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Effect of Acupoint Catgut Embedding on Protracted Withdrawal Constipation and Craving in Methamphetamine Addicts Based on fNIRS

Effect of Acupoint Catgut Embedding on Protracted Withdrawal Constipation and Craving in Methamphetamine Addicts Based on fNIRS

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2026001337
Enrollment
Unknown
Registered
2026-05-26
Start date
2026-06-01
Completion date
Unknown
Last updated
2026-06-01

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

Conditions

Stimulant (including amphetamine, methamphetamine, or methcathinone) dependence, in sustained partial remission

Interventions

Sham Acupoint Cagut Embedding Group:Sham Acupoint Cagut EmbeddingSham Acupoint Cagut Embedding

Sponsors

The Second Affiliated Hospital of Yunnan University of Traditional Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 53 Years

Inclusion criteria

Inclusion criteria: Meets the diagnostic criteria for methamphetamine (METH) dependence, with a history of METH abuse of = 6 months. In the protracted withdrawal phase (cessation = 2 weeks), with a withdrawal duration of = 1 month and negative urine drug screen. Meets the Rome IV criteria for functional constipation, with symptoms persisting for = 1 month. Aged 18–52 years, alert and oriented, with stable vital signs, able to cooperate with treatment and examinations. No use of laxatives, antidepressants, or other medications affecting intestinal and central nervous system function in the past month. Voluntarily signs the informed consent form.

Exclusion criteria

Exclusion criteria: Patients with severe cardiac, hepatic, renal, hematological diseases, severe mental disorders or infectious diseases. Patients with organic digestive diseases, skin infections, coagulation disorders or other contraindications for catgut embedding therapy. Patients with a history of impulsive or violent behavior, suicide attempts, epilepsy or organic brain diseases. Patients currently participating in other clinical trials.

Design outcomes

Primary

MeasureTime frame
Constipation symptom score;Drug craving score;

Secondary

MeasureTime frame
Gut Microbiota Detection;Functional Near-Infrared Spectroscopy (fNIRS) Detection;

Countries

China

Contacts

Public ContactLei Pan

Rehabilitation Medicine Department, Second Affiliated Hospital of Yunnan University of Chinese Medicine

119587014@qq.com13608879797

Outcome results

None listed

Source: ITMCTR (via WHO ICTRP) · Data processed: Jun 11, 2026