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Application of Ultrasound-Mediated Targeted Drug Delivery in Postoperative Rehabilitation after Hepatobiliary Surgery

Application of Ultrasonic Targeted Drug Therapy in Postoperative Rehabilitation of Hepatobiliary Surgery

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2026000016
Enrollment
Unknown
Registered
2026-01-04
Start date
2024-09-11
Completion date
Unknown
Last updated
2026-01-12

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

Conditions

Hepatobiliary surgery cases (including gallstone disease, gallbladder polyps, gallbladder adenomyosis, hepatic cysts, hepatic hemangiomas, hepatic focal nodular hyperplasia, and others)

Interventions

blank control group:Placebo patch application + Simulated ultrasound-guided targeted drug delivery
Patch Group:Chinese and Western medicine patch application + simulated ultrasound-mediated targeted drug
Ultrasonic Group:Integrated Chinese and Western Medicine Patch Application + Real Ultrasound-Guided Targeted Drug Delivery

Sponsors

Jiangnan University Affiliated Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: (1) Liver and biliary surgery cases (including cholecystolithiasis, cholecystic polyps, adenomyomatosis of the gallbladder, hepatic cysts, hepatic hemangiomas, focal nodular hyperplasia of the liver, etc.), with biochemical tests indicating total bilirubin, transaminases < 2 ULN; (2) Age 18-70 years, without severe heart, lung, brain, liver, kidney, vascular, hematological, or mental diseases; (3) American Society of Anesthesiologists (ASA) classification I–II; (4) Smooth surgical procedure, stable vital signs, no blood transfusion; (5) Subjects agree to participate in the clinical study and sign the informed consent, and the study has been reviewed and approved by the hospital's ethics committee (LS2024350).

Exclusion criteria

Exclusion criteria: (1) history of chronic diarrhea, constipation, inflammatory bowel disease, gastrointestinal tumors, or cardiac pacemaker implantation; (2) severe obesity or malnutrition (BMI > 30 kg/m2 or < 15 kg/m2); (3) history of gastrointestinal or abdominal surgery; (4) use of gastrointestinal motility drugs within one month before surgery; (5) patients with comorbidities such as allergies, rashes, anemia, anxiety, depression, and other difficult-to-correct physical and mental illnesses.

Design outcomes

Primary

MeasureTime frame
Time to first postoperative flatus;

Secondary

MeasureTime frame
Postoperative recovery time of bowel sounds.;Postoperative first bowel movement time;Postoperative tolerance time for semi-liquid diet;Postoperative nausea and vomiting incidence rate;24h postoperative abdominal circumference change;24h postoperative VAS pain score;Postoperative 24h core body temperature;Postoperative self-ambulation time;Postoperative 48-hour period psychological depression SDS score;Postoperative 48-hour recovery quality QoR-15 score;Postoperative hospital stay;Serum interleukin-6 (IL-6);Serum Adrenaline (AD);Serum prealbumin;

Countries

China

Contacts

Public ContactChen Enhong

Jiangnan University Affiliated Hospital

enhomchen522009@163.com15861588020

Outcome results

None listed

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