Last updated: 11/07/2018 19:22:52

Determination of the Efficacy of GR33343G (50mcg Twice Daily) Administered From a Metered Dose Inhaler in the Elderly.

GSK study ID
SLGT12
Clinicaltrials.gov ID
Not applicable
EudraCT ID
Not applicable
EU CT Number
Not applicable
Trial status
Study complete
Study complete
Overview
Eligibility
Locations
Study documents
Results summary
Plain language summaries
Additional information

Trial overview

Official title: Determination of the Efficacy of GR33343G (50mcg Twice Daily) Administered From a Metered Dose Inhaler in the Elderly.
Trial description: Determination of the Efficacy of GR33343G (50mcg Twice Daily) Administered From a Metered Dose Inhaler in the Elderly.
Primary purpose:
Not applicable
Trial design:
Not applicable
Masking:
Not applicable
Allocation:
Not applicable
Primary outcomes:
Not applicable
Secondary outcomes:
Not applicable
Interventions:
Not applicable
Enrollment:
Not applicable
Primary completion date:
Not applicable
Observational study model:
Not applicable
Time perspective:
Not applicable
Clinical publications:
Starke ID Luce P. The efficacy and safety of inhaled salmeterol 50 mcg bd in older patients with reversible airflow obstruction. Age and Ageing 1996;25(1):67-71.
Medical condition
Asthma
Product
salmeterol
Collaborators
Not applicable
Study date(s)
May 1989 to January 1990
Type
Not applicable
Phase
2

Participation criteria

Sex
Not applicable
Age
Not applicable
Accepts healthy volunteers
Not applicable

Trial location(s)

This study does not involve prospective enrollment of participants.

Study documents

Scientific result summary
Available language(s): English

If you wish to request for full study report, please contact - [email protected]

Results overview

Not applicable

Recruitment status
Study complete
Actual primary completion date
Not applicable
Actual study completion date
1990-25-01

Plain language summaries

Plain language summaries of clinical trial results for Phase 2-4 clinical trials that were initiated on or after January 2022 will be posted by GSK within one year following study completion.

Additional information about the trial

Not applicable
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