Skip to content

Determining the optimal dose of oliceridine combined with propofol during day-surgery hysteroscopy

Determining the optimal dose of oliceridine combined with propofol during day-surgery hysteroscopy

Status
Recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500101669
Enrollment
Unknown
Registered
2025-04-28
Start date
2025-03-03
Completion date
Unknown
Last updated
2025-05-05

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

Conditions

Hysteroscopic surgery

Interventions

0.015mg/kg group:0.015mg/kg Oliceridine
0.025mg/kg group:0.025mg/kg Oliceridine
0.02mg/kg group:0.02mg/kg Oliceridine
0.01mg/kg group:0.01mg/kg Oliceridine
0.03mg/kg group:0.03mg/kg Oliceridine

Sponsors

Zhejiang Xiaoshan Hospital
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 55 Years

Inclusion criteria

Inclusion criteria: 1. Patients scheduled for hysteroscopy requiring intravenous anesthesia; 2. American Society of Anesthesiologists (ASA) physical status I or II; 3. Aged 18 to 55 years; 4. Body mass index (BMI) between 18 and 25 kg/m^2;

Exclusion criteria

Exclusion criteria: 1. History of cardiopulmonary diseases,including ECG abnormalities (QTc interval of >470 milliseconds ); 2. Women who were pregnant or breastfeeding; 3. Hepatic and renal dysfunction; 4. Obstructive sleep apnea-hypopnea syndrome(OSAHS); 5. Use of agents that could affect analgesic response (central a-adrenergic agents, antiepileptics, neuroleptics, antidepressants, antipsychotics); 6. History of narcotics such as opioid and propofol hypersensitivity; 7. At risk of aspiration; 8. Difficulty with cervical dilatation, defined as dilatation lasting > 5 minutes;

Design outcomes

Primary

MeasureTime frame
Response rate in each dose group (0.01,0.015,0.02,0.025, or 0.03 mg·kg–1 group);

Secondary

MeasureTime frame
Time to anesthesia emergence;Intraoperative vital signs;Surgery duration;Visual analogue scale (Vas) pain score;Adverse reactions;Propofol requirements;

Countries

China

Contacts

Public ContactSong Congzhong

Zhejiang Xiaoshan Hospital

scz112@126.com+86 571 83865708

Outcome results

None listed

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