Skip to content

The effects of pregabalin versus gabapentin combined with NSIADs on the pain of spinal surgery: a randomized controlled trial.

The effects of pregabalin versus gabapentin combined with NSIADs on the pain of spinal surgery

Status
Recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000035554
Enrollment
Unknown
Registered
2020-08-13
Start date
2020-08-12
Completion date
Unknown
Last updated
2020-08-17

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

Conditions

Degenerative diseases and injuries of the spine

Interventions

Group 1:Gabapentin combined with Celebrex
Group 2:Pregabalin and Celebrex
Group 3:Gabapentin combined with Parecoxib
Group 4:Pregabalin combined with Parecoxib

Sponsors

The First Affiliated Hospital of Chongqing Medical University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Subjects aged 18-85 years; 2. Single segment fusion and internal fixation: lumbar disc herniation, lumbar spinal stenosis, lumbar spondylolisthesis; 3. Two level fusion and internal fixation: lumbar disc herniation, lumbar spinal stenosis, lumbar spondylolisthesis; 4. Percutaneous vertebroplasty (PVP) and percutaneous kyphoplasty (PKP) for osteoporotic vertebral compression fractures.

Exclusion criteria

Exclusion criteria: 1. Patients allergic to amide local anesthetics or sulfonamides; 2. Patients with severe liver and kidney dysfunction, bronchospasm, asthma, active peptic ulcer and bleeding, severe heart failure, creatinine clearance rate < 60ml / min and creatinine greater than 110; 3. Pregnant women or objects in lactation period; 4. Patients with acute pancreatitis.

Design outcomes

Primary

MeasureTime frame
VAS scores;PCA dose;

Secondary

MeasureTime frame
time to ambulation;hospital stay;adverse events;

Countries

China

Contacts

Public ContactZhengxue Quan

The First Affiliated Hospital of Chongqing Medical University

quanzx18@126.com+86 13608321800

Outcome results

None listed

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