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Effect of oral Theophylline on chronic obstructive pulmonary disease

Comparison of oral Theophylline with Atorvastatin in reduction of serum CRP levels in patients with chronic obstructive pulmonary disease

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT2014102919747N1
Enrollment
100
Registered
2014-11-24
Start date
2014-10-19
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 obstructive pulmonary disease, unspecified

Interventions

Intervention 1: Theophylline group: tablet theophylline 200 mg(made in Dr Abidi company) every 12 hours for 2 weeks. Intervention 2: Atorvastatin group: tablet atorvastatin 10 mg( made in Dr Abidi com
Treatment - Drugs
Placebo
Theophylline group: tablet theophylline 200 mg(made in Dr Abidi company) every 12 hours for 2 weeks
Atorvastatin group: tablet atorvastatin 10 mg( made in Dr Abidi company) every 12 hours for 2 weeks
Placebo group: tablet placebo 200 mg every 12 hours for 2 weeks

Sponsors

Vice Chancellor for research of Ardebil University of Medical Science
Lead Sponsor

Eligibility

Sex/Gender
All
Age
40 Years to 70 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria:Having age between 40 to 70 years old? Having no other background diseases that change the level of CRP like infectious? rheumatologic? malignancy diseases? Lack of consumption of other drugs? Satisfaction for taking part in study. Exclusion criteria: Observation of side effect of drugs during the study? Dissatisfaction of patients in every stage of study? Consumption of other drugs at the same time.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
CRP. Timepoint: before intervention and two weeks after intervention. Method of measurement: Latex Agglutinasition test.

Secondary

MeasureTime frame
CAT score. Timepoint: before intervention and two weeks after intervention. Method of measurement: CAT test.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactSiamak Lotfi

Ardebil University of Medical Science

s_siamak_lotfi@yahoo.com+98 45 3351 8663

Outcome results

None listed

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