Clinical study on sequential method and minimally invasive treatment of intestinal fistula based on B-ultrasonic precision positioning

Status

Active, not recruiting

Phases

Phase 1

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR2000036344

Enrollment

Unknown

Registered

2020-08-22

Start date

2020-10-01

Completion date

Unknown

Last updated

2020-09-07

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

Conditions

Intestinal fistula

Interventions

Control group (open surgery):Open surgery

Traditional laparoscopic group:Traditional laparoscopic technique

B-Ultrosonic location group:B-Ultrosonic location before laparoscopic surgery

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: 1. Patients with a diagnosis of intestinal fistula, admitted by or transfer to our hospital; 2. Patients aged between 18 and 80 years old; 3. Patients with no malignant tumor; 4. With signed informed consent from the patients and their next of kin.

Exclusion criteria

Exclusion criteria: 1. Patients receiving chemo or radioactive therapy for active malignant tumor; 2. Patients in other clinical trial; 3. Females that are pregnant or lactating; 4. Patients who refuse or can not sign on informed consent; 5. Patients who can not follow the experimental plan; 6. Patients on glucocorticoid or other immunosuppressant.

Design outcomes

Primary

Measure	Time frame
mortality;quality of life score;length of stay after surgery;medical costs;	—

Secondary

Measure	Time frame
APACHE II score;Mortality in 28 days and total mortality;total length of stay;	—

Countries

China

Contacts

Public ContactChen Chunqiu

Shanghai Tenth People's Hospital

chenchunqiu6@126.com+86 13671864838

Outcome results

None listed

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