Randomized Controlled Study of Optical 3D Navigated Repetitive Transcranial Magnetic Stimulation for Achalasia.
Esophageal Achalasia, Transcranial Magnetic Stimulation, Repetitive, Vagus Nerve Motor Disorder
About this trial
This is an interventional treatment trial for Esophageal Achalasia focused on measuring Achalasia, rTMS, fMRI, Non-invasive
Eligibility Criteria
Inclusion Criteria: Aged more than 18 years old, less than 75 years old; Clinical symptoms evaluation, HREM, esophageal barium meal examination confirmed the diagnosis of achalasia; Willing to sign informed consent. Exclusion Criteria: Presence of metal hardware in close contact with the discharge coil (e.g., cochlear implant, internal pulse generator, or drug pump). Note: Cochlear implants include electrodes, magnets, loop antennas, and electronic chips under the scalp implanted in the cochlea; Intracranial metal implants; Patients with cardiac pacemakers, vagal nerve stimulation (VNS) systems, spinal cord stimulators, and deep brain stimulation implanted with pulse generators should be used with caution; People at higher risk of noisy hearing loss and patients with hypoacusis symptoms should be used with caution; Pregnancy; Severe or recent heart disease; Personal history of epilepsy, use of known drugs that lower the seizure threshold, and other factors that may lower the seizure threshold (e.g., lack of sleep, infection, and alcohol abuse); Increased intracranial pressure; Acute phase of intracranial infection and hemorrhagic disease; Contraindications to MRI examination or claustrophobia; Refusal to sign informed consent.
Sites / Locations
- Nanjing Drum Tower Hospital
Arms of the Study
Arm 1
Arm 2
Sham Comparator
Experimental
Sham group
rTMS group
Intervention Name and Specification: Placebo coil (Magstim Company, Whitland, UK): looks and sounds consistent with true coil but does not produce current stimulation.
5Hz-rTMS group 10Hz-rTMS group 30Hz-rTMS group Intervention Name and Specification: Transcranial magnetic stimulator (M-100 Ultimate, Yingzhi Technology Co., Ltd., China) 70 mm diameter figure-of-eight coil (BY90A, Yingzhi Technology Co., Ltd., China). Each group received acute and chronic stimulation, respectively. In the acute stimulation stage, patients only needed to do rTMS once, and HREM and HRV were administered before and after rTMS; in the chronic stimulation stage, patients received 25 minutes of rTMS true stimulation each time a day for 20 times, which was completed within 30 days, and the true stimulation parameters were the same as those of acute stimulation.