Skip to content

Three-port versus four-port laparoscopic cholecystectomy

Randomized clinical trial of 3-port versus conventional 4-port laparoscopic cholecystectomy for cholelithasis treatment

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT201202098375N5
Enrollment
60
Registered
2014-01-28
Start date
2013-11-22
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

Laprascopic cholecystectomy. Calculus of gallbladder with acute cholecystitis

Interventions

Intervention 1: Interventional group: three-port laparoscopic cholecystectomy. Intervention 2: Control group: four-port laparoscopic cholecystectomy.
Treatment - Surgery
Interventional group: three-port laparoscopic cholecystectomy
Control group: four-port laparoscopic cholecystectomy

Sponsors

Vice-Chancellor for Research, Birjand University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
35 Years to 50 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: consent to participate in the study; acute cholecystitis; BMI less 35; the absence of severe inflammation of gallbladder;absence of cardiovascular disease; age less 50 years Exclusion criteria: lack of consent to participate in the study; severe inflammation in gallbladder and gangrenous cholecystitis; BMI more 35; cardiovascular disease; age more 50 years; need to use the fourth port; longer operation time more than the average total operation time; need to put the drain

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Post laparoscopic pain. Timepoint: 4 hours after operation. Method of measurement: Post laparoscopic pain will be evaluated by a researcher who does not know the kind of operation with VAS ( Visual Analogous Scale). In this scale, each patient evaluates his/her pain from 0 to 10.

Secondary

MeasureTime frame
Level of patient's satisfaction. Timepoint: 4 hours after operation. Method of measurement: Based on patient self-report.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr Ghodrat Allah Naseh

Surgery Ward, Emam Reza Educational Hospital, Birjand University of Medical Sciences

Nasehghodrat@yahoo.com+98 56 1222 2300

Outcome results

None listed

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