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Trial · NCT06798662

Multimodal Nerve Block and Pulse Radiofrequency for Acute Herpes Zoster Pain

NCT06798662, Not applicable, Not yet recruiting, Xiaguang Duan

3 sourcestrials-2026-11-12-0.4.0

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ConductScience Library. Multimodal Nerve Block and Pulse Radiofrequency for Acute Herpes Zoster Pain. Trials, record NCT06798662. Release trials-2026-11-12-0.4.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT06798662

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Trial

As registered on ClinicalTrials.gov, in the graph's capture of the registry.

Title
Multimodal Nerve Block and Pulse Radiofrequency for Acute Herpes Zoster Pain
NCT number
NCT06798662
Status
Not yet recruiting
Phases
Not applicable
Enrollment
120 participants, estimated
Lead sponsor
Xiaguang Duan
Conditions
Herpes Zoster (HZ)
Interventions
Ultrasound-Guided Pulsed Radiofrequency (PRF), Intercostal nerve block (2% ropivacaine or 133 mg of liposomal bupivacaine), Paravertebral (PVB) Block (2% ropivacaine or 133 mg of liposomal bupivacaine), Rhomboid Intercostal and Subserratus Plane (RISS) Block (2% ropivacaine or 133 mg of liposomal bupivacaine), Drug (famciclovir and gabapentin)
First posted
2025-01-29
Last updated
2025-01-29

Source ClinicalTrials.gov

Registered outcomes2

Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.

ListOutcomeTime frameDescription
PrimaryNumerical Rating Scale(NRS)At baseline (before therapy), at 1 day of treatment, at 7 days post-treatment, 30 days post-treatment, and 90 days post-treatmentThe NRS, Numerical Rating Scale, is a rating system from 0 to 10, where 0 represents "no pain" and 10 represents the worst possible pain.
SecondaryThe Zoster Brief Pain Inventory (ZBPI)At baseline (before therapy), at 1 day of treatment,, at 7 days post-treatment, 30 days post-treatment, and 90 days post-treatment
The Zoster Brief Pain Inventory (ZBPI) was used as the HZ-specific pain measure. The daily activity questionnaire included seven items: general activity, mood, walking ability, normal work, relationships with others, sleep, and enjoyment of life. Each question concerning daily activity was scored on a scale from 0 to 10, where 0 indicated no interference and 10 indicated complete interference.

Outcomes0

Each outcome the trial posted results for, in ClinicalTrials.gov's words.

None in this release.

Results by group0

Each measurement the trial posted, group by group, in the words and numbers it posted.

None in this release.

Participant flow0

How many started, completed or left each group, period by period.

None in this release.

Adverse events0

Each adverse event the trial posted, group by group: the participants affected out of those at risk.

None in this release.

Adverse event totals0

The totals the trial posted for each group.

None in this release.

Papers10

The papers the trial lists on ClinicalTrials.gov.

PMIDListed asSource
19680122BACKGROUNDPubMed
31741185BACKGROUNDPubMed
34283910BACKGROUNDPubMed
35215786BACKGROUNDPubMed
36300903BACKGROUNDPubMed
36539935BACKGROUNDPubMed
36880287BACKGROUNDPubMed
37468840BACKGROUNDPubMed
38009329BACKGROUNDPubMed
38981512BACKGROUNDPubMed

Grants0

The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.

None in this release.

Trial comparisons0

Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.

None in this release.

Tests0

The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.

None in this release.

Source

Release
trials-2026-11-12-0.4.0
Release manifest SHA-256
0f4a8d8c48aee2a7573ae0fa94ecbeab70c1adbe449bbc95c424bc7d3e97b9d4
Registry capture
2026-11-12
Results copy, AACT
2026-03-23
NIH clinical studies file
2026-11-13

Source ClinicalTrials.gov

Sources 3

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNone stated
  • NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
  • ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
  • ClinicalTrials.govnone stated
  • NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

For software

Read this trial from software.

The record and each of its lists are JSON, twenty rows a page. No key.

GET https://conductscience.org/api/trials/v1/NCT06798662

GET https://conductscience.org/api/trials/v1/NCT06798662/registered