Safety and effectiveness of pregabalin in the management of postoperative pain in lumbar surgery

Status

Recruiting

Phases

Early Phase 1

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR2000028775

Enrollment

Unknown

Registered

2020-01-03

Start date

2020-02-01

Completion date

Unknown

Last updated

2020-01-06

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

Conditions

1. Lumbar disc herniation

Interventions

Pregabalin group: ?????????? ?????????? Postoperative analgesia with pregabalin

Celecoxib group: Postoperative analgesia with celecoxib

Eligibility

Sex/Gender

All

Age

18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. From February 1, 2020 to February 1, 2021 in our hospital, the patients were diagnosed as lumbar disc herniation or lumbar spinal stenosis or lumbar spondylolisthesis, and underwent posterior lumbar open surgery; 2. Those who voluntarily joined the study and signed the informed consent.

Exclusion criteria

Exclusion criteria: No

Design outcomes

Primary

Measure	Time frame
body mass index;Duration of disease;VAS score;JOA score;Hb;Alb;CRP;IL-6;TNF-a;Substance P;ß- endorphin;Postoperative incision drainage;Functional exercise time of lumbar dorsi muscle after operation;bed time;Length of Stay;	—

Countries

China

Contacts

Public ContactJie Hao

The First Affiliated Hospital of Chongqing Medical University

hjie2005@aliyun.com+86 13996120738

Outcome results

None listed

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