Skip to content

Effects of Intravenous Lidocaine Infusion on Acute and Chronic Pain After Orthopedic Trauma Surgery in Adult Patients

Effects of Intravenous Lidocaine Infusion on Acute and Chronic Pain After Orthopedic Trauma Surgery in Adult Patients

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600128606
Enrollment
Unknown
Registered
2026-07-22
Start date
2026-07-22
Completion date
Unknown
Last updated
2026-08-03

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

Conditions

Acute and chronic pain following surgery for trunk or limb fractures in adults

Interventions

group C:Intraoperative intravenous infusion of 0.9% normal saline .
group L:Intraoperative intravenous infusion of lidocaine

Sponsors

Yiling Hospital Of Yichang City
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Age: 18–65 years; 2. ASA classification II–III; 3. Patients requiring internal fixation due to limb fractures or spinal trauma and scheduled for surgical intervention at Yiling Hospital; 4. The patient or their legally authorized representative has signed an informed consent form.

Exclusion criteria

Exclusion criteria: 1. Patients with comorbid conditions that are not adequately controlled, such as hypertension, diabetes, chronic pain, epilepsy, asthma, renal impairment (BUN and/or Cr > twice the normal value), or hepatic impairment (ALT and/or AST > 1.5 times the normal value); 2. Patients with traumatic brain injury or severe visceral injuries—including visceral rupture, shock, or other critical conditions—as well as those with severe infections or sepsis; 3. Patients requiring emergency surgery, such as those with puncture wounds, blast injuries, gunshot wounds, or stab wounds; 4. Patients allergic to any component of anesthetic agents or with confirmed or suspected history of opioid abuse; 5. Patients undergoing surgery lasting less than 30 minutes or exceeding 180 minutes; 6. Patients who refuse, disagree with, or cannot comprehend the study protocol; 7. Patients with other conditions deemed unsuitable by investigators for inclusion.

Design outcomes

Primary

MeasureTime frame
First functional exercise session duration;postoperative pain scores;chronic pain scores;

Secondary

MeasureTime frame
Intraoperative opioids consumption;Postoperative nausea and vomiting;Time of first meal;Time required for intestinal ventilation to recover;Hemodynamic parameters (hypertension, hypotension, tachycardia, bradycardia);postoperative analgesic medications consumption;Post-anesthetic sedation score;

Countries

China

Contacts

Public ContactJiang Hongying

Yiling Hospital Of Yichang City

656639108@qq.com+86 717 7534158

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Aug 10, 2026