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Safety and efficacy of cocktail analgesic injection in pain management of patients with scoliosis undergoing posterior spinal fusion

Safety and efficacy of cocktail analgesic injection in pain management of patients with scoliosis undergoing posterior spinal fusion: A prospective randomized controlled study

Status
Recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-IPR-17013563
Enrollment
Unknown
Registered
2017-11-27
Start date
2017-12-01
Completion date
Unknown
Last updated
2017-12-11

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

Conditions

scoliosis

Interventions

Cocktail Group:cocktail analgesia
Control Group:normal saline+iv-PCA

Sponsors

Peking Union Medical College Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
12 Years to 21 Years

Inclusion criteria

Inclusion criteria: 1) Age between 12 to 21 years; 2) On the surgical waiting list for posterior spinal fusion surgeries at PUMCH due to scoliosis.Diagnosed with scoliosis; 4) American Society of Anesthesiologists (ASA) physical status I~II; 5) Understand and comply with the study protocol.

Exclusion criteria

Exclusion criteria: 1) History of hypersensitivity to ropivacaine, diprospan, fentanyl or sulfonamide; 2) Serious allergic reaction to any other drugs; 3) Coagulation dysfunction; 4) Severe hepatic, renal, or cardiovascular dysfunction; 5) Revision surgery or growing rod lengthening surgery; 6) Inability to provide informed consent due to mental incompetence (e.g., intellectual disability, dementia); 7) Drug or alcohol abuse; 8) Limited Chinese language fluency.

Design outcomes

Primary

MeasureTime frame
visual analog scale pain score.;

Secondary

MeasureTime frame
Sufentanil consumption;Time to first use of IV-PCA;Rescue analgesia consumption;

Countries

China

Contacts

Public ContactShugang Li

Peking Union Medical College Hospital

lishugangpumc@163.com+86 18311073793

Outcome results

None listed

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