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OncoMatch/Clinical Trials/NCT07371273

Comparative Study on the Short- and Long-term Efficacy of Q-ISR, Traditional Sub-ISR, and t-ISR

Is NCT07371273 recruiting? Yes, currently enrolling (Jun 2026). This Phase 2 trial studies non-drug interventions for colorectal cancer.

Phase 2RecruitingFudan UniversityNCT07371273Data as of Jun 2026Location: China

This comparative study evaluates the short- and long-term outcomes of Quadrant-based Intersphincteric Resection (Q-ISR) versus traditional subtotal ISR (Sub-ISR) and conventional/total ISR (t-ISR) in patients with ultra-low rectal cancer undergoing sphincter-preserving surgery, with short-term endpoints focusing on perioperative safety (operative time, blood loss, length of stay, and postoperative complications such as Clavien-Dindo grade ≥II, anastomotic leakage/stricture, and stoma reversal) and long-term endpoints assessing anorectal function recovery (LARS and Wexner scores after stoma closure) and oncologic efficacy (R0 resection, recurrence patterns, and survival outcomes), aiming to determine whether a quadrant-tailored resection strategy can better balance tumor control with anal function preservation.

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Extracted eligibility criteria

Cancer type

Colorectal Cancer

Disease stage

Excluded: Stage DISTANT METASTASIS

Presence of distant metastasis [excluded].

Performance status

ASA 0–3

Demographics

Ages ≤ 75

Structured fields extracted by AI. May contain errors — verify against the official protocol.

Frequently asked questions

Is NCT07371273 currently recruiting?

Yes, this trial is currently recruiting patients.

Is there an age limit?

Yes. Patients must be 75 years or younger.

Could you qualify for this trial?

Enter your biomarker results to see how this trial's eligibility criteria match your specific cancer profile.

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