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The effect of low-dose oral Theophylline drug on active c serum protein level in patients with stable chronic obstructive pulmonary disease

The effect of low-dose oral Theophylline on serum HS-CRP in patients with stable COPD

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT138808182685N1
Enrollment
50
Registered
2009-12-05
Start date
2008-12-05
Completion date
Unknown
Last updated
2018-02-22

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 Bronchitis, Emphysema with FEV1<70

Interventions

Intervention 1: Placebo with dose of 200 mg every 12 hours for one month. Intervention 2: Theophylline tablets, 200 mg every 12 hours for one month.
Placebo
Treatment - Drugs
Placebo with dose of 200 mg every 12 hours for one month
Theophylline tablets, 200 mg every 12 hours for one month

Sponsors

Vice-chancellor for Research, Kurdistan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Inclusion criteria: stable COPD (no exacerbation in the past two months), FEV1/FVC ratio less than 70%. Exclusion criteria: no smoking history, FEV1 increased more than 200 cc or 12% after administration of 400 micrograms spray Salbutamol in spirometry, clinical or radiographic evidence of pneumonia, history of infectious disease such as tuberculosis, recent respiratory tract infections, bronchiectasis, acute or chronic diarrhea, rheumatoid arthritis, degenerative disease of large joint, vasculitis, and the possibility of malignancy based on history and examination and Theophylline use during a month prior to the enrollment

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
HS-CRP serum levels. Timepoint: Before and after intervention. Method of measurement: ELISA.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr. Naseh Sigari

Kurdistan University of Medical Sciences

naseh46@muk.ac.ir+98 87 1328 6113

Outcome results

None listed

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