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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05674097
Other study ID # 2020GQliu
Secondary ID
Status Completed
Phase
First received
Last updated
Start date June 8, 2020
Est. completion date March 31, 2022

Study information

Verified date December 2022
Source Shandong First Medical University
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

89 patients with distal sigmoid and rectal cancer were referred in our observation and underwent MS-CTA between June 2020 and March 2022. We classified the distribution of LCA and confirmed whether there exists AMCA (accessory middle colic artery). Then we planned blood flow path based on the classification of LCA branches before operation. High ligation was applied in regular radical surgery. During operation, we carefully protect the bifurcation of ascending and descending LCA. Then we compared the planned blood flow path with the actual postoperative blood flow path to verify the mechanism we proposed previously.


Recruitment information / eligibility

Status Completed
Enrollment 89
Est. completion date March 31, 2022
Est. primary completion date March 8, 2022
Accepts healthy volunteers
Gender All
Age group 39 Years to 81 Years
Eligibility Inclusion Criteria: - (1) patients with distal sigmoid colon and rectal cancer; (2) cTNM stage was confirmed to be I-III on MRI or CT; (3) Laparoscopic anterior resection (LAR) was performed. Exclusion Criteria: - (1) The starting time of arterial phase scanning is earlier; (2) The anatomic structure is not clear; (3) No enhanced CT after operation (only 5 cases).

Study Design


Related Conditions & MeSH terms


Intervention

Other:
no intervention
no intervention

Locations

Country Name City State
China Guoqin LIU Jinan Shandong

Sponsors (2)

Lead Sponsor Collaborator
Guoqin LIU Jinan Central Hospital

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary Six pattens of blood flow and AMCA based on the preoperative observation 1 hour
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