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Study the difference in the biopsy quality between right and left lobe of liver using endoscopic ultrasound

RIGHT LOBE VERSUS LEFT LOBE LIVER BIOPSY UNDER ENDOSCOPIC ULTRASOUND GUIDANCE: A PROSPECTIVE COMPARATIVE STUDY

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2023/06/053505
Enrollment
28
Registered
2023-06-02
Start date
Unknown
Completion date
Unknown
Last updated
2023-08-21

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

Conditions

Health Condition 1: K746- Other and unspecified cirrhosis ofliver

Interventions

Intervention1: Right lobe liver biopsy: EUS-LB of right lobe using wet suction technique as mentioned below: i. Patients undergoing EUS-LB will receive moderate sedation using midazolam or nalbuphine

Sponsors

Jayanta Samanta
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Patients requiring liver biopsy 2. Informed consent obtained from the patient 3. Patients >18 years old

Exclusion criteria

Exclusion criteria: 1. Unable to obtain informed consent from the patient 2. Medically unfit for sedation 3. Pregnant patient 4. Presence of a mass lesion in the liver requiring biopsy visualized on cross-sectional imaging 5. Irreversible coagulopathy as determined by platelet count 1.5 6. Unable to stop anticoagulation or anti-platelet therapy for 5 days prior to the procedure 7. Hemophilia 8. Presence of an alternative etiology for elevated liver tests seen during liver biopsy, e.g. biliary obstruction during EUS examination 9. Suspected or proven malignant liver disease. 10. severe cardiovascular and pulmonary diseases

Design outcomes

Primary

MeasureTime frame
Number of complete portal tracts (CPT)Timepoint: At procedure.

Secondary

MeasureTime frame
1. Post processing maximum (or aggregate) specimen length 2. Length of the longest specimen 3. Adequacy of tissue sample 4. Rates of specimen adequacy (whether pathological diagnosis is reached or not) Timepoint: At procedure;5. Assessment of pain scores (subjective & objective) 6. Pain medication requirement: use of narcotics/analgesics in both arms, post-procedure Timepoint: Immediate post procedure, 1 hr., 12 hr., 24 Hr.;7. Rate of adverse eventsTimepoint: Immediate post procedure, 24 hr, 1 week

Countries

India

Contacts

Public ContactJayanta Samanta

Post Graduate Institute of Medical Education and Research, Chandigarh

dj_samanta@yahoo.co.in9855319529

Outcome results

None listed

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