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Clinical Trials/NCT05565508
NCT05565508
Completed
Not Applicable

a Prospective Randomized Controlled Trial Evaluating Safe Laparoscopic Access in Patients With Previous Abdominal and Pelvic Surgery

Zagazig University1 site in 1 country172 target enrollmentMarch 20, 2020

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Laparoscopic Surgery
Sponsor
Zagazig University
Enrollment
172
Locations
1
Primary Endpoint
time needed to access the peritoneal cavity
Status
Completed
Last Updated
3 years ago

Overview

Brief Summary

the study discussed the safety of new technique for primary port insertion in cases of previous abdominal and pelvic surgery

Detailed Description

the study discussed the safety of new technique for primary port insertion in cases of previous abdominal and pelvic surgery and comparing the new technique group (A) patients to already known technique called (Hasson's technique) group (B) patients

Registry
clinicaltrials.gov
Start Date
March 20, 2020
End Date
July 20, 2022
Last Updated
3 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Mohamed lotfy

prof. Dr

Zagazig University

Eligibility Criteria

Inclusion Criteria

  • Patients more than 18 year-old with history of previous abdominal and/or pelvic surgery.
  • underwent laparoscopic surgery in general surgery departments in both centers from March, 2020 to july, 2022.

Exclusion Criteria

  • Patients with distended abdomen due to bowel obstruction.
  • Patients with uncorrected coagulopathy.

Outcomes

Primary Outcomes

time needed to access the peritoneal cavity

Time Frame: the first 15 minutes of operation

time needed to access the peritoneal cavity

numbers of trials till the good peritoneal access achieved

Time Frame: the first 15 minutes of operation

numbers of trials till the good peritoneal access achieved

Secondary Outcomes

  • rate of complications(the first 15 minutes of operation)

Study Sites (1)

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