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Feasibility of certain surgical operations under general anesthesia without muscle relaxant

Feasibility of certain surgical operations under general anesthesia without muscle relaxant

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-TRC-10000854
Enrollment
Unknown
Registered
2010-04-26
Start date
2010-05-01
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

surgery related diseases

Interventions

Group A:General anesthesia will be induced with midazolam, fentanyl, scoline and propofol, and maintained with remifentanil, atracurium, propofol.
Group B:Anesthesia will be induced using the same protocol as that in the control group, but maintained with remifentanil and propofol.

Sponsors

The First Hospital of Lanzhou University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Patients aged from 18 to 80 years old with preoperative ASA grade I or II; 2. Undergoing a non-abdominal operation using general anesthesia; 3. No history of drug addiction, central or peripheral nervous system pathology, vegetarian nervous disorders or nerve-muscle adaptor lesions. No history of autoimmune diseases or familial genetic diseases; 4. Agreed to participate in orally before operation or sign the informed consent form.

Exclusion criteria

Exclusion criteria: 1. Unwilling to participate in or refuse to sign an informed consent form; 2. Patients with blood loss more than 30% of total blood volume during operation, or with anemia (Hb lower than 90 g/L) ; 3. Hypotention(sBP<12 Kpa) persist more than 5 min, hypoxia (SpO2<=90%) persist more than 30 seconds or pernicious arrhythmia, cardiac arrest or other unexpected accidents occur during operations; 4. Patients be found allergy to anesthetics, or have family history of malignant hyperthermia; 5. Operations are affected by muscle tension, body movement or other circumstances.

Design outcomes

Primary

MeasureTime frame
Recovery time, body movement;BIS,TOF;MAP, HR, SPO2;

Secondary

MeasureTime frame
Anesthetics dosage, anesthesia expense;

Countries

China

Contacts

Public ContactYulan Li
jasm@sina.com.cn+86 13519625065

Outcome results

None listed

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