Skip to content

Comparing efficacy of Ultrasonography Guidance versus Computed Tomography Guidance for Peripheral Lung Lesion Biopsies

A Comparative Analysis of performance parameters of Ultrasonography Guidance versus Computed Tomography Guidance for Peripheral Lung Lesion Biopsies

Status
Recruiting
Phases
Phase 2Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2023/01/048763
Enrollment
114
Registered
2023-01-05
Start date
Unknown
Completion date
Unknown
Last updated
2023-02-06

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

Conditions

Health Condition 1: 8- Other Procedures

Interventions

Intervention1: USG Guided biopsy lung biopsy: Real time based USG Guided trans-thoracic biopsy of peripheral lung lesion will be done with help of co-axial biopsy needle. Intervention2: Trans-thoracic

Sponsors

AIIMS Patna
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Intrathoracic peripheral lung lesions of size more than 1cm and abutting the pleura. 2. Peripheral lung lesion not lying in close proximity of major organ or blood vessels based of CT /MRI Chest. 3. Lung lesion visible on Ultrasongraphy. 4. Age > 18 years of age. 5. Patients giving informed consent

Exclusion criteria

Exclusion criteria: 1. Central lung lesions not abutting pleura or ground-glass lesions. 2. Lesion lying in close proximity to major blood vessel or major organ. 3. Lesion not visible on Ultrasonography (Emphysematous overlying lung, located behind rib or scapula) 4. Age 5. Patients not giving informed consent. 6. Patients with Thrombocytopenia. 7. Patients with deranged coagulation profile.

Design outcomes

Primary

MeasureTime frame
To evaluate the efficacy of US guided biopsy of peripheral lung lesion with CT guided biopsy.Timepoint: Outcome will be assessed at end of study

Secondary

MeasureTime frame
1. To compare the safety or complications of Ultrasonography guided biopsy of peripheral lung lesion to CT guided. 2. To assess suitability in debilitated and uncooperative patients.Timepoint: Outcome will be assessed at end of study and efficacy of both procedures would be compared

Countries

India

Contacts

Public ContactDr Rajesh kumar Yadav

All India Institute of Medical Sciences, Patna

drsaurabhkarmakar@gmail.com9839443375

Outcome results

None listed

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