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Comparison of Fast track with routine regimen in reducting postoperative thoracotomy pain and respiratory complications

Comparison of Fast track with routine regimen in reducting postoperative thoracotomy pain and respiratory complications

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
IRCT
Registry ID
IRCT138902093831N1
Enrollment
56
Registered
2010-10-09
Start date
2010-04-21
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

Benign and Malignant disease of the lung, reduction of operative complications with regional anesthesia.

Interventions

Intervention 1: Bupivacaine 0.25% + Fentanil (1mg per hour) for 3 days after thoracotomy via epidural catheter. Intervention 2: Morphine (1mg per hour intravenous + Intercostal block with marcaine 0
Treatment - Drugs
Morphine (1mg per hour intravenous + Intercostal block with marcaine 0.25% for 3 days
Bupivacaine 0.25% + Fentanil (1mg per hour) for 3 days after thoracotomy via epidural catheter

Sponsors

Tabriz University Of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: Both genders of patients with pulmonary disease which treated with elective thoracotomy, absence of blood coagulopathy, class I, II, or III American society of Anesthesiology, no underlying disease (pneumonia, Bronchitis, Asthma) Exclusion criteria: class IV, V ASA, FE less than 40%, patients with Aortic stenosis, intraoperative bleeding more than 25% that needed blood transfusion, Time of Surgery more than three hours

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Post-thoracotomy pain. Timepoint: Daily until one week after surgery. Method of measurement: Respiratory postoperative pain and clinical symptom and signs (Pain seeing measurement).;ICU needed. Timepoint: Daily until one week after surgery. Method of measurement: Respiratory postoperative pain and clinical symptom.;Mechanical ventilation needed. Timepoint: Daily until one week after surgery. Method of measurement: Respiratory postoperative pain and clinical symptom.;Respiratory complications. Timepoint: Daily until one week after surgery. Method of measurement: Respiratory postoperative pain and clinical symptom.

Secondary

MeasureTime frame
Mortality. Timepoint: Daily until one week. Method of measurement: Death rate.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMohsen Sokouti

Cardiothoracic Surgery Department

Sokoutim@tbzmed.ac.irBabak756a@yahoo.com+98 41 1336 6634

Outcome results

None listed

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