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NCT07289568Enrolling by invitation

Surgical Outcomes in Splenic Flexure Cancers: A Multicenter Comparison of Segmental vs. Extended Hemicolectomy (SPARROW Study)

Surgical Outcomes in Splenic Flexure Cancers: A Prospective, Multicentric Observational Cohort Study Comparing Segmental Hemicolectomy and Extended Hemicolectomy - The SPARROW Study

Source: ClinicalTrials.gov · Last updated 17 Dec 2025

Brief summary (registry, in English)

SPARROW Study: Surgical Outcomes in Splenic Flexure Cancer Colonic cancers located at the splenic flexure where the transverse colon turns into the descending colon are uncommon and represent less than 10% of all colorectal cancers. Because of their unique location between the blood supply of the right and left colon, there is no clear agreement on which surgical method provides the best results. Two main procedures are used: Segmental hemicolectomy, which removes only the part of the colon containing the tumor, and Extended hemicolectomy, which removes a larger section of the colon and more lymph nodes. The SPARROW Study is a prospective, multicenter observational study designed to compare these two surgical approaches in patients with splenic flexure cancer. The study will include about 140 patients (70 in each group) from multiple tertiary colorectal centers in Turkey and Europe. Researchers will collect information about each patient's surgery, recovery, and follow-up outcomes. The main outcomes include postoperative ileus, leakage at the surgical connection (anastomosis), wound infection, and total postoperative complications. Other outcomes include number of lymph nodes removed, complete tumor resection (R0), hospital stay, recovery time, reoperation, and 3-year overall and disease-free survival. By analyzing both short- and long-term results, the SPARROW Study aims to provide high-quality evidence to guide surgeons in choosing the best and safest operation for patients with splenic flexure cancers. All participants will provide written informed consent before joining the study. The study has received ethical approval from the Koç University Ethics Committee and will be conducted in accordance with the Declaration of Helsinki.

Status (registry)
Enrolling by invitation
Study type
Observational
Enrollment
140 (estimated)
First submitted
18 Nov 2025
Start date
5 Oct 2025
Primary completion date
Oct 2028
Lead sponsor
Acibadem University
NCT number
NCT07289568

What you commit to

  • Study type: Observational
  • Planned participants: 140
  • From 5 Oct 2025 to the primary completion date, Oct 2028
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Previous colorectal resection involving the splenic flexure

Other illness

  • Emergency surgery for obstruction, perforation, or bleeding
  • Presence of synchronous colorectal malignancy or distant metastasis requiring simultaneous resection

Other

  • Non-adenocarcinoma histology (e.g., lymphoma, neuroendocrine tumor, gastrointestinal stromal tumor)
  • Patients undergoing palliative resections, local excisions, or bypass procedures without curative intent
  • Patients with incomplete clinical or pathological data or those lost to follow-up before 30 days postoperatively

Who the study is looking for

  • Adult patients aged 18 years or older
  • Histologically confirmed adenocarcinoma of the splenic flexure
  • Elective surgical resection performed with curative intent (segmental colectomy or extended hemicolectomy)
  • Availability of complete perioperative and follow-up data
  • Written informed consent provided prior to participation
  • Surgery performed by colorectal or general surgeons meeting institutional eligibility criteria (≥20 colorectal cancer cases/year, ≥2 years of colorectal training)

Age in the registry: 18 years to 80 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Acibadem University
Coordinator of this site? Confirm its status
IstanbulTurkey (Türkiye)Unknown status

This page is information, not medical advice. Discuss any trial with your doctor.