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Study identifier: NCT07615036 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

AP-NOSES: A Prospective Multicentre Registry of Natural Orifice Specimen Extraction in Minimally Invasive Colorectal Surgery

Condition: Colorectal Neoplasms · Incisional Hernia  ·  Sponsor: Singapore General Hospital

PhaseN/A
Planned participants800
Who can joinAll sexes, 21 Years to no upper limit
Healthy volunteersNo

About this study

Natural orifice specimen extraction (NOSE) is a minimally invasive colorectal surgical technique in which the surgical specimen is removed through a natural orifice, including transanal or transvaginal routes, thereby avoiding an abdominal extraction incision. Observational studies suggest that NOSE may reduce wound-related morbidity and improve postoperative recovery, but prospective multicenter data evaluating long-term outcomes remain limited. AP-NOSES is a prospective, multicenter observational registry evaluating clinical, patient-reported, and long-term wound outcomes following minimally invasive colorectal surgery with NOSE or transabdominal specimen extraction. The primary objective is to compare time to incisional hernia within 24 months between NOSE-eligible patients undergoing planned NOSE extraction and NOSE-eligible patients undergoing planned transabdominal extraction. Secondary objectives include evaluation of postoperative complications, extraction-related morbidity, bowel function, urinary and sexual function, oncologic outcomes, and long-term patient-reported and clinical outcomes across participating centers. This study does not alter routine clinical care. Surgical technique, perioperative management, and follow-up are performed according to local institutional practice.

This description comes directly from the study's public registry record.

Talk to the study team

Isaac Seow-En, MBBS, FRCSEd  ·  +6563213853  ·  isaac.seow.en@singhealth.com.sg

Always discuss trial participation with your own doctor first.

Locations (1)

Singapore General HospitalSingapore, SingaporeRecruiting

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Source record: clinicaltrials.gov/study/NCT07615036