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Observation on the clinical effect of "opening and closing Tiao Shu" acupuncture in the treatment of amyotrophic lateral sclerosis

Observation on the clinical effect of "opening and closing Tiao Shu" acupuncture in the treatment of amyotrophic lateral sclerosis

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2024000212
Enrollment
Unknown
Registered
2024-08-11
Start date
2025-04-01
Completion date
Unknown
Last updated
2024-08-19

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

Conditions

amyotrophic lateral sclerosis

Interventions

"Opening and closing" acupuncture group:Acupuncture plus riluzole
control group: riluzole

Sponsors

The Affiliated Traditional Chinese Medicine Hospital, Guangzhou Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1) meet the above diagnostic criteria; 2) Patients with amyotrophic lateral sclerosis health status Rating (ALS-HSS) of grade 1 to 3; 3) Time of onset < 2 years; 4) Age 18-70 years old; 5) Stable vital signs and normal coagulation function; 6) Good compliance, voluntarily accept acupuncture and cooperate with treatment, complete observation, and family members sign informed consent.

Exclusion criteria

Exclusion criteria: 1) Those who do not meet the above diagnostic and inclusion criteria; 2) Pregnant or lactating women, allergic or allergic to therapeutic drugs. 3) Patients with contraindications to acupuncture and moxibustion, complicated with serious primary diseases such as heart, liver, kidney, hematopoietic system, endocrine system and infectious or infectious diseases; Patients with bleeding tendencies or bleeding disorders; Patients with a history of fainting needles and fainting blood; Patients with severe aphasia, sleep apnea, deafness, severe cognitive impairment and inability to communicate normally; Or are participating in other clinical research trials; 4) Patients who refuse to sign informed consent.

Design outcomes

Primary

MeasureTime frame
ALSFRS-R;

Secondary

MeasureTime frame
SCr\UA\CK;PAC-QOL;

Countries

the People's Republic of China

Contacts

Public ContactChuyun Chen

The Affiliated Traditional Chinese Medicine Hospital, Guangzhou Medical University

chencyzwl@126.com13924026576

Outcome results

None listed

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