Comparing two surgical techniques for rectal cancer treatment
End to End Versus Side to End Anastomosis After Anterior Resection of Cancer Rectum
This study is testing which surgical method for rectal cancer works better for patients by looking at how it affects their bowel function and recovery.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 20 (estimated) |
| Ages | 18 Years to 80 Years |
| Sex | All |
| Sponsor | Sohag University Academic / other |
| Locations | 1 site (Sohag) |
| Trial ID | NCT06311279 on ClinicalTrials.gov |
What this trial studies
This study compares the outcomes of end to end versus side to end anastomosis following anterior resection of rectal cancer. It focuses on bowel functional outcomes, including stool frequency, urgency, incomplete defecation, and incontinence, as well as surgical outcomes such as operative time, postoperative complications, and hospital stay. The goal is to improve the quality of life for patients undergoing surgery for rectal cancer by evaluating which technique yields better functional results. The study involves patients aged 18 to 80 who are undergoing laparoscopic or open surgery for rectal cancer.
Who should consider this trial
Good fit: Ideal candidates are adults aged 18 to 80 undergoing laparoscopic or open anterior resection for rectal cancer.
Not a fit: Patients with synchronous colorectal carcinoma, those requiring emergency surgery, or those with a history of segmental resections may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could lead to improved bowel function and quality of life for patients undergoing surgery for rectal cancer.
How similar studies have performed: Other studies have shown varying success with similar surgical techniques, but this specific comparison is less commonly tested.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * 18 years of age to 80 years. * Laparoscopic or open anterior resection of cancer rectum. Exclusion Criteria: * synchronous colorectal carcinoma * emergency surgery * history of colon or rectal segmental resections * fixed rectal carcinoma who received preoperative radiotherapy
Where this trial is running
Sohag
- Sohag university — Sohag, Egypt (Recruiting)
Study contacts
- Principal investigator: Nabil A Al-Ameer, MD — Sohag University
- Study coordinator: Nabil A Al-Ameer, MD
- Email: Nabil.abdelnaser@med.sohag.edu.eg
- Phone: 1118416290
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.