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Comparison of Three Analgesia Monitoring Methods under Laparoscopic Surgery:prospective single-arm trial

Comparison of Three Analgesia Monitoring Methods under Laparoscopic Surgery:prospective single-arm trial

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR-ROC-17013492
Enrollment
Unknown
Registered
2017-11-22
Start date
2017-12-01
Completion date
Unknown
Last updated
2017-11-27

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

Conditions

Abdominal diseases

Interventions

one group:change remifentanil infusion concentration

Sponsors

The Second Affiliated Hospital and Yuying Children's Hospital of Wenzhou Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. ASAI, Level II; 2. Aged 18-65 years; 3. BMI: =25; 4. Patients or Authorized Signatories Informed Consent Form

Exclusion criteria

Exclusion criteria: 1. heart disease (specifically to place pacemakers, frequent arrhythmias, etc.); 2. lung disease (specifically pulmonary infection, emphysema, chronic obstructive pulmonary disease, etc.); 3. Allergic; 4. known to be difficult airway; 5. preoperative hemoglobin concentration, hematocrit (Hct) is not within the normal range; 6. renal impairment (BUN and / or Cr> upper limit of normal); 7. liver function impairment (ALT and / or AST> 1.5 times normal reference range); 8. suffering from mental, neurological diseases, or can not properly express the wishes of patients; 9. long-term use of sedative and analgesic, psychotropic drugs; 10. coagulation disorders (PT / APTT higher than the upper limit of the reference value); 11. arm disability, blood pressure and oxygen saturation monitoring can only be located on the same side of the arm; 12. history of hypertension and blood pressure systolic blood pressure> 180 or diastolic blood pressure> 110mmHg two measurements Did not decline; 13.neuromuscular diseases (specifically paraplegia, myasthenia gravis).

Design outcomes

Primary

MeasureTime frame
SPI;response entropy;PRi;

Secondary

MeasureTime frame
Heart rate;blood pressure;

Countries

China

Contacts

Public ContactHan Lin

The Second Affiliated Hospital and Yuying Children's Hospital of Wenzhou Medical University

nanlinhannansh@qq.com+86 15868710831

Outcome results

None listed

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