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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05517681
Other study ID # 20210130
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date September 7, 2020
Est. completion date July 10, 2022

Study information

Verified date August 2022
Source The First Hospital of Qinhuangdao
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Indocyanine green NIR imaging is valuable for lymph node dissection in D3 radical surgery for rectal cancer. It can guide the intraoperative improvement of lymph node dissection based on the preservation of LCA and peripheral autonomic nerves of IMA. This not only reduces the occurrence of postoperative complications and promotes rapid postoperative recovery, but also provides a more precise and individualized comprehensive treatment plan for patients after surgery. In addition,this trial also demonstrated that ICG is safe and feasible for use in rectal cancer


Description:

The pathological data of 96 patients with rectal cancer from September 2020 - July 2022 were collected from the First Hospital of Qinhuangdao City.In 51 of these patients, ICG was injected preoperatively via anoscope or anal dilator in the mucosal layer around the tumor, and surgical treatment was performed after visualization. The surgical approach was performed by laparoscopic radical rectal cancer with an intermediate approach step.The IMA root is treated with low ligation of the IMA, while lymph node dissection is performed while preserving the autonomic nerves around the IMA. The other 45 patients were not injected with ICG, and the procedure was performed as before.The occurrence of postoperative complications was recorded, and the detection of lymph nodes was also compared between the two groups, as well as the intraoperative situation and postoperative recovery.


Recruitment information / eligibility

Status Completed
Enrollment 96
Est. completion date July 10, 2022
Est. primary completion date July 10, 2022
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 40 Years to 80 Years
Eligibility Inclusion Criteria: 1. The preoperative colonoscopic pathological diagnosis was clearly rectal cancer and no malignant tumor in other sites. 2. Good preoperative general condition, no serious cardiopulmonary, hepatic, renal or other major comorbidities before surgery 3. Radical rectal cancer surgery with preservation of LCA and peripheral autonomic nerves of IMA in patients 4. No contraindications to surgery 5. No history of ICG or iodide allergy Exclusion Criteria: -

Study Design


Related Conditions & MeSH terms


Intervention

Other:
non-ICG
Laparoscopic radical resection of rectal cancer was performed routinely without ICG injection. The separation should extend from the center to the left, reaching the left paracolic sulcus lateral to the genital vessels. The Superior hypogastric nerve is protected by freeing it at the angle of the common iliac artery on both sides, afterwards, the vessel is free along the surface of the plexus from caudal to cephalic side to reach the root of the IMA. Switching lymph node visualization patterns. Based on the operator's experience and the extent of lymph node visualization, the lymph nodes at the root of the IMA were removed with an ultrasonic knife . The dissection continues caudally along the IMA, preserving the arterial sheath. Expose the left colonic artery, superior rectal artery, and sigmoid artery, maximum preservation of the IMA peripheral plexus while clearing their surrounding lymph nodes.
Drug:
ICG
Dilute ICG to 2.5 mg/ml with its accompanying sterilized water for injection. Slow injection with a 1ml syringe in 4 parts of the tumor,Inject 0.25ml per site . Procedure started after lymph node visualization.The operation was consistent with the control group.

Locations

Country Name City State
China The First hosptial of Qinhuangdao Qinhuangdao

Sponsors (1)

Lead Sponsor Collaborator
The First Hospital of Qinhuangdao

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary The number of cleared IMA root lymph nodes A group of lymph nodes surrounding the inferior mesenteric artery between the origin of the artery and the left colic artery immediately after surgery
Primary The total number of cleared lymph nodes The sum of IMA root lymph nodes and lymph nodes surrounding the tumor area immediately after surgery
Primary The number of positive lymph nodes There are metastatic tumor cells in the lymph nodes immediately after surgery
Secondary Quality of postoperative recovery days of postoperative hospitalization, days of retention of the urinary catheter, days of retention of abdominal drainage tube, time of first fluid intake and IPSS score Up to 7 days after surgery
Secondary The incidence of postoperative complications mild or severe urogenital disorders, anastomotic leakage, anastomotic bleeding, abdominal infection, intestinal obstruction. Up to 7 days after surgery
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