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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT04922359
Other study ID # 2021PHB059-001
Secondary ID
Status Not yet recruiting
Phase N/A
First received
Last updated
Start date June 1, 2021
Est. completion date May 15, 2023

Study information

Verified date May 2021
Source Peking University People's Hospital
Contact Jie Gu, attending
Phone 15210886376
Email hmugujie@163.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Spinal surgery often involves multiple segments. The trauma of surgery is large, the duration of postoperative pain is long, and the pain is severe. Therefore, the use of opioids in perioperative period is large. Although the application of * large amounts of opioids can effectively inhibit pain, it will delay the recovery of urine retention, sedation, respiratory depression and gastrointestinal function. The delayed recovery of gastrointestinal function will increase the postoperative complications, and then increase the length of hospital stay and the cost of patients. Therefore, reducing the dosage of opioids to promote the recovery of gastrointestinal function has become the research direction. Intravenous lidocaine has been proved to be effective in reducing the dosage of opioids during the perioperative period of gastrointestinal surgery and promoting the recovery of postoperative gastrointestinal function. However, there are few studies on the application of lidocaine during the perioperative period of spinal surgery, especially the impact on postoperative gastrointestinal function. In this study, a multicenter, randomized, double-blind, controlled study was conducted to explore the effect of perioperative lidocaine on the recovery of gastrointestinal function after adult lumbar surgery. We hypothesized that lidocaine could shorten the recovery time of gastrointestinal function after lumbar surgery


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 96
Est. completion date May 15, 2023
Est. primary completion date October 30, 2022
Accepts healthy volunteers No
Gender All
Age group 60 Years to 80 Years
Eligibility Inclusion Criteria: 1. age 60 to 80; 2. ASA physical status score of I, II or III; 3. Scheduled to undergo a posterior lumbar surgery; 4. Ideal body weight=80 kg; Exclusion Criteria: 1. Those who are refused to be included; 2. Those who are allergic to the drugs used in this study; 3. Emergency operation 4. Degree II or III atrioventricular block 5. heart failure 6. History of ALS, preexcitation or active dysrhythmia 7. Severe liver injury (bilirubin > 1.46 mg/dl) 8. Severe renal injury (creatinine clearance < 30 ml/min) or Renal failure 9. History of epilepsy 10. History of porphyria 11. Preoperative hypotension (SBP< 90mmHg) 12. Drug contraindications of NSAIDs 13. Allergic to anaesthetic

Study Design


Intervention

Drug:
Lidocain
Patients received 1.5mg/kg of intravenous lidocaine during induction of anesthesia and 1.5 mg/kg/h for anesthesia maintenance.
normal saline
Patients received 0.075ml/kg of intravenous normal saline during induction of anesthesia and 0.075ml/kg/h for anesthesia maintenance.

Locations

Country Name City State
China Peking University People's Hospital Beijing Beijing

Sponsors (3)

Lead Sponsor Collaborator
Peking University People's Hospital First Affiliated Hospital of Guangxi Medical University, Wangjing Hospital, China Academy of Chinese Medical Sciences

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary First anal exhaust time Time of first anal exhaust after operation Day 0
Secondary First defecation time Time of first defecation after operation Day 0
Secondary First diet time Time of first feeding after operation Day 0
Secondary Time to get out of bed Time to get out of bed after operation Day 0
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