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A clinical study on the effectiveness and safety of different epidural administration methods led by SMT nurses for pain management in SAP (Severe Acute Pancreatitis)

A clinical study on the effectiveness and safety of different epidural administration methods led by SMT nurses for pain management in SAP (Severe Acute Pancreatitis)

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500101922
Enrollment
Unknown
Registered
2025-05-06
Start date
2025-05-15
Completion date
Unknown
Last updated
2025-05-12

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

Conditions

Severe acute pancreatitis

Interventions

Control group:Continuous TEA using a drug combination of: nalbuphine 40 mg + ropivacaine 225 mg + lidocaine 0.2 g + 0.9% saline 6 ml in a total volume of 50 ml at an infusion rate of 3-5 ml/h. When th
Experimental group:On the basis of continuous TEA, the pain management nurse led the TEA management strategy based on STM, and when the patients VAS-P exceeded a score of 3 or pain was intolerable, an

Sponsors

Affiliated Hospital of Zunyi Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Patient age>=18 years. 2. Patients with a clear diagnosis of SAP. 3. Pain score greater than 3 points. 4. Need for effective epidural analgesic pain management. 5. The patient or his/her legal representative signs the informed consent form.

Exclusion criteria

Exclusion criteria: 1. Patients with contraindications to epidural analgesia, such as coagulation dysfunction, local infection, allergy to lidocaine, etc. Combined with severe heart, lung, liver, renal failure, severe infection, malignant diseases and autoimmune diseases. 2. Patients with pancreatic pseudocyst and infection. 3. Patients who voluntarily sign off and are discharged during the ICU hospitalization or throughout the hospitalization. 4. Patients with incomplete medical records.

Design outcomes

Primary

MeasureTime frame
Visual Assessment Scale-Pain (VAS-P);

Secondary

MeasureTime frame
Intra-abdominal pressure (IAP);Dosage of combined drugs(DCD;Number of additional interventions(NAI);Number of days of epidural placement(NDEP);

Countries

China

Contacts

Public ContactYou Yuan

Affiliated Hospital of Zunyi Medical University

yuanyou94@foxmail.com+86 187 9812 0470

Outcome results

None listed

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