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Effect of paravertebral nerve block on intestinal injury associated with Pringle manipulation in liver surgery

Study on the protective effect and mechanism of Pringle maneuver related intestinal injury in liver surgery improved by paraspinal nerve block

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400094425
Enrollment
Unknown
Registered
2024-12-23
Start date
2025-01-01
Completion date
Unknown
Last updated
2025-01-06

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

Conditions

Gastrointestinal environment disorders, mucosal barrier disorders and related diseases

Interventions

PVB group:Unilateral paravertebral nerve block at four points (0.375% ropivacaine, 15ml at each point) was received 30min before surgery
Control group:No block operation was performed before surgery, and other operations were the same as those in PVB group

Sponsors

Fujian Provincial Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1) Patients aged 18-65 years who plan to undergo elective open hepatectomy; 2) American College of Anesthesiologists (ASA) Levels I to III; 3) AGI grade 0 before operation, with no gastrointestinal related underlying diseases; 4) Sign informed consent voluntarily.

Exclusion criteria

Exclusion criteria: 1) 65 years old; 2) Contrainidators for paravertebral block treatment: skin infection or ulceration on the body surface of the back, spinal or thoracic deformity, spinal cord injury above the T10 level, allergy to amide local anesthetics, etc; 3) Significant abnormal coagulation function: platelet count 65s; 4) any neurological or mental illness, including a history of substance abuse, anxiety or depression, or treatment; 5) Special personnel, such as pregnant women, brain death patients; 6) The patient plans to undergo additional gastrointestinal surgery; 7) Unable to cooperate with the study for any reason, such as difficulty in language understanding, refusal to participate in the study, etc.

Design outcomes

Primary

MeasureTime frame
Improvement rate of postoperative gastrointestinal function score ;

Secondary

MeasureTime frame
ntestinal fatty acid binding protein(I-FABP);Visual Analogue Scale(VAS) ;

Countries

China

Contacts

Public ContactDanfeng Wang

Fujian Provincial Hospital

251487848@qq.com+86 139 0692 0551

Outcome results

None listed

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