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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05565508
Other study ID # zuh248
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date March 20, 2020
Est. completion date July 20, 2022

Study information

Verified date October 2022
Source Zagazig University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

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


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


Recruitment information / eligibility

Status Completed
Enrollment 172
Est. completion date July 20, 2022
Est. primary completion date July 17, 2022
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 65 Years
Eligibility 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.

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
new laparoscopic access technique for group a
new laparoscopic access technique through the epigastric region
Hasson's technique for laparoscopic access in group b
Hasson's technique for laparoscopic access in group b

Locations

Country Name City State
Egypt Zagazig University Zagazig

Sponsors (1)

Lead Sponsor Collaborator
Zagazig University

Country where clinical trial is conducted

Egypt, 

Outcome

Type Measure Description Time frame Safety issue
Primary time needed to access the peritoneal cavity time needed to access the peritoneal cavity the first 15 minutes of operation
Primary numbers of trials till the good peritoneal access achieved numbers of trials till the good peritoneal access achieved the first 15 minutes of operation
Secondary rate of complications rate of complications the first 15 minutes of operation
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