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OpenTrials
Completed

NCT Number: NCT00963144

Diagnosis and Response to Treatment Using a Reliable Gastroesophageal Reflux Disease (GERD) Questionnaire: An In Clinical Practice Study

The purpose of the study is to determine the applicability and utility of Gerd Q in the diagnosis of GERD and in the assessment of treatment response.

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Key information

Age range

18 year–79 year

Sex eligibility

All sexes

Study type

Observational

Primary location

Research Site, Kuala Lumpur, Malaysia

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Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Patients of either gender aged between 18-79 years of age
  • Patients must be having symptoms of gastroesophageal reflux disease

Exclusion criteria

  • None

Treatment and study plan

Primary outcomes

  1. To determine the applicability and utility of Gerd Q in the diagnosis of GERD and assessment of treatment response

    Time frame: The applicability and utility of the Gerd Questionnaire will be done on 2 vists- Day 1 and Day 30

Secondary outcomes

  1. To assess and monitor the treatment response of patients diagnosed with GERD

    Time frame: The monitoring and assessment of treatment response using the Gerd Questionnaire will be done on 2 vists-Day 1 and Day 30

Sponsors and collaborators

Lead sponsor

AstraZeneca

Industry

Registry information

Official study title

Diagnosis and Response to Treatment Using a Reliable Gerd Questionnaire-an In Clinical Practise Study

Acronym: GQS

Important dates

Study start
2009
Primary completion
2009
Study completion
2009
First posted
Aug 21, 2009
Registry last updated
Oct 21, 2010

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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