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Impact of Blocking the Glossopharyngeal Nerve on Gastroesophageal Reflux Disease

M

Muhammad

Status

Not yet enrolling

Conditions

Dysphagia

Treatments

Procedure: Injection
Behavioral: Rehabilitation therapy
Drug: Lidocaine

Study type

Interventional

Funder types

Other

Identifiers

NCT06304870
SYB-reflux

Details and patient eligibility

About

The goal of this clinical trial is to explore Clinical Effect of Glossopharyngeal Nerve Block on Pharyngeal Dysphagia Induced by Gastroesophageal Reflux Disease. The main question it aims to answer is:

• Can Glossopharyngeal Nerve Block improve dysphagia caused by gastroesophageal reflux symptoms on the basis of rehabilitation training? Participants will be randomly allocated into the control group or the experimental group, all under rehabilitation treatment, the experimental group will be given Glossopharyngeal Nerve Block once a day additionally. The study lasts 20 days for each participant. Researchers will compare the Rosenbek penetration-aspiration scale, Gastroesophageal Reflux Disease Questionnaire, Pressure pain threshold, to see if the Glossopharyngeal Nerve Block can help improve the symptom.

Full description

Gastroesophageal reflux is a common digestive disorder characterized by the backflow of stomach contents and fluids into the esophagus.

The goal of this clinical trial is to explore Clinical Effect of Glossopharyngeal Nerve Block on Pharyngeal Dysphagia Induced by Gastroesophageal Reflux Disease. The main question it aims to answer is:

• Can Glossopharyngeal Nerve Block improve dysphagia caused by gastroesophageal reflux symptoms on the basis of rehabilitation training? Participants will be randomly allocated into the control group or the experimental group, all under rehabilitation treatment, the experimental group will be given Glossopharyngeal Nerve Block once a day additionally. The study lasts 20 days for each participant. Researchers will compare the Rosenbek penetration-aspiration scale, Gastroesophageal Reflux Disease Questionnaire, Pressure pain threshold, to see if the Glossopharyngeal Nerve Block can help improve the symptom.

Enrollment

80 estimated patients

Sex

All

Ages

18 to 65 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Meeting the diagnostic criteria for Gastroesophageal Reflux Disease.
  • Age between 18 and 65 years.
  • Confirmed tongue-pharyngeal nerve injury by electromyography.
  • Esophageal manometry and barium swallow examination confirming the presence of pharyngeal dysphagia.
  • Normal higher brain function, able to cooperate with treatment.

Exclusion criteria

  • Brain vascular disease diagnosed.
  • Clinical assessment and swallowing videofluoroscopic examination revealing cognitive phase, oral preparatory phase, or oral phase disorders.
  • Concurrent presence of other neurological disorders such as Alzheimer's disease, traumatic brain injury, Parkinson's disease.
  • Esophageal obstruction and severe liver or kidney dysfunction
  • Subjective unwillingness to undergo the treatment and presence of psychiatric abnormalities, etc.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Quadruple Blind

80 participants in 2 patient groups, including a placebo group

Rehabilitation therapy+Placebo Glossopharyngeal Nerve Block
Placebo Comparator group
Description:
The study lasts 20d for each patient. During the treatment, All the participants are provided with the rehabilitation therapy and placebo nerve block.
Treatment:
Procedure: Injection
Behavioral: Rehabilitation therapy
Rehabilitation therapy+Glossopharyngeal Nerve Block
Experimental group
Description:
The study lasts 20d for each patient. During the treatment, All the participants are provided with the rehabilitation therapy. Based on this, the patients in the experimental group are provided with Stellate Ganglion Block , using 1.5ml of 2% Lidocaine hydrochloride (1ml: 0.5mg) and 500ug of Vitamin B12 (1ml: 0.5g), once a day.
Treatment:
Procedure: Injection
Behavioral: Rehabilitation therapy
Drug: Lidocaine

Trial contacts and locations

1

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Central trial contact

Lavie Ce, Master

Data sourced from clinicaltrials.gov

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