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Establishment and application of Q-1064nm laser treatment mode for refractory postherpetic neuralgia

Establishment and application of Q-1064nm laser treatment mode for refractory postherpetic neuralgia

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200066191
Enrollment
Unknown
Registered
2022-11-28
Start date
2022-12-01
Completion date
Unknown
Last updated
2023-05-15

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

Conditions

postherpetic neuralgia

Interventions

Experimental group:Q(1064nm) Laser treatment
Control group:Q(532nm) Laser treatment

Sponsors

Xijing Hospital, Fourth Military Medical University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Age over 18, regardless of gender; 2. Patients with clinical diagnosis of chronic post herpetic neuralgia were judged to be stable by the researchers; 3. The routine treatment such as medicine is ineffective or the remission is not obvious; 4. The pain rating is more than 3 points according to the overall evaluation standard of the researcher; 5. Before the trial, the subject must sign the informed consent form.

Exclusion criteria

Exclusion criteria: 1. Known hypersensitivity to laser spectrum; 2. Patients in acute stage 3. People with serious heart, kidney, liver, endocrine and other system diseases or with tumor and immune deficiency diseases; 4. Those who have received phototherapy, systematic drug therapy and interventional therapy with allergic reaction before the study; 5. Those who are currently participating in other clinical studies or have participated in other clinical studies within 3 months; 6. According to the judgment of the researcher, the guardian is not credible or has poor compliance. 7. Pregnant women or women with fertility plan to be pregnant or lactating during the trial period; 8. For those who are known or suspected to have poor compliance and can not complete the test, such as alcoholism, drug dependence or mental illness, the investigator judges that they are not suitable to participate in this clinical study.

Design outcomes

Primary

MeasureTime frame
Visual Analogue Scale;IL- 6;substance P;ß-endorphin;

Countries

China

Contacts

Public ContactFan Xing

Xijing Hospital, Fourth Military Medical University

fanxing.612@163.com+86 18629391111

Outcome results

None listed

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