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Effect of target-controlled infusion of different concentrations of remifentanil combined with propofol on CSI and postoperative recovery in patients undergoing laparoscopic total hysterectomy

Effect of target-controlled infusion of different concentrations of remifentanil combined with propofol on CSI and postoperative recovery in patients undergoing laparoscopic total hysterectomy

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400085516
Enrollment
Unknown
Registered
2024-06-11
Start date
2024-07-01
Completion date
Unknown
Last updated
2024-07-08

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

Conditions

disease of uterus

Interventions

RL Group:Remifentanil 2 µg/L
The initial propofol effect chamber concentration during the anesthesia maintenance phase for the first patient in each group is 2 mg/L. The propofol concentration for each subsequent patient is deter
On the contrary, it will decrease by 0.5 mg/L.
RM Group:Remifentanil 4 µg/L
RH Group:Remifentanil 6 µg/L

Sponsors

The First Affiliated Hospital of USTC
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
30 Years to 65 Years

Inclusion criteria

Inclusion criteria: Patients undergoing gynecological laparoscopic hysterectomy under general anesthesia; American Society of Anesthesiologists (ASA) grade I-II; The age ranged from 30 to 65 years; Body mass index (BMI) : 18.5-29 kg/m2

Exclusion criteria

Exclusion criteria: poor compliance, unable to cooperate with the operation; with serious organic lesions (coronary heart disease, bronchial asthma, severe hypertension, severe blood system dysfunction, liver and kidney function, significant electrolyte abnormalities); II and above atrioventricular block, bradycardia (HR < 50 min/time), hypotension (SBP < 90mmHg); History of nervous system; A history of chronic pain; Drug addiction and alcohol abuse; A long history of opioid use; History of opioid allergy; patients with limited gastric emptying and gastroparesis; Patients with slow peristalsis and intestinal obstruction; those who participated in clinical trials of other drugs within the past 4 weeks; patients with other conditions considered by the investigator to be ineligible for inclusion.

Design outcomes

Primary

MeasureTime frame
Duration of awakening;

Secondary

MeasureTime frame
MAP;Heart rate;Duration of surgery;BIS;cerebral state index;

Countries

China

Contacts

Public ContactHe keqiang

The First Affiliated Hospital of USTC

doctorhector@ustc.edu.cn+86 189 5519 7569

Outcome results

None listed

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