cholecystitis. ??? ??????? ???? ???? (??? ?? ????)
Conditions
Interventions
Intervention 1: Control group(4 port): In this group, 4 laparoscopic port are used for cholesystemy. 10-mm port in the umblicus, 5 mm port in epigastric area (sub-xiphoid), 5 mm port in midclavicular
Treatment - Surgery
Control group(4 port): In this group, 4 laparoscopic port are used for cholesystemy. 10-mm port in the umblicus, 5 mm port in epigastric area (sub-xiphoid), 5 mm port in midclavicular line about 2 cm
Intervention group 1 (3 port cholecystectomy): In this group one 10-mm port in inserted from the umblical area and two 5 mm ports are inserted in epigastric area (sub-xiphoid) and right midclavicular
Intervention group 2 (Single incision laparoscopic cholecystectomy): In this group a 2 cm vertical incision is made in the umblicus and all three ports (one 10-mm and two 5-mm ports) are inserted from
Sponsors
Tehran University of Medical Sciences
Eligibility
Sex/Gender
All
Age
18 Years to 80 Years
Inclusion criteria
Inclusion criteria: Inclusion criteria: Indication for laparoscopic cholecystectomy, Informed consent for participating in the study Exclusion Criteria: Severe inflammation of gallbladder, Bile duct stone needing bile exploration, Drug addiction, planned surgery not progressed
Exclusion criteria
Exclusion criteria:
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Postoperative narcotic usage. Timepoint: Continousely recorded and measured at the time of discharge. Method of measurement: Patient controlled analgesia device. | — |
Secondary
| Measure | Time frame |
|---|---|
| Postoperative nausea and vomiting. Timepoint: 12 hours intervals till discharge. Method of measurement: History taking.;Wound infection. Timepoint: At the time of discharge and 7 days later. Method of measurement: Physical examination.;Intraoperative adverse events. Timepoint: At the end of surgery. Method of measurement: Questionnaire for the surgeon.;Surgeon opinion about surgery difficulty. Timepoint: At the end of surgery. Method of measurement: Questionn to the surgeon with likert scale.;Post operathve Hospital stay. Timepoint: At the time of discharge. Method of measurement: based on medical reocords.;Patient's satisfaction about cosmetic outcome. Timepoint: 3 months after surgery. Method of measurement: Question with likert scale.;Other systematic postoperative complication. Timepoint: At the time of discharge and 30 days later. Method of measurement: History taking and clinical records.;Postoperative pain. Timepoint: 6 hours intervals for 24 hours. Method of measurement: Visual analogue scale.;Surgery duration. Timepoint: At the end of surgery. Method of measurement: Stopwatch.;Bile leakage or bile duct trauma. Timepoint: At the time of discharge and 30 days later. Method of measurement: Clinical records. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactZhamak Khorgami
Tehran University of Medical Sciences - Shariati Hospital
Outcome results
None listed