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Assessing the efficacy of thoracolumbar interfascial plane block for perioperative analgesia in patients with postherpetic neuralgia

Assessing the efficacy of thoracolumbar interfascial plane block for perioperative analgesia in patients with postherpetic neuralgia

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400087085
Enrollment
Unknown
Registered
2024-07-19
Start date
2024-03-12
Completion date
Unknown
Last updated
2024-07-22

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

Conditions

postherpetic neuralgia

Interventions

Ultrasound guided bilateral thoracolumbar fascia plane block group:Bilateral thoracolumbar fascia plane block is performed under ultrasound guidance
control group:nothing

Sponsors

Department of Pain, the First Affiliated Hospital of Anhui Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 85 Years

Inclusion criteria

Inclusion criteria: (1) PHN: There is a history of herpes zoster and the pain lasts for more than 1 month after healing of herpes lesions; (2) The pain relief was not obvious after treatment with standard analgesic drugs, and the VAS score was > 3 points, with a full score of 10; (3) 18= age =85 years old, gender is not limited; (4) Can cooperate with the evaluation of pain, sleep and other scales; (5) Exclude pain caused by other causes; (6) Voluntarily participate in the study and sign the informed consent.

Exclusion criteria

Exclusion criteria: (1) Severe impairment of heart, lung, liver and kidney function; (2) Psychiatric disorders: such as schizophrenia, depression, history of chronic analgesic medication, history of alcoholism, opioid dependence, or inability to understand visual analog scores; (3) Endocrine system diseases: pituitary tumor, severe diabetes, hypercortisolism, pheochromocytoma, etc (4) Patients who had received spinal cord electrical stimulation before admission; (5) The nerve in the affected area has been damaged before; (6) Other treatment methods after discharge; (7) Pregnant woman or puerpera ; (8) Lost visitors.

Design outcomes

Primary

MeasureTime frame
visual analogue scale;

Secondary

MeasureTime frame
Quality-of-recovery 15;mean arterial pressure;heart;

Countries

CHINA

Contacts

Public ContactLikui Wang

Department of Pain, the First Affiliated Hospital of Anhui Medical University

wlk9560@163.com+86 137 0569 0702

Outcome results

None listed

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