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Effect of Intravenous Lidocaine on Serum miRNA-135a in Patients Undergoing Non-cardiac Surgery

Effects of Intravenous Lidocaine on Serum miRNA-135a and Its Downstream Proteins Rock2 and Add1 in Elderly Patients Undergoing Non-cardiac Surgery Under General Anesthesia.

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05503043
Enrollment
50
Registered
2022-08-16
Start date
2022-09-01
Completion date
2023-12-30
Last updated
2022-08-16

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

Conditions

Organ Protection

Keywords

lidocaine, postoperative cognitive dysfunction, miRNA-135a, Rock2, Add1

Brief summary

The purpose of this study is to investigate the effects of intravenous lidocaine on serum miRNA-135a and its downstream proteins Rock2 and Add1 in elderly patients undergoing non-cardiac under general anesthesia.

Detailed description

Postoperative cognitive dysfunction (POCD) is a major complication following surgeries and anesthesia, especially in elderly individuals. Lidocaine, an inexpensive, widely available, and relatively safe compound, is a local anesthetic that readily crosses the blood-brain barrier. Intravenous lidocaine can reduce the incidence of POCD. However, the mechanism is still unclear. Rock2 and Add1, which are regulated by miRNA-135a, play a key role in learning, memory, and cognition. The objective of this study is to investigate the efficacy of intravenous lidocaine on the incidence of early POCD, and the levels of Rock2, Add1, and miRNA-135a in elderly patients undergoing non-cardiac under general anesthesia.

Interventions

DRUGLidocaine

Intravenous bolus of 1.5 mg/kg of lidocaine followed by a continuous infusion of 3.0 mg/kg for the frst hour, 1.5 mg/kg for the second hour, 0.7 mg/kg until the end of the surgery.

DRUGNormal saline

Patients are received equal volumes of saline intravenously until the end of the surgery

Sponsors

General Hospital of Ningxia Medical University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
DOUBLE (Subject, Caregiver)

Eligibility

Sex/Gender
ALL
Age
65 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

* Patients undergoing elective non-cardiac surgery under general anesthesia * ASA physical status II-III * Aged ≥65 years

Exclusion criteria

* Serious heart, lung, liver and kidney diseases * Central nervous system injury * Mental illness and drug dependence * On regular use of analgesic/sedative/antidepressant * Unable to cooperate * Allergy to lidocaine * MMSE \< 23 points

Design outcomes

Primary

MeasureTime frameDescription
Changes from Baseline miRNA-135A at the end of surgery immediately and 1, 3days after surgeryat preoperation, at the end of surgery immediately, 1day and 3day after surgeryVenous blood was extracted, and the serum miRNA-135a level of patients were detected by PCR and ELISA before surgery, at the end of surgery, 1day and 3day after surgery
Changes from Baseline Rock2 at the end of surgery immediately and 1, 3days after surgeryat preoperation, at the end of surgery immediately, 1day and 3day after surgeryVenous blood was extracted, and the serum Rock2 level of patients were detected by PCR and ELISA before surgery, at the end of surgery, 1day and 3day after surgery
Changes from Baseline Add1 at the end of surgery immediately and 1, 3days after surgeryat preoperation, at the end of surgery immediately, 1day and 3day after surgeryVenous blood was extracted, and the serum Add1 level of patients were detected by PCR and ELISA before surgery, at the end of surgery, 1day and 3day after surgery

Secondary

MeasureTime frameDescription
Changes from Baseline mini-mental state examination (MMSE) at the end of surgery immediately and 1, 3days after surgeryat preoperation,1day and 3day after surgeryMMSE was performed

Other

MeasureTime frameDescription
Postoperative cognitive dysfunction (POCD)at preoperation,1day and 3day after surgerythe incidence of POCD

Contacts

Primary ContactHanxiang Ma
mahanxiang@hotmail.com+86-13519591508
Backup ContactLi Zhao
zhaoli295@163.com+86-15595293568

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026