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Investigating the effect of Medroxyprogesterone on blood gases and short-term outcomes in COPD patients undergoing Non-Invasive Ventilation(NIV)

Investigating the effect of Medroxyprogesterone on blood gases and short-term outcomes in COPD patients undergoing Non-Invasive Ventilation(NIV)

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20210730052016N2
Enrollment
80
Registered
2025-10-06
Start date
2025-10-21
Completion date
Unknown
Last updated
2025-10-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Chronic Obstructive Pulmonary Disease. Chronic obstructive pulmonary disease with (acute) exacerbation

Interventions

Intervention 1: Intervention group: In the intervention group, patients with severe COPD who require NIV will receive standard treatments including bronchodilators, systemic corticosteroids (prednisol

Sponsors

Hamedan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
30 Years to 80 Years

Inclusion criteria

Inclusion criteria: age between 30 and 80 years , patients with COPD experiencing an exacerbation (defined as having at least two of the three following criteria: increased dyspnea, increased sputum volume, and a change in sputum color to purulent sputum), need for NIV providing written informed consent to participate in the study

Exclusion criteria

Exclusion criteria: • Need for mechanical ventilation at the time of admission • History of cerebrovascular disease • History of myocardial infarction and stroke

Design outcomes

Primary

MeasureTime frame
Changes in blood pH. Timepoint: Before treatment - 3 days after treatment - 5 days after treatment. Method of measurement: Arterial blood sampling and gas analyzer device.;PCO2. Timepoint: Before treatment - 3 days after treatment - 5 days after treatment. Method of measurement: Arterial blood sampling and gas analyzer device.;O2 saturation. Timepoint: Before treatment - 3 days after treatment - 5 days after treatment. Method of measurement: Pulse oximeter.

Secondary

MeasureTime frame
Severity of dyspnea. Timepoint: Before treatment - 3 days after treatment - 5 days after treatment. Method of measurement: With the BORG scale.;Duration of need for NIV. Timepoint: Throughout the patient’s hospital stay. Method of measurement: Duration of NIV use for each patient.;Duration of hospital stay. Timepoint: Throughout the patient’s hospital stay. Method of measurement: Duration of stay for each patient.;Intubation. Timepoint: Throughout the patient’s hospital stay. Method of measurement: Patient’s clinical status and treatment decisions.;Admission to ICU. Timepoint: Throughout the patient’s hospital stay. Method of measurement: Patient’s clinical status and treatment decisions.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactZohreh Kahramfar

Hamedan University of Medical Sciences

kahramfar@umsha.ac.ir+98 81 3831 6246

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026