End to End Anastomosis With Omega Suture Versus End to Anterior Rectal Wall In Colorectal Anastomosis in Sigmoid and Upper Rectal Cancer

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorAin Shams University

About this trial

The aim of this study is to compare end to end anastomosis with omega suture versus end to anterior rectal wall in colorectal anastomosis as regard post operative anastomotic leakage, bowel function, operative time and intra operative blood loss.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Patients aged >18 years.

Both sexes.

Recto sigmoidal carcinoma.

Upper rectal cancer.

Disqualifiers

Patients younger than 18 years

Recurrent or non-resectable cancer

Complicated cancer (e.g., obstructed or perforated)

Previous left-sided colorectal surgery or anorectal surgeries

Trial design

Design model

Parallel

Treatments tested in this trial

  • End to end with Omega suture

    Other intervention

    After the rectum was divided with a linear stapler, the circular stapler was placed allowing the anvil rod to penetrate the rectal stump near the linear stapler line. An omega suture including both ends of the linear stapler line was placed. The linear stapler line was approximated around the anvil rod of the circular stapler in an omega shape fashion as the omega suture was tied. This technique resulted in a complete resection of linear stapler line by the circular stapler.

  • End to anterior rectal wall

    Other intervention

    A burse string suture was applied over the anvil of the circular stapler at the transection point of the descending colon using prolene 2/0. The circular stapler introduced though the anus and its rod directed toward the anterior rectal wall and colorectal anastomosis was performed.

Treatment groups

40 Participants
are divided into 2 treatment groups
Group A: Group A(end to end with Omega suture)Other 1 intervention
Group B: Group B (end to anterior rectal wall)Other 1 intervention

Trial outcomes

Primary outcomes

1

Anastomotic leakage

Anastomotic leakage will be measured for 5 days after surgery

Time frame
5 days after surgery

Secondary outcomes

1

Operative time

Operative time will be measured from the start of surgery till the end of surgery.

Time frame
Until the procedure is completed
2

Hospital stay

Hospital stay will be assessed from admission till discharge from hospital

Time frame
28 days postoperative
3

Time of bowel function

Time of bowel function will be assessed

Time frame
7 days postoperative
4

Wound complications

Wound complications will be recorded as bleeding and infection.

Time frame
7 days postoperative

Other outcomes

Sponsors and contacts

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