The Asthma Control Rate Achieved by Budesonide/Formoterol in Clinical Practice in China

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AstraZeneca

Status

Completed

Conditions

Asthma

Treatments

Other: without interventions

Study type

Observational

Funder types

Industry

Identifiers

NCT01785901
NIS-RCN-SYM-2012/1

Details and patient eligibility

About

This is a multi-centre, cross-sectional study planned to be conducted in China. The study aims to observe about 1500 asthma patients who have already received budesonide/formoterol combination treatment by physicians' determination and whose medications are aligned with the package insert of budesonide/formoterol approved in China.

Full description

The asthma control rate achieved by budesonide/formoterol in clinical practice in China.

Enrollment

1,502 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. Clinical diagnosis of asthma at least 6 months;
  2. Prescribed with budesonide/formoterol treatment at least 3 months before enrolled;
  3. Has used the same maintenance dose of budesonide/formoterol for at least 4 weeks before enrolled.

Exclusion criteria

  1. Participation in any clinical study within 3 months;
  2. Have COPD history/suspicious COPD;
  3. ≥ 10 pack years of smoking history
  4. Used any other asthma maintenance medication accompanied with budesonide/formoterol within 3 months before enrolled
  5. With asthma exacerbation (defined as asthma symptom deterioration resulting oral/rectal/parenteral GCS medication or emergency room treatment or hospitalisation) within 4 weeks before enrolled

Trial design

1,502 participants in 1 patient group

Target subject population 1500
Description:
Asthma patients who have already received the treatment of budesonide/formoterol by physicians' determination and whose medications are aligned with the package insert of budesonide/formoterol approved in China
Treatment:
Other: without interventions

Trial contacts and locations

11

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Data sourced from clinicaltrials.gov

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