ClinicalTrials.Veeva

Menu

Assessment of Autologous Blood Marker Localization in Laparoscopic Colorectal Cancer Surgery (ABILITY)

T

Tongji University

Status

Enrolling

Conditions

Colorectal Cancer

Treatments

Procedure: Laparoscopic colorectal cancer resection

Study type

Interventional

Funder types

Other

Identifiers

NCT05597384
Shanghaieasthospital-2022113

Details and patient eligibility

About

Laparoscopic colorectal surgery has been proved to have similar oncological outcomes with open surgery. Due to the lack of tactile perception, surgeons may have misjudgments in laparoscopic colorectal surgery. Therefore, the accurate localization of a tumor before surgery is important, especially in the early stages of cancer. Recently, some retrospective studies reported the use of patients' autologous blood for preoperative colonic localization in colorectal cancer with successful detection by laparoscopy, but its benefits remain controversial. This study aimed to assess the accuracy and safety of autogenous blood marker localization in laparoscopic radical resection for colorectal cancer.

Full description

Laparoscopic surgery has become the standard for management of colorectal cancer(CRC) with the advantages of less traumatic procedure, but similar oncological outcomes to open surgery. Due to the lack of tactile perception (haptic feedback), surgeons may have misjudgments in patients with small or flat early colon cancer, malignant polyps resected by endoscopic mucosal resection or endoscopic submucosal dissection. Therefore, the accurate localization of a tumor before surgery is important, especially in the early stages of cancer, to clarify the extent of surgical resection.

Several methods are currently being proposed and used to identify the location of tumors. These include endoscopic tattooing with India ink, indocyanine green (ICG), preoperative endoscopic metal clipping with detection using an x-ray or palpation during surgery, and intraoperative endoscopy.

Recently, some retrospective studies reported the use of patients' autologous blood for preoperative colonic localization in CRC with successful detection by laparoscopy. Autologous blood was thought a feasible and safe tattooing agent for preoperative endoscopic localization. Nonetheless, all currently available evidence comes from observational studies that are susceptible to bias. We therefore proposed to conduct this randomized controlled clinical trial to evaluate the accuracy and safety of autogenous blood marker localization in laparoscopic radical resection for colorectal cancer.

Enrollment

220 estimated patients

Sex

All

Ages

18 to 80 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. Age from 18 to 80 years
  2. Large lateral spreading tumors that could not be treated endoscopically, serosa-negative malignant colorectal tumors (≤ cT3), and malignant polyps treated endoscopically that required additional colorectal resection.
  3. The tumor is located in the colon, middle and high rectum (the lower margin of the tumor does not exceed peritoneal reflexes)
  4. No distant metastasis.
  5. American Society of Anesthesiology score (ASA) class I-III
  6. Performance status of 0 or 1 on Eastern Cooperative Oncology Group scale (ECOG)
  7. Written informed consent

Exclusion criteria

  1. BMI > 35kg/m2
  2. Previous history of gastrointestinal surgery that altered the gastrointestinal anatomy.
  3. Pregnant or lactating women
  4. Severe mental disorder
  5. History of previous abdominal surgery (except cholecystectomy and appendectomy) Rejection of laparoscopic resection
  6. History of cerebrovascular accident within the past six months
  7. History of unstable angina or myocardial infarction within the past six months
  8. History of previous neoadjuvant chemotherapy or radiotherapy
  9. Comorbidity of emergent conditions like obstruction, bleeding or perforation.
  10. Needing simultaneous surgery for other diseases.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

220 participants in 2 patient groups

Autologous Blood Marker Group
Experimental group
Description:
The tattooing was performed at 24-48 hours before the surgery. When the lesion was identified by endoscopy, 2-3 ml of the patient's peripheral venous blood without heparin preparation were injected submucosally at the distal side and proximal side of the lesion using a conventional endoscopic needle without submucosal injection of normal saline.
Treatment:
Procedure: Laparoscopic colorectal cancer resection
Intraoperative colonoscopy group
Active Comparator group
Description:
Under general anesthesia with endotracheal intubation, the patient was placed in the modified lithotomy position. After routine laparoscopic exploration, CO2-insufflated intraoperative colonoscopy was performed using a flexible videocolonoscope. Upstream small bowel clamping was applied before intraoperative colonoscopy. During intraoperative colonoscopy, CO2 pneumoperitoneum was maintained by the insufflator so that the laparoscope could guide the colonoscope effectively.
Treatment:
Procedure: Laparoscopic colorectal cancer resection

Trial contacts and locations

1

Loading...

Central trial contact

Xiao-hua Jiang, MD; Shun Zhang, MD

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems