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Research on strategies for improving the quality and safety of sedation and analgesia in digestive endoscopy

Research on strategies for improving the quality and safety of sedation and analgesia in digestive endoscopy

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500101278
Enrollment
Unknown
Registered
2025-04-23
Start date
2024-10-07
Completion date
Unknown
Last updated
2025-04-28

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

Conditions

Perioperative stress reaction, respiratory adverse events

Interventions

control group:Apply electroacupuncture patches to the same acupoints, but do not give electrical stimulation

Sponsors

Hebei General Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1.Patients undergoing gastroscopy with a GERD-Q score of 8 or higher. 2.The American Society of Anesthesiologists (ASA) classifies patients with grades I to III; 3.Aged between 18 and 80 years old; 4.Sign informed consent;

Exclusion criteria

Exclusion criteria: 1.Patients with an allergy to propofol. 2.Patients with severe arrhythmias, post-stent implantation, or pacemakers; 3.Patients with mental illness, who are unable to communicate verbally, or who take psychotropic medications orally for a long period of time; 4.Patients who refuse blood draws and patients who are averse to electrical stimulation; 5.Patients with acute upper gastrointestinal bleeding within 48 hours;

Design outcomes

Primary

MeasureTime frame
Perioperative adverse events;

Secondary

MeasureTime frame
cortisol;endorphin;The amount of oral secretions;Interleukin-4;C-reactive protein;

Countries

China

Contacts

Public ContactZhu Xichun

Hebei General Hospital

13703395257@163.com+86 311 85988255

Outcome results

None listed

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