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Effect of esketamine combined with sufentanil on postoperative pain in patients with stomatology

Effect of esketamine combined with sufentanil on postoperative pain in patients with stomatology

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400086662
Enrollment
Unknown
Registered
2024-07-08
Start date
2023-11-16
Completion date
Unknown
Last updated
2024-07-15

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

Conditions

Impacted tooth, jaw fracture

Interventions

Esketamine combined with sufentanil group:Esketamine combined with sufentanil is used for intravenous patient-controlled analgesia pump, with the formula of the analgesia pump being sufentanil 1.5µg/k
Sufentanil group:Sufentanil is used for intravenous patient-controlled analgesia pump, with the formula of the analgesia pump being sufentanil 2µg/kg plus palonosetron 0.5mg, diluted to 100ml with nor

Sponsors

First People's Hospital of Lianyungang
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Patient age between 18 to 75 years old; 2. Patients scheduled for elective oral surgery; 3. BMI between 18 to 30 kg/m²; 4. ASA I to III; 5. Fully understand and voluntarily participate in this study, and have signed the informed consent form.

Exclusion criteria

Exclusion criteria: 1. Allergic to the experimental drug; 2. Patients with unstable ischemic heart disease, severe pulmonary hypertension, poorly controlled or untreated hypertension; 3. At serious risk of increased intracranial or intraocular pressure; 4. A history of untreated or undertreated hyperthyroidism or epilepsy; 5. Long-term use of non-steroidal anti-inflammatory drugs, opioids, sedatives; 6. Any history or treatment of neurological or psychiatric disorders, including substance abuse, anxiety, or depression; 7. Vital organ dysfunction, liver dysfunction, renal dysfunction; 8. Those who do not agree or are unable to use intravenous patient-controlled analgesia (PCIA) pumps.

Design outcomes

Primary

MeasureTime frame
VAS pain score;

Secondary

MeasureTime frame
Ramsay sedation score;QoR-15 score;Incidence of Drug-Related Adverse Reactions;The Use of Sufentanil within 48 Hours Post-Surgery;Pain Relief Satisfaction Score;

Countries

China

Contacts

Public ContactYing Chen

First People's Hospital of Lianyungang

jshlyg@sina.cn+86 189 6132 2003

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 6, 2026