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A multi-arm parallel controlled randomized clinical study of acupuncture with point selection by pattern identification for the treatment of vocal cord nodules

A multi-arm parallel controlled randomized clinical study of acupuncture with point selection by pattern identification for the treatment of vocal cord nodules

Status
Active, not recruiting
Phases
Phase 1
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2100005349
Enrollment
Unknown
Registered
2021-11-29
Start date
2021-12-05
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

vocal cord nodules

Interventions

2:acupoint selection upon disease
1:Acupuncture therapy:acupoint selection based on syndrome differentiation

Sponsors

Hospital of Chengdu University of Traditional Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
19 Years to 55 Years

Inclusion criteria

Inclusion criteria: Subjects who meet all of the following criteria are eligible for inclusion in this clinical trial: ?Meet the diagnostic criteria of western vocal nodules; ?It conforms to the standard of TCM syndrome diagnosis of vocal nodules (phlegm and blood stasis type); ?Aged between 19 and 55, regardless of gender; ?Cardiovascular diseases, liver and kidney dysfunction and other serious diseases of important organ functions; ?No contraindication of acupuncture; ?The subject is willing to participate in the study, can fully understand the process of the study and the related benefits and possible risks of participating in the study, and has signed the informed consent form.

Exclusion criteria

Exclusion criteria: Subjects meeting any of the following exclusion criteria will not be selected: ?The loss of autonomy; ?Subjects who recently had a cold; ?Subjects with serious primary cardiovascular, lung, kidney, liver, nerve and blood diseases; ?Subjects who have been receiving systemic or topical hormone therapy for the last 1 week ?Subjects with asthma, neurological diseases and hearing impairment; ?Subjects who are needle-sick or unable to receive acupuncture; ?Pregnant or lactating women; ?People with mental illness.

Design outcomes

Primary

MeasureTime frame
VHI-10 scale;

Secondary

MeasureTime frame
Fibrolaryngoscope;GRBAS scale;Acoustic analysis of voice;TCM symptom and sign scale;

Countries

China

Contacts

Public ContactLiZhou
582923616@qq.com18402854869

Outcome results

None listed

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