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The research on the effect of patient controlled epidural analgesia with intermittent bolus technique after combined thoracoscopic-laparoscopic esophagectomy

The research on the effect of patient controlled epidural analgesia with intermittent bolus technique after combined thoracoscopic-laparoscopic esophagectomy

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-INR-17012781
Enrollment
Unknown
Registered
2017-09-24
Start date
2017-10-01
Completion date
Unknown
Last updated
2017-10-02

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

Conditions

esophageal cancer

Interventions

Continuous infusion group:patient controlled epidural analgesia with continuous infusion of ropivacaine and fentany
intermittent administration group:patient controlled epidural analgesia with intermittent bolus of ropivacaine and fentanyl on demond by the patients

Sponsors

First Affiliated Hospital of Chongqing Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. ASA class I to III, aged between 18 and 80 years who were scheduled for thoracoscopic-laparoscopic esophagectomy; 2. No previous history of cardiopulmonary disease; 3. Normal preoperative platelet and coagulant function; 4. No history of spinal trauma, spine malformation and other contraindications of epidural anesthesia.

Exclusion criteria

Exclusion criteria: 1. Patients refusing epidural analgesia; 2. Contraindications to the epidural analgesia as coagulation disorders or infection of the puncture site; 3. Morbid obesity; 4. Pulmonary infection or active asthma; 5. Intellectual disability, inability to comprehend or complete verbal and physical instructions.

Design outcomes

Primary

MeasureTime frame
epidural ropivacaine and fentanyl consumption for postoperative pain treatment;

Secondary

MeasureTime frame
postoperative pain scale;postoperative complications;postoperative ICU stay and postoperative hospital stay;

Countries

China

Contacts

Public ContactKe Wei

First Affiliated Hospital of Chongqing Medical University

962881848@qq.com+86 15902360621

Outcome results

None listed

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