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Trial Title:
Short Term Surgical Outcomes of Anatomical Versus Non Anatomical Laparoscopic Liver Resection for Liver Tumors
NCT ID:
NCT06271109
Condition:
Liver Neoplasms
Conditions: Official terms:
Liver Neoplasms
Liver Extracts
Study type:
Observational [Patient Registry]
Overall status:
Enrolling by invitation
Study design:
Time perspective:
Other
Intervention:
Intervention type:
Procedure
Intervention name:
Anatomical laparoscopic liver resection for liver neoplasms
Description:
resection of liver tumors laparoscopically based on surgical anatomical segmentation of
the liver
Arm group label:
laparoscopic Anatomical liver resection
Intervention type:
Procedure
Intervention name:
Non-Anatomical laparoscopic liver resection for liver neoplasms
Description:
resection of liver tumors laparoscopically not based on surgical anatomical segmentation
of the liver
Arm group label:
laparoscopic Non Anatomical liver resection
Summary:
aimed to discuss the short term surgical outcomes of Anatomical versus Non anatomical
laparoscopic Liver resection for Liver tumors.
Detailed description:
This study aimed to be both prospective and retrospective study including the cases of
laparoscopic liver resection that was done and will be done during the period from
December 2021 to June 2025. This study will include cohort of patients who met the
eligible criteria.
Complete history taking with special concern to the following:
- Age, sex and life style.
- present medical history: hepatic condition and other debilitating diseases.
- Past medical History: blood transfusion, hepatitis, liver cirrhosis and history of
hospital admission.
Complete local examination of the abdomen including:
- Local examination of the skin overlying for any signs of infection, radiation
fibrosis and or presence of sinuses
- Percussion for presence of ascites
- Palpation for cirrhosis or any palpable masses investigations will be carried
1. Ultrasonography: routine abdominal US for every case.
2. Triphasic CT scan
3. CT volumetric study to evaluate remaining liver volume when needed.
4. Dynamic or triphasic MRI if needed
5. Metastatic work up (CT chest, bone scan and PET scan in selected patients).
6. Preoperative histopathological examination when needed.
7. routine laboratory investigations
Criteria for eligibility:
Study pop:
patient with liver neoplasms candidate for resection and fit for surgery
Sampling method:
Probability Sample
Criteria:
Inclusion Criteria:
- all patients diagnosed with liver tumors (benign and malignant) lesions suitable for
laparoscopic liver resection (Anatomical and Non anatomical)
- Patients with Child Pugh A and early B
- Patients Fit for surgery as regard anesthesia
- Patients who accept to participate in the study and sign an informed consent
Exclusion Criteria:
- Patients with Child Pugh late B&C liver disease.
- For Patients with hepatocellular carcinoma BCLC stage C&D (extra hepatic spread and
macro vascular invasion)
- Patients with contraindications to laparoscopic surgery and (or) unfit for surgery.
Gender:
All
Minimum age:
N/A
Maximum age:
N/A
Healthy volunteers:
No
Locations:
Facility:
Name:
Sohag University
Address:
City:
Sohag
Country:
Egypt
Start date:
December 1, 2021
Completion date:
June 1, 2025
Lead sponsor:
Agency:
Sohag University
Agency class:
Other
Source:
Sohag University
Record processing date:
ClinicalTrials.gov processed this data on November 12, 2024
Source: ClinicalTrials.gov page:
https://clinicaltrials.gov/ct2/show/NCT06271109
