Expiratory Flow (PEF) variability

    Time frame: PEF has been monitorized during the 4-week treatment period

Secondary outcomes

  1. Forced Expiratory Volume in 1 sec (FEV1) slope of the dose-response curve to salbutamol

    Time frame: At the end of the 4-week treatment period

Sponsors and collaborators

Lead sponsor

Catholic University, Italy

Other

Registry information

Official study title

Polymorphism of beta2-adrenoceptor and Regular Use of Formoterol in Asthma: Preliminary Results

Important dates

Study start
2005
Primary completion
2010
First posted
Feb 8, 2013
Registry last updated
Feb 8, 2013

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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