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Randomised clinical trial of longitudinal versus torsional mode ultrasound in laparoscopic cholecystectomy

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN87527062
Enrollment
160
Registered
2003-09-12
Start date
2003-01-01
Completion date
Unknown
Last updated
2015-01-13

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

Conditions

Surgery: Laparoscopy Surgery Laparoscopy

Interventions

Randomised controlled trial. Random allocation to: A. Longitudinal Mode Ultrasound B. Torsional Mode Ultrasound

Sponsors

Record provided by the NHS Trusts Clinical Trials Register - Department of Health (UK)
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Patients undergoing laparoscopic cholecystectomy.

Exclusion criteria

Exclusion criteria: Added as of 29/04/2008: 1. Oral anticoagulant treatment 2. Known coagulation disorder 3. American Society of Anaesthesiologists (ASA) grade 3 or more 4. Aged less than 16 years 5. Pregnancy 6. Mental illness 7. The need to explore the common bile duct at the time of surgery

Design outcomes

Primary

MeasureTime frame
Current primary outcomes as of 29/04/2008: Operative blood loss, calculated within 24 hours post surgery. Previous primary outcomes: Operating time, blood loss, post operative complications.

Secondary

MeasureTime frame
Added as of 29/04/2008: 1. Gallbladder dissection time, measured during laparoscopic cholecystectomy 2. Gallbladder perforation rate, measured during laparoscopic cholecystectomy 3. Need for monopolar electrocoagulation, measured during laparoscopic cholecystectomy 4. Complications, recorded post-operatively

Countries

United Kingdom

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Apr 3, 2026