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Not yet recruitingNCT06031311Updated Sep 14, 2023

Pulmonaryhypertension in Copd at Different Levels of Smoking

An observational study in Pulmonary Hypertension, sponsored by Assiut University. Not yet recruiting. Open to participants aged 18 Years to 100 Years. Per ClinicalTrials.gov, last updated 2023-09-14.

Sponsored by Assiut University · Observational

From the registry’s dates

  • Primary completion was expected by Oct 2024, 2 years ago, but the record still lists the study as not yet recruiting.
Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
138
Ages
18 Years to 100 Years
Sex
All
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Study summary

To identify Predictors of pulmonary hypertension in COPD patients and its relation to different levels of smoking

Read the detailed description

COPD is a heterogeneous lung condition characterized by chronic respiratory symptoms (dyspnea, cough, expectoration and/or exacerbations) due to abnormalities of the airways (bronchitis, bronchiolitis) and/or alveoli (emphysema) that cause persistent, often progressive, airflow obstruction.It is also the most common cause of deaths in patients with chronic respiratory disease, the fatality rate in USA is 0.41%.Pulmonary Hypertension is the most common serious complication in COPD patients ; which occurs in up to 30% of patients and increases the mortality rate.Smoking is the leading cause of chronic obstructive pulmonary disease (COPD) Smoking is also a trigger for COPD flare-ups.Smoking damages the air sacs, airways, and the lining of your lungs. Injured lungs have trouble moving enough air in and out, so it's hard to breathe

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Conditions studied

  • Pulmonary Hypertension
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In context

Hypertension, Pulmonary

1,105 studies on the registry are indexed under Hypertension, Pulmonary; 234 are open to participants now.

This study's planned enrollment of 138 is above the median of 116 across 386 observational studies indexed under Hypertension, Pulmonary.

Browse Hypertension, Pulmonary studies →

Lead sponsor

Assiut University is the lead sponsor of 4,901 studies on the registry; 2,098 are open to participants now.

Of its 13 completed or terminated interventional studies of FDA-regulated products, 0 (0%) have results posted.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
18 Years to 100 Years
Sexes eligible
All
Sampling method
Non-probability sample

Study population

Full clinical history including:[demographic data and clinical symptoms including cough with expectoration ,dyspnea,chest wheeze,...etc] 2.Full clinical examination. 3.laboratory investigations: Complete blood picture , kidney function test, liver function test,coagulation profile 4.Arterial blood gases [Pao2, Paco2,Sao2,Hco3, P(A_a)o2 ] 5.PFTS:will be performed and classified into: Post bronchodilator FEV1/FVC \<0.7

GOLD 1 - mild: FEV1 ≥80% predicted. GOLD 2 - moderate: 50% ≤ FEV1 \<80% predicted. GOLD 3 - severe: 30% ≤ FEV1 \<50% predicted. GOLD 4 - very severe: FEV1 \<30% predicted [5] 6.Echocardiography:is non invasive and easily accessible tool in the diagnosis of any patient with suspected PH. ePASP is estimated by calculating Doppler estimated trans tricuspid gradient (TR gradient= 4 x (TR velocity)2) and adding estimated right atrial pressure to it based on the size of the inferior vena cava and collapsibility.[6]

Inclusion criteria

  • 1.All patients admitted to chest department or presented to our outpatient clinic with clinical and functional diagnosis of COPD among both sexes will be included 2.Age >18 years Old

Exclusion criteria

Exclusion Criteria:

  • 1.Patients under 18 years old. 2.pregnant patients. 3.patients with history hypertension or valvular diseases 4.Cardiomyopathic patient 5.Patients with concomitant obstructive sleep apnea 6.Patients with collagen vascular disease 7.Patients with thrombo-embolic disease 8. Patients with any chronic chest disease other than COPD
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Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
138 participants (estimated)
Patient registry
No

Interventions

  • Diagnostic testEchocardiography and HRCT

    Echocardiography:is non invasive and easily accessible tool in the diagnosis of any patient with suspected PH.HRCT: is a non-invasive and easily accessible tool to detect pulmonary hypertension in COPD patients.

06

What researchers measure

Primary outcomes

  1. Predictors of pulmonary hypertension in COPD patients

    Predict pulmonary hypertension in COPD patients

    Time frame: 1 year

Secondary outcomes

  1. Relationship between different levels of smoking and predictors of degree of pulmonary hypertension

    Levels of smoking (mild.moderate.sever.non smoker) and it's relation to pulmonary hypertension in COPD patients

    Time frame: 1 year

07

Study locations

No study locations are listed for this record.

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References and documents

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Sep 14, 2023, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT06031311
Lead sponsor
Assiut University
Responsible party
Shrouk Mohamed Salah Mosleh (Resident doctor, Assiut University) — Principal investigator
First posted
Sep 11, 2023
Start date
Oct 1, 2023 (estimated)
Primary completion
Oct 1, 2024 (estimated)
Completion
Dec 1, 2024 (estimated)
Last update
Sep 14, 2023

Study contacts

Shrouk Mohamed Salah, Resident physician
Contact
Shrouksalah806@gmail.com
01150637673
Marwan Nasr Sleem, Lecturer of Chest diseases and
Contact
faridamarwan2014@yahoo.com
01150637673

Oversight

FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is not yet recruiting, as verified in Sep 2023. You cannot join it, but the record below documents what was studied.

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