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Tizanidine and celecoxib combination vs. alone on opioid use, pain, and postoperative recovery after hip fracture surgery Effects of tizanidine and celecoxib in combination versus alone on postoperative opioid use, pain, and postoperative recovery after hip fracture: a prospective, double-blind, randomized controlled trial

Tizanidine and celecoxib combination vs. alone on opioid use, pain, and postoperative recovery after hip fracture surgery Effects of tizanidine and celecoxib in combination versus alone on postoperative opioid use, pain, and postoperative recovery after hip fracture: a prospective, double-blind, randomized controlled trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500100850
Enrollment
Unknown
Registered
2025-04-16
Start date
2025-04-17
Completion date
Unknown
Last updated
2025-04-21

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

Conditions

Hip Fracture

Interventions

Tizanidine + celecoxib group:Oral tizanidine 6 mg 1 hour preoperatively and orally for 7 consecutive days (celecoxib 200 mg twice daily
oral tizanidine 4 mg three times daily).
Celecoxib group:Oral (6 mg placebo) 1 hour preoperatively and orally for 7 consecutive days (celecoxib 200 mg twice daily
oral placebo 4 mg three times daily)

Sponsors

Affiliated Hospital of North Sichuan Medical College
Lead Sponsor

Eligibility

Sex/Gender
All
Age
65 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. The diagnostic criteria are consistent with "Practical Orthopedics"; 2. Meet the relevant indications for surgery and anesthesia; 3. American Society of Anesthesiologists (ASA) anesthesia classification is grade II.~III.; 4. Age>=65 years; 5. First unilateral hip fracture with fresh closed fracture; 6. Received intramedullary nail or hollow screw and FNS treatment of proximal femoral anti-rotation screw; 7. Patients who are willing to participate and have signed the informed consent form.

Exclusion criteria

Exclusion criteria: 1. Multiple fractures or open fractures, non-osteoporotic pathological fractures; 2. Patients with severe heart, lung and other vital organ diseases; 3. Those who are inactive or bedridden for a long time before injury or have neurological deficits, primary pain-causing diseases or pain intolerance; 4. Those with severe Alzheimer's disease or mental illness or who are unable to cooperate or do not cooperate; 5. History of active peptic ulcer or bleeding within 6 months; 6. Those who take relevant analgesic drugs or are allergic to non-steroidal anti-inflammatory drugs (NSAIDs) or are dependent on analgesic and anesthetic drugs before admission; 7. Those who are allergic to drugs related to this study

Design outcomes

Primary

MeasureTime frame
Postoperative diazoxide consumption;Postoperative tramadol consumption;Pain scores;

Secondary

MeasureTime frame
Sleep quality;Transferase level (enzyme);Time to first analgesic resuscitation;Length of postoperative hospitalization;

Countries

China

Contacts

Public ContactLuo Yue

Affiliated Hospital of North Sichuan Medical College

760455936@qq.com+86 183 0831 2835

Outcome results

None listed

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