Effect of Scalp Nerve Block on the Recovery Quality of Parkinson's Patients After Deep Brain Stimulation

Naval Military Medical University

Status: Enrolling

Conditions: Parkinson Disease

Treatments: Other: scalp nerve block combined with intercostal nerve block using 0.5% ropivacaine

Study type: Interventional

Funder types: Other

Identifiers

NCT05353764

SNB-QoR

Details and patient eligibility

About

Patients diagnosed with Parkinson's disease (PD) undergoing deep Brain Stimulation (DBS) have a higher risk of perioperative complications and postoperative pain will affect quality of recovery (QoR) resulting in longer hospitalization time and higher hospital costs. Scalp nerve block (SNB) combined with intercostal nerve block (ICNB)can alleviate postoperative pain while effect of them on postoperative recovery quality of patients diagnosed with PD was unclear. Therefore, the investigators conducted a randomized controlled trails to provide a novel method for enhanced recovery and early prevention and treatment of acute pain after DBS surgery.

Enrollment: 88 estimated patients

Sex: All

Ages: 18 to 75 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• patients with PD who receive elective deep brain stimulation (DBS) surgery
• Aged ≥ 18
• American Society of Anesthesiologists (ASA) physical status of I-III
• Able to communicate normally

Exclusion criteria

• Allergy to local anesthetics
• Pre-existing infection at block site
• Severe coagulopathy
• Pre-existing neuropathic pain condition
• Previous history of DBS surgery
• unwilling to provide informed consent or poor compliance

Trial design

Primary purpose: Other

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Quadruple Blind

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88 participants in 2 patient groups

SNB group

Experimental group

Description:

patients in the SNB group will receive general anesthesia combined with scalp nerve block and intercostal nerve block with 0.5% ropivacaine.

Treatment:

Other: scalp nerve block combined with intercostal nerve block using 0.5% ropivacaine

control group

No Intervention group

Description:

patients in control group will receive general anesthesia without nerve block.