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A randomized controlled study of the analgesia effect on lumbar spinal fusion surgery with low dose intrathecal morphine combined with patient-controlled intravenous anagesia

A randomized controlled study of the analgesia effect on lumbar spinal fusion surgery with low dose intrathecal morphine combined with patient-controlled intravenous anagesia

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1800016364
Enrollment
Unknown
Registered
2018-05-28
Start date
2018-06-01
Completion date
Unknown
Last updated
2018-06-05

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

Conditions

None

Interventions

ITM:intrathecal morphine injection
CON:None

Sponsors

Peking University Third Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: Patients undergoing low lumbar posterior decompression and fixation fusion surgery, ASA grade I, II, aged 18 to 80 years.

Exclusion criteria

Exclusion criteria: Patients Refusal, L2-3 has a herniated disc and neurological symptoms, have history of severe bronchial lung disease, sleep apnea, long-term application of opioid drugs, drug addiction, blood coagulation dysfunction, puncture infection, comprehension obstacles, inability to understand pain digital evaluation questionnaire), uncontrolled hypertension, diabetes, glaucoma and body mass index> 32.

Design outcomes

Primary

MeasureTime frame
Volume of postoperativesufentanil;—

Countries

China

Contacts

Public ContactXu Mao

Peking University Third Hospital

anae@163.com+86 13661380935

Outcome results

None listed

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