Menstrual Differences in Airway Inflammation in Asthma

This study has been completed.
Sponsor:
Information provided by (Responsible Party):
The University of Texas, Galveston
ClinicalTrials.gov Identifier:
NCT00584441
First received: December 20, 2007
Last updated: February 11, 2013
Last verified: February 2013

December 20, 2007
February 11, 2013
September 2007
February 2010   (final data collection date for primary outcome measure)
To evaluate menstrual-related changes in airway inflammation of asthma patients with and without premenstrual worsening of symptoms. [ Time Frame: 3 months ] [ Designated as safety issue: No ]
Same as current
Complete list of historical versions of study NCT00584441 on ClinicalTrials.gov Archive Site
  • To examine the effect of sex hormones in airway inflammation [ Time Frame: 3 months ] [ Designated as safety issue: No ]
  • To examine the effect of oral contraceptive pills on airway inflammation [ Time Frame: 3 months ] [ Designated as safety issue: No ]
  • To assess the cyclical changes in airway inflammation as measured by -Fractional exhaled Nitric Oxide (FeNO), -Exhaled Breath Condensate (EBC) pH and -Serum eosinophil cationic protein (ECP), in asthmatic women with and without premenstrual asthma. [ Time Frame: 3 months ] [ Designated as safety issue: No ]
  • To analyze the association of between serum estradiol and progesterone levels and the variation in airway inflammation, airflow limitation and asthma symptoms [ Time Frame: 3 months ] [ Designated as safety issue: No ]
  • To study the effect of oral contraceptives on airway inflammation by measuring serum and exhaled inflammatory indices [ Time Frame: 3 months ] [ Designated as safety issue: No ]
Same as current
Not Provided
Not Provided
 
Menstrual Differences in Airway Inflammation in Asthma
Menstrual Differences in Airway Inflammation in Asthma

Asthma is a chronic inflammatory lung disease characterized by airway hyper-responsiveness and reversible airway obstruction. Over the last decade, the prevalence of asthma is on the rise and it disproportionately affects more women than men. As much as 40% of women with asthma are known to have worsening of asthma symptoms and lung function prior to menstruation. This syndrome is being increasingly recognized as premenstrual asthma (PMA). The pathologic differences in female asthmatics with and without this syndrome are not known. The evidence regarding the role of sex hormones has been contradicting. We propose an observational cohort study to examine the changes in airway inflammation in women with asthma in relation to their menstrual cycle and their association with sex hormone levels. In addition we will include women on oral contraceptives to determine their effect on airway inflammation and asthma symptoms.

We hypothesis that:

  • Women with premenstrual asthma will show increased indices of airway inflammation in various phases the monthly menstrual cycle.
  • In women with premenstrual asthma, a change in serum estradiol/progesterone ratio during the late luteal phase is associated with worsening of airway inflammation, air flow limitation and asthma symptoms.
  • The use of oral contraceptives is associated with suppression of the cyclical changes in airway inflammation due to lack of fluctuations in estradiol and progesterone levels.

Recruited subjects will be asked to record asthma symptom scores, morning Peak Expiratory Flow Rate (m-PEFR) and rescue asthma medication (β2-agonist) used daily during the one month screening period to identify women with and without pre-menstrual asthma. Asthmatic women with regular menstrual cycles will be evaluated in their follicular phase (days 5-8) and luteal phase (days 21-24) and women on oral contraceptive pills (OCP) will be evaluated on days 9-12 of their OCP cycle and during the days 25-28, off of OCP consecutively for a 2-month period.

Not Provided
Observational
Observational Model: Case Control
Time Perspective: Prospective
Not Provided
Retention:   Samples Without DNA
Description:

Serum Eosinophil Cationic Protein (ECP) samples will be obtained. The 5ml blood samples for measuring ECP levels will be collected in silica gel-containing tubes. After centrifuging, the supernatant will be frozen and ECP levels will bemeasured using an ELISA kit

Non-Probability Sample

Females diagnosed with asthma, with either regular menstral cycles or on monophasic oral contraceptives, with or without pre-mentstual asthma symptoms

Asthma
Not Provided
  • 1
    Women with pre-menstrual asthma (PMA): As defined by a 20% or more fall in PEFR and / or change by 20% or more of daily symptom score.
  • 2
    Women without pre-menstrual asthma
  • 3
    Women on oral contraceptives
Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Completed
6
February 2010
February 2010   (final data collection date for primary outcome measure)

Inclusion Criteria:

  • With diagnosis of Asthma (ICD-9 Code 493)
  • Requiring low to moderate dose inhaled corticosteroids for control.
  • With Pre-bronchodilator FEV1 ≥50% and ≤90% of predicted normal
  • With a positive bronchodilator response
  • Non smoker or Ex-smoker (Quit >1 year ago)
  • Regular menstrual cycle (24-35 days cycle)
  • With and without OCP use
  • Constant dose of asthma maintenance medication for at least 30 days prior to enrolment

Exclusion Criteria:

  • Recent use of systemic steroids (<30 days)
  • Severe Asthma (FEV1 <50% or frequent exacerbations or systemic steroid dependence)
  • Negative bronchodilator response
  • Current Smoker
  • Irregular Menses or postmenopausal
  • Positive pregnancy test
  • Use of hormonal contraceptives other than monophasic OCPs
  • Exacerbation or Respiratory Infection or antibiotic use within the last 30 days
Female
18 Years to 50 Years
Yes
Contact information is only displayed when the study is recruiting subjects
United States
 
NCT00584441
07-256
No
The University of Texas, Galveston
The University of Texas, Galveston
Not Provided
Principal Investigator: Anandhi T Murugan, MD, MPH University of Texas
The University of Texas, Galveston
February 2013

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP