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Clinical investigation of postoperative euphoria and perioperative mood changes and adverse events after painless gastroenteroscopy with ciprofol

Clinical investigation of postoperative euphoria and perioperative mood changes and adverse events after painless gastroenteroscopy with ciprofol

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500100981
Enrollment
Unknown
Registered
2025-04-17
Start date
2025-04-25
Completion date
Unknown
Last updated
2025-08-18

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

Conditions

mood changes

Interventions

Observation Group:Induction and maintenance of anesthesia using ciprofol

Sponsors

Northern Jiangsu People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. Proposed to perform painless GI endoscopy, and simple endoscopic maneuvers, such as single small polyp clamping, performing Hp tests, and so on; 2. Gender is not limited; 3. 18 years old <= age <= 70 years old; 4. ASA state: I-II; 5. 18kg/m^2< BMI <30 kg/m^2; 6. Informed consent, voluntary participation in the trial, and informed consent signed by the subjects themselves.

Exclusion criteria

Exclusion criteria: 1. Been adjudicated to have difficulty with respiratory management; 2. Participation in a clinical trial of another drug or device within 3 months prior to the Screening Period; 3. Subjects taking medications for psychiatric or neurological disorders (e.g., antidepressants, anxiolytics, convulsants, antiepileptics, etc.) or opioid analgesics, etc., for a variety of reasons (e.g., insomnia, pain, anxiety, etc.) within 3 months prior to the Screening Period; 4. Allergy or contraindication to the study drug or components thereof; 5. The subject has a severe communication impairment due to various reasons such as severe hearing deterioration; 6. Refusal to participate in this study; 7. Other subjects deemed unsuitable by the investigator.

Design outcomes

Secondary

MeasureTime frame
Fatigue condition;Short-term sleep in the 72h postoperative period;Perioperative adverse events;Subjects' satisfaction with the quality of anesthesia;Subjects' dreaming;Postoperative mobility;Pain level;level of emotion;

Primary

MeasureTime frame
Incidence and duration of euphoria;Changes in perioperative euphoria;Perioperative MBG score;

Countries

China

Contacts

Public ContactJu Gao

Northern Jiangsu People's Hospital Anesthesiology Department

doctor2227@163.com+86 180 5106 3988

Outcome results

None listed

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