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Emergency Intestinal Anastmosis

A Comparative Study Between Stapled and Handsewn Intestinal Anastmosis in Emergency Laparotomy

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07321743
Enrollment
90
Registered
2026-01-07
Start date
2024-12-20
Completion date
2025-12-20
Last updated
2026-01-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Intestinal Anastomosis

Keywords

stapler, handsewn, anastomotic leakage, intestinal obstruction

Brief summary

The goal of this clinical trial is to compare the outcomes of emergency intestinal anastomosis after stapled and handsewn anastmosis. The main question it aims to answer are: Is stapled intestinal anastmosis is better than handsewn anastmosis in emergency laparotomy? Participants at surgical emergency unit: * Had intestinal anastmosis either by stapler or handsewn. * kept in hospital for follow up and detection of complications like wound infection and leakage. * Either discharged or managed according to the complications * Outcomes were compared between the two groups

Interventions

PROCEDUREemergency intestinal anastmosis surgery

cases with intestinal trauma, perforation or intestinal obstruction had emergency laparotomy and intestinal anastmosis was done

Sponsors

Zagazig University
Lead SponsorOTHER_GOV

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* patients admitted to emergency surgery and needed intestinal anastmosis

Exclusion criteria

* patients below 18 years old * immune-compromised patients e.g. corticosteroids therapy, autoimmue disease

Design outcomes

Primary

MeasureTime frameDescription
intestinal leakagefrom one day to two weeks after surgeryintestinal leakage output calculated in ml by weighing dressing or calculating the drain output

Secondary

MeasureTime frameDescription
operation timefrom incision time to closure (0 to 5 hours)operation time in minutes was calculated
bleedingfrom one hour to two days after surgerybleeding amount was calculated in ml
hospital stayfrom one day to one month after surgeryhospital stay was recorded in days
post-operative painfrom one to three days after after surgerypain was evaluated by the visual analogue scale from 1 to 10. score 1 means least painful, score 10 means very painful

Countries

Egypt

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026