Platelet-rich Plasma in the Treatment of Intractable Postherpetic Neuralgia

NCT ID: NCT05444413

Last Updated: 2022-09-08

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

PHASE1

Total Enrollment

32 participants

Study Classification

INTERVENTIONAL

Study Start Date

2022-03-03

Study Completion Date

2022-07-01

Brief Summary

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used ultrasound-guided platelet rich plasma nerve block to treat Intractable Postherpetic Neuralgia.

Detailed Description

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Postherpetic neuralgia (PHN) is a kind of pain caused by varicella zoster virus invading the human body and infecting the corresponding ganglia. The affected ganglia are inflamed or even necrotic, affecting the nerve endings, the dorsal horn of the spinal cord and the sensory nerve tissues below, and the course of the disease is more than one month or more. Most patients can avoid PHN by timely and effective treatment in the acute herpes zoster period. However, some patients with intractable postherpetic neuralgia fail to receive timely and effective pain control treatment in the early stage of the disease, and the current commonly used clinical treatment methods often fail to achieve effective treatment results. Such patients often have a long course of disease, which can last for three to five years or even longer, Nerve damage is also more serious. Long term pain has seriously affected the quality of life of such patients. Therefore, how to quickly and effectively control pain has become the diagnosis and treatment goal of such patients with intractable post herpetic neuralgia. Platelet rich plasma (PRP) was widely used in muscle and bone repair due to its function of promoting tissue repair in the early stage. Recently, it was found that PrP can also promote nerve repair. Therefore, in order to further explore the therapeutic effect of PRP on refractory PHN patients, our department used ultrasound-guided platelet rich plasma nerve block to treat Intractable PHN.

Conditions

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PHN - Post-Herpetic Neuritis

Study Design

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Allocation Method

NA

Intervention Model

SINGLE_GROUP

patients with Intractable Postherpetic Neuralgia
Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

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ultrasound-guided platelet rich plasma nerve block combined with drugs

selected patients were treated by the ultrasound-guided platelet rich plasma nerve block once a week for the 4 consecutive weeks while they were given the regular medicine which are taking pregabalin and amitriptyline hydrochloride orally, and the dosage shall be increased or decreased according to the patient's condition.

Group Type EXPERIMENTAL

ultrasound-guided platelet rich plasma nerve block

Intervention Type BIOLOGICAL

selected persons are treated by ultrasound-guided platelet rich plasma nerve block and the regular medicine

Interventions

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ultrasound-guided platelet rich plasma nerve block

selected persons are treated by ultrasound-guided platelet rich plasma nerve block and the regular medicine

Intervention Type BIOLOGICAL

Eligibility Criteria

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Inclusion Criteria

* Meet the diagnostic criteria of PHN: have a history of acute herpes zoster, the pain lasts for more than half a year, and there is paroxysmal pain in the affected nerve distribution area;
* Preoperative visual analog scale (VAS) score ≥ 5;
* Those who can cooperate with the treatment;
* We agreed to inject platelet rich plasma into nerve block under the guidance of ultrasound, and signed the informed consent form.

Exclusion Criteria

* Systemic infection or puncture local infection;
* Serious disturbance of cardiovascular and cerebrovascular function;
* Abnormal bleeding and coagulation function or complicated with blood system diseases;
* Mental disorders;
* Severe dysfunction of important organs in the body
Minimum Eligible Age

40 Years

Maximum Eligible Age

70 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Affiliated Hospital of Nantong University

OTHER

Sponsor Role lead

Responsible Party

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Yuan Zhou

Deputy chief physician

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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yuan zhou, doctor

Role: STUDY_DIRECTOR

Affiliated Hospital of Nantong University

Locations

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Affiliated Hospital of Nantong University

Nantong, Jiangsu, China

Site Status

Countries

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China

Other Identifiers

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2022-K036

Identifier Type: -

Identifier Source: org_study_id

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