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Effect of propofol combined with opioid intravenous anesthesia on euphoric response in patients undergoing painless gastrointestinal endoscopy

Effect of propofol combined with opioid intravenous anesthesia on euphoric response in patients undergoing painless gastrointestinal endoscopy

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500096595
Enrollment
Unknown
Registered
2025-01-26
Start date
2025-02-15
Completion date
Unknown
Last updated
2025-02-03

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

Conditions

Addiction to drugs

Interventions

Control group:Propofol + normal saline
Fentanyl group:Propofol and fentanyl
Nalbuphine group:Propofol + nalbuphine

Sponsors

Suzhou Xiangcheng People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Age 18 to 75 years old; 2. Body mass index (BMI) 18.5 to 30 kg/m^2; 3. ASA classification I to III; 4. Mallampati classification I to III; 5. Patients undergoing painless gastroscopy and colonoscopy procedures; 6. Patients who can understand the entire clinical research process and sign an informed consent form.

Exclusion criteria

Exclusion criteria: 1. Patients with severe heart, lung, and brain diseases; 2. Patients with severe obstructive sleep apnea syndrome; 3. Patients with severe esophageal or gastrointestinal motility disorders; 4. Patients who have been taking opioids or sedatives for a long time and show a clear dependence on sedation or analgesia; 5. Patients who are allergic to propofol, fat emulsion, soy or egg products; 6. Pregnant women or women who are breastfeeding; 7. Patients with language communication disorders, who are unable to cooperate or have mental health disorders; 8. Patients with Mallampati classification IV, mouth opening <2.5cm; who are predicted to have or have had difficulty with the airway or have an abnormal history of surgical anesthesia recovery; 9. Long-term alcoholics.

Design outcomes

Primary

MeasureTime frame
Center for the Study of Addictions-Morphine-Amphetamine subscale (MBG);

Secondary

MeasureTime frame
Center for Addiction Research Scale (ARCI) total score;Center for Addiction Research Scale - pentobarbital, chlorpromazine, Alcohol subscale (PCAG) score;Center for Addiction Research Scale (LSD) score;Pittsburgh Sleep Quality Index (PSQI);Dreams: No dreams, good dreams (pleasant, positive), nightmares (unpleasant, negative);Surgical Volume Index (SPI);Time to recovery;Time awake;Time of induction;Satisfaction: (VAS score 0-10, endoscopists);Center for the Study of Addictions-Morphine-Amphetamine subscale (MBG);

Countries

China

Contacts

Public ContactLi Yan;Ma Chuntao

Suzhou Xiangcheng People's Hospital

szxcliyan@sina.com+86 137 7182 9585

Outcome results

None listed

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