Feasibility study of opioid-free spontaneous breathing anesthesia technique in day surgery for hand hyperhidrosis

Status

Recruiting

Phases

Early Phase 1

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR2100055005

Enrollment

Unknown

Registered

2021-12-30

Start date

2022-01-10

Completion date

Unknown

Last updated

2023-01-09

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

Conditions

Hand sweat

Interventions

Control group:Strong opioid anesthesia

Weak opioid group:Weak opioid anesthesia

Opioid free group:No opioid anesthesia

Eligibility

Sex/Gender

All

Age

18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Diagnosed as hand hyperhidrosis; 2. To undergo thoracoscopic selective bilateral sympathetic chain amputation; 3. Aged 18-65 years, ASA I-II grade.

Exclusion criteria

Exclusion criteria: 1. Combined with insufficiency of vital organ system; 2. Those with spontaneous bleeding and coagulation disorders; 3. History of chronic pain; 4. Long-term use of opioids or non-steroidal drugs; 5. Those who are allergic to non-steroidal drugs, alcohol, and local anesthetics; 6. Combined with mental illness or cognitive dysfunction; 7. Obesity; 8. Lactation and pregnancy patients; 9. Those who have been diverted to other operations or converted to open surgery.

Design outcomes

Primary

Measure	Time frame
Vital signs;Perioperative complications;Stress hormone level;	—

Secondary

Measure	Time frame
Awakening condition;Discharge time;Satisfaction;	—

Countries

China

Contacts

Public ContactLiu Minqiang

Shenzhen Third People's Hospital

liumq06@sina.com+86 18200981571

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 6, 2026