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Comparison of Anesthetic Effects of Dexmedetomidine Nasal Spray Combined with Propofol in Gastrointestinal Endoscopy

Comparison of Anesthetic Effects of Dexmedetomidine Nasal Spray Combined with Propofol in Gastrointestinal Endoscopy

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500109904
Enrollment
Unknown
Registered
2025-09-26
Start date
2025-10-01
Completion date
Unknown
Last updated
2025-09-29

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

Conditions

Gastrointestinal disease

Interventions

Dexmedetomidine nasal spray group:Dexmedetomidine Hydrochloride nasal spray was administered preoperatively
Saline solution group:0.9% sodium chloride nasal spray

Sponsors

The Second Affiliated Hospital of Xuzhou Medical University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Schedule a date for a painless gastrointestinal endoscopy; 2. The patient and family are informed and sign the informed consent form; 3. Age between 18-65 years, gender not limited; 4. ASA grade I-II; 5. No significant abnormalities in blood routine, electrocardiogram, and coagulation function results; 6. BMI controlled between 18-30 kg/m^2; no other serious comorbidities.

Exclusion criteria

Exclusion criteria: 1. Patients who are allergic to or contraindicated for the drugs relevant to this study; 2. Patients with significant impairment of important organ functions such as respiratory, circulatory, or liver and kidney function prior to surgery; 3. Patients with psychological issues or a history of mental illness; 4. Patients deemed to have difficult airway management; 5. Patients who have been taking anesthetics, analgesics, or sedatives long-term; 6. Patients with poorly controlled or untreated hypertension (resting blood pressure exceeding 180/100 mmHg); 7. Patients with severe cardiovascular history (e.g., unstable angina, heart failure, and arrhythmias); 8. Patients with hyperthyroidism; 9. Patients who refuse to participate in this study.

Design outcomes

Primary

MeasureTime frame
Respiratory depression;

Secondary

MeasureTime frame
Time to loss of consciousness (LOC);Recovery Time;hypotension;bradycardia;

Countries

China

Contacts

Public ContactXiaohui Wang

The Second Affiliated Hospital of Xuzhou Medical University

islawang615@163.com+86 157 2287 5979

Outcome results

None listed

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