Study on mechanism and standardization program of acupuncture (composite) anesthesia on pneumonectomy

Status

Active, not recruiting

Phases

Phase 2

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR-TRC-11001169

Enrollment

Unknown

Registered

2011-01-26

Start date

2008-01-01

Completion date

Unknown

Last updated

2017-04-18

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

Conditions

The mass chest of qualitative and uncertainty

Interventions

E:TEAS2/100 Hz

A:control

B:2Hz

C:2/100Hz

D:100Hz

Eligibility

Sex/Gender

All

Age

30 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Need lung resection surgery, for the first time receiving acupuncture anesthesia surgery; 2. ASA grade I-II level; 3. Aged 30 to 65 years old, male or female; 4. Hospital laboratory examinations have been perfect, past non-immune system diseases; 5. Have signed informed consent; 6. Hospital ethics committee has approval.

Exclusion criteria

Exclusion criteria: 1. The Meridian line passing through the patient after surgery; 2. Meridian skin infections in patients with locally; 3. Upper or lower extremity nerve injury with patients; 4. Nearly four weeks, patients participated in other clinical trials; 5. The patient can not complete the study plan, including language difficulties, infectious diseases and other medical history.

Design outcomes

Primary

Measure	Time frame
NK;TCM syndromes;Electrolyte;5 - hydroxytryptamine;Blood gas analysis;dynorphin;Light - enkephalin;Ts;Physical type;Glucose;Substance P;IL-6;IL-1;Physiological Index;Bradykinin;Epinephrine;Dose of Fentanyl;Pain threshold /Pain tolerance threshold;Dose of Propofol;	—

Countries

China

Contacts

Public ContactWeidong Shen

shenweidong1018@hotmail.com+86 13818288281

Outcome results

None listed

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