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Comparison of health status outcome in people undergoing lung surgery using special tube used for aerating one lung under two different types of anesthesia drugs.

A comparative study of quality of life using EQ-5D-3L questionnaire between patients undergoing lung resection with one-lung ventilation under isoflurane or propofol anesthesia- A randomized controlled trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2023/06/054240
Enrollment
80
Registered
2023-06-21
Start date
Unknown
Completion date
Unknown
Last updated
2023-06-26

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: O- Medical and Surgical

Interventions

Intervention1: Inhalational anesthesia during one lung ventilation: During the whole surgical duration anesthesia will be maintained using inhalational agent (Isoflurane) Control Intervention1: Intrav

Sponsors

Jawaharlal Institute of Postgraduate Medical Education and Research
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Adults aged 20-65 years ASA-PS I-III Patients undergoing elective thoracotomy for lung resection with OLV

Exclusion criteria

Exclusion criteria: Patients with severe cardiac disease, hepatic or renal dysfunction patients with a prior allergic history of any study drug Patients taking sedative, opioid or sleep aid drugs Patients with Psychiatric or neurological disorder BMI >30 kg/m2 Pregnancy History of pneumonectomy or lung volume reduction surgery patients with severe systemic infections

Design outcomes

Primary

MeasureTime frame
To compare EQ5D3L scores 3 months after surgery in patients undergoing lung resection under one lung ventilation between patients administered inhalation & intravenous anesthesiaTimepoint: Outcome will be analysed after collection of data for the requisite sample size

Secondary

MeasureTime frame
1. To compare the composite of Neurological, Cardiovascular & Pulmonary complications 2. To compare the length of hospital stay 3. To compare the need of mechanical Ventilation support required postoperatively 4. To compare the number and types of rescue strategy adopted intraoperatively: PEEP/CPAP/High FiO2/Inotropes support/ Crossover to other strategyTimepoint: Outcome will be analysed after collection of data for the requisite sample size

Countries

India

Contacts

Public ContactNirusha Regmi

Jawaharlal Institute of Postgraduate Medical Education and Research

jipmersatyen@gmail.com7708746042

Outcome results

None listed

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