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Effect of Nicotine and Consulting on smoking cessation and pulmonary indexes in patients candidate for heart surgery

Comparison of Nicotine Replacement Therapy (NRT) and Nursing consulting on smoking cessation and Spiro metric indexes of smokers candidate for Coronary Artery Bypass Graft (CABG)

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2014071518499N1
Enrollment
60
Registered
2014-10-06
Start date
2014-08-06
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

Smokers Candidate for Coronary artery Bypass Graft surgery (CABG). Atherosclerotic heart disease

Interventions

Intervention 1: In NRT group, at the beginning of participation, researcher will explain instructions and dosage of using nicotine gums for patients and their family. Then we will give patients two bo
Treatment - Drugs
Behavior
In NRT group, at the beginning of participation, researcher will explain instructions and dosage of using nicotine gums for patients and their family. Then we will give patients two boxes of gums till
In consulting group, intervention will be accomplished by phone-consulting (in 10-15 minutes duration each time) and 3 times a week, in non-hospitalization days. (For hospitalization days consults wil

Sponsors

Tehran University of Medical sciences Vice chancellor for research
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: Inclusion Criteria: 1. Age 18 years or more 2. Patients tend to have quit smoking 3. Candidates of CABG surgery 4. Non-emergency CABG surgery 5. Smoking addiction 6. No history of mental disorder or having psychologically Cooperation 7. Not allergic to nicotine patches and gum 8. Ability to properly use of nicotine patches 9. Non-use of other cessation forms 10. Have no Addiction to alcohol and other drugs 11. Not having acute or severe respiratory disorders Exclusion Criteria: 1. Occurrence of unstable medical conditions and inability to continue cooperation in the study. 2. Refuse cooperation in study or continue smoking during the study period 3. Conflict to other postoperative complications in such a way that makes it impossible to continue study participation

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Smoking Cessations. Timepoint: Measurements time intervals: Smoking cessation: It will be monitored according to time table. In the way that, during 3 weeks before and till 3 weeks after surgery which is research time table, we will contact to patients and their families separately 2-3 times a week for examining adherence to cessations. Method of measurement: For smoking cessation: telephone contacts to patients and their families according to time table.;Patients' Spirometric Indexes. Timepoint: Spirometric indexes: examinations of patients' pulmonary indexes and function by computerized spirometry test in two times (one day before surgery and 2 weeks after that). Method of measurement: For spirometric indexes: by spirometry Device.

Secondary

MeasureTime frame
Demographic data and medical history. Timepoint: at the beginning of study in physician clinic. Method of measurement: by interviewing and questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactFateme Bakhshi

Tehran University of medical Sciences- School of Nursing and Midwifery

f_bakhshi@razi.tums.ac.ir+98 35 1620 4053

Outcome results

None listed

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