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Less opioid anesthesia with esketamine in combination with dexmedetomidine in gynecological laparoscopic surgery

Less opioid anesthesia with esketamine in combination with dexmedetomidine in gynecological laparoscopic surgery

Status
Recruiting
Phases
Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500096491
Enrollment
Unknown
Registered
2025-01-24
Start date
2025-03-01
Completion date
Unknown
Last updated
2025-01-27

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

Conditions

gynecology department

Interventions

Control group:Use of opioids
LOA group:Use esketamine and dexmedetomidine in combination with sufentanil

Sponsors

The First People's Hospital Lianyungang
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 60 Years

Inclusion criteria

Inclusion criteria: 1. Patients undergoing elective endoscopic gynecological surgery. 2. American Association of Anesthesiologists (ASA) Patient Grade I to II. 3. Age 20-60 years old. 4. Patients were informed of the main test methods and possible adverse reactions, and signed informed consent. 5. Heart, lung, liver, kidney and coagulation function were not abnormal. 6. The patient requested the use of a self-controlled analgesic device after surgery.

Exclusion criteria

Exclusion criteria: 1, ASA? level or above; 2. A history of allergy to or contraindication to ropivacaine, esketamine, or nonsteroidal anti-inflammatory drugs (NSAID) (serious risk of elevated blood pressure and intracranial pressure, poorly controlled or untreated hypertension, untreated or undertreated hyperthyroidism, gastrointestinal bleeding); 3, have mental illness and other chronic pain or other conditions that may confuse the analgesic response; 4, can not read and write Chinese, communication barriers; 5. Patients with severe heart disease and respiratory disease; 6. Patients with serious skin damage and infection in the ultrasound scan area; 7. Reluctance to use intravenous pain relief pumps and refusal to participate

Design outcomes

Primary

MeasureTime frame
Quality of Recovery-40;

Secondary

MeasureTime frame
Visual analogue scale (VAS) scores;heart rate ;Use of sufentanil;The number of effective compressions of the analgesic pump;Incidence of bradycardia;Incidence of nausea and vomiting;Incidence of dizziness;Incidence of increased oral secretions;Incidence of respiratory depression;

Countries

China

Contacts

Public ContactHao Conghui

The First People's Hospital Lianyungang

haoconghui2022@163.com+86 189 6132 5080

Outcome results

None listed

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