Epidural Anesthesia-analgesia and Long-term Outcome

NCT03012945 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 1802

Last updated 2020-07-08

No results posted yet for this study

Summary

Surgical resection is one of the most important treatments for resectable cancer; on the other hand, cancer recurrence and/or metastasis are the major reasons of treatment failure. The development of recurrence/metastasis after cancer surgery mostly depends on the balance between the immunity of human body and the capability of implantation, proliferation and neovascularization of the residual cancer. Preclinical and retrospective clinical studies suggest that anaesthetic management may affect the long-term outcomes after cancer surgery. The investigators hypothesize that use of epidural anesthesia-analgesia may improve long-term survival in elderly patients after major surgery for cancer.

Conditions

  • Elderly
  • Malignant Tumor
  • Surgical Resection
  • Epidural Anesthesia
  • Long-term Outcome

Interventions

DRUG

Combined epidural-general anesthesia

Combined epidural-general anesthesia and postoperative epidural analgesia. General anesthesia is performed as that in the general anesthesia group. Epidural anesthesia is performed with ropivacaine. Epidural analgesia is performed with a mixture of ropivacaine and sufentanil.

DRUG

General anesthesia

General anesthesia and postoperative intravenous analgesia. General anesthesia is performed with propofol induction and propofol and/or sevoflurane maintenance. Intravenous analgesia is performed with morphine.

Sponsors & Collaborators

  • Peking University People's Hospital

    collaborator OTHER
  • Peking University Third Hospital

    collaborator OTHER
  • Beijing Hospital

    collaborator OTHER_GOV
  • Beijing Shijitan Hospital, Capital Medical University

    collaborator OTHER
  • Peking University

    collaborator OTHER
  • Peking University First Hospital

    lead OTHER

Principal Investigators

  • Dong-Xin Wang, MD · Peking University First Hospital

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
60 Years
Max Age
90 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2014-11-01
Primary Completion
2019-09-30
Completion
2019-09-30

Countries

  • China

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03012945 on ClinicalTrials.gov