Skip to content

Comparative study of endoscopic tattooing using sodium hyaluronate solution of rectal tumors

Comparative study of endoscopic tattooing using sodium hyaluronate solution of rectal tumors

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000034124
Enrollment
Unknown
Registered
2020-06-25
Start date
2020-06-16
Completion date
Unknown
Last updated
2020-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Rectal tumors

Interventions

control group:Submucosal injection normal saline
experimental group:Submucosal injection of low concentration of sodium hyaluronate
experimental group:Submucosal injection of medium concentration of sodium hyaluronate
experimental group:Submucosal injection of high concentration of sodium hyaluronate

Sponsors

Digestive Department of the 900th Hospital of the Joint Service Support Force, People's Liberation Army 900th Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Patients between 18 and 80 years old; 2. Patients with rectal cancer confirmed by pathological biopsy and to be operated; 3. Patients with preoperative clinical stage of early rectal cancer (TNM stage within T2 or T3 limited in the mesorectum); 4. Patients who agree and sign informed consent.

Exclusion criteria

Exclusion criteria: Any of the following shall be excluded: 1. Patients who did not receive surgical treatment due to tumor stage, physical condition, economy and other reasons; 2. Patients who have received radiotherapy, neoadjuvant chemotherapy and biotherapy before operation; 3. There are patients who need operation or endoscopic stent implantation for intestinal obstruction and perforation; 4. Patients who dropped out of the study for other reasons.

Design outcomes

Primary

MeasureTime frame
visibility rate; Area of black spot on serous surface;endoscopic tattooing duration;

Secondary

MeasureTime frame
Total duration of operation;Intraoperative bleeding volume;The distance between the edge of the tumor and the anastomosis;Complication;

Countries

China

Contacts

Public ContactRong Wang

Fujian Medical University

ronglittle2003@163.com+86 13959119903

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026