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Trigger point dry needling in the treatment of postherpetic neuralgia: a prospective, randomized controlled study

Trigger point dry needling in the treatment of postherpetic neuralgia: a prospective, randomized controlled study

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2100004300
Enrollment
Unknown
Registered
2021-01-21
Start date
2021-01-21
Completion date
Unknown
Last updated
2023-02-20

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

Conditions

postherpetic neuralgia

Interventions

dry needling group:conventional therapy + dry needle
placebo-needling group:conventional therapy + placebo needle

Sponsors

The First Affiliated Hospital of Jinan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: (1) The diagnosis of postherpetic neuralgia was based on the "Chinese Expert Consensus on the Diagnosis and Treatment of postherpetic neuralgia". (2) Visual analogue scale(VAS) of pain score above 4. (3) No contraindications or intolerable adverse reactions to neuropathic pain drugs, such drugs include: pregabalin, amitriptyline, opioids (tramadol, morphine, oxycodone, etc.). (4) Premenopausal women are willing to confirm birth control measures during the trial. (5) No other treatment will be given during the trial. (6) Have normal comprehension and expression ability.

Exclusion criteria

Exclusion criteria: (1) Patients with other severe chronic pain. (2) Initiate additional treatment during the trial. (3) The patient is pregnant or nursing. (4) Patients with drug or alcohol dependence. (5) Mental illness that affects patients' judgment or interferes with the conduct of the trial. (6) Unwilling to accept the review or unable to understand the scale measurement. (7) Patients with nausea tumor (except patients without recurrence 6 months after radical surgery). (8) Patients with abnormal coagulation function. (9) Patients with acute thrombotic events: ischemic stroke, myocardial infarction, pulmonary embolism, deep venous thrombosis, etc. (10) Unstable angina pectoris. (11) Renal insufficiency (serum creatinine 1.5 times higher than the normal high value). (12) The Investigator considers that there are any conditions that could pose a medical risk or affect the outcome of the trial. (13) Participate in other medical trials during the study period.

Design outcomes

Primary

MeasureTime frame
VAS score;

Secondary

MeasureTime frame
Short-form McGill Pain questionnaire;the Patient Health Questionnaire-9 (PHQ-9);Short Form-36 Health Survey (SF-36);Pittsburgh Sleep Quality Index (PSQI);Generalized Anxiety Disorder Scale (GAD-7);

Countries

China

Contacts

Public ContactXiaoping Wang

The First Affiliated Hospital of Jinan University

txp2938@jun.edu.cn+86 18903078576

Outcome results

None listed

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