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Ultrasound-based study of gastric motility patterns and characteristics in patients with disorders of consciousness

Ultrasound-based study of gastric motility patterns and characteristics in patients with disorders of consciousness

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2400094343
Enrollment
Unknown
Registered
2024-12-20
Start date
2024-12-30
Completion date
Unknown
Last updated
2025-01-06

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

Conditions

Disorders of consciousness

Interventions

Consciousness impairment group:None
Healthy control group:None

Sponsors

Shenzhen Second People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: Consciousness impairment group: 1. DOC caused by various brain injury diseases that meet the diagnostic criteria for vegetative state (loss of cognitive ability, no conscious activity, inability to execute commands, ability to open eyes automatically or under stimulation, sleep-wake cycle, inability to comprehend and express language, maintenance of basic vital signs such as respiration, blood pressure, etc., and preservation of basic functions of the subthalamus and the brainstem) and diagnostic criteria for minimally conscious state (executing simple commands, making gestures or responding whether accurately or not, understanding and expressing language, and responding to actions and emotions appropriate to the external environment); patients who Patients with the diagnostic criteria of minimal consciousness (can understand and express language and respond to the external environment by making simple commands, gestures, or yes/no answers, regardless of whether they are accurate or inaccurate, and can respond to the external environment with appropriate actions and emotions); 2.This is the first episode of the disease; 3. Age >= 18 years; 4.Have not used drugs that affect gastrointestinal motility 3 days before the trial; 5.Agreed to sign the informed consent form for this clinical study. Healthy control group: 1. Physically and mentally healthy, without chronic diseases; 2. Age >= 18 years old.

Exclusion criteria

Exclusion criteria: Consciousness impairment group: 1. Combined gastrointestinal obstruction, bleeding, gastrointestinal surgery, malignant tumours and other severe gastrointestinal impairment; 2. Pregnant women and patients after caesarean section; 3. People with severe organ dysfunction; 4. Combined with severe abdominal distension, obesity, abdominal wall deformities and other inability to perform abdominal ultrasonography; 5. Patients with incomplete medical records, who are unable to carry out data collection. Healthy control group: 1.Within one week, there are digestive symptoms such as nausea, vomiting, acid reflux, etc; 2. Those who have taken medication or health supplements within one month; 3. Pregnant women and cesarean section, the latter; 4. Individuals with gastrointestinal diseases or a history of surgery or abdominal surgery.

Design outcomes

Primary

MeasureTime frame
Gastric emptying rate ;Motility index;

Secondary

MeasureTime frame
Nutritional status;Complication;Risk of aspiration;

Countries

China

Contacts

Public ContactWang Yulong

Shenzhen Second People's Hospital

345399075@qq.com+86 755 8336 6388

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026