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Randomized controlled trial study on analgesic effect of oxycodone on visceral pain

Randomized controlled trial study on analgesic effect of oxycodone on visceral pain

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100052205
Enrollment
Unknown
Registered
2021-10-22
Start date
2021-11-01
Completion date
Unknown
Last updated
2022-06-27

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

Conditions

visceral pain

Interventions

Group 1:Flurbiprofen axel 50mg
Group 2:Oxycodone 0.12 mg/kg
Group 3:Oxycodone 0.12mg/kg + flurbiprofen axetil 50mg

Sponsors

The First Hospital of Shanxi Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. ASA classification I-II; 2. Aged 18-65 years; 3. Those who plan to undergo hysteroscopic treatment; 4. Understand clearly, participate in this subject voluntarily, and sign the informed consent.

Exclusion criteria

Exclusion criteria: 1. Patients with serious heart, lung, liver, kidney and hematopoietic system diseases; 2. Those with a history of alcoholism and smoking; 3. Patients with clinical mental and speech disorders and unable to cooperate with the examination; 4. Those with neuroendocrine system diseases; 5. Allergic constitution and allergic to NSAIDs and experimental drugs; 6. Preoperative pulmonary function test showed moderate or more obstructive pulmonary ventilation dysfunction.

Design outcomes

Primary

MeasureTime frame
Visceral pain;

Secondary

MeasureTime frame
Wake up indicators;Satisfaction;Adverse reactions;

Countries

China

Contacts

Public ContactTian Shouyuan

The First Hospital of Shanxi Medical University

chinatsyjj@126.com+86 13803401773

Outcome results

None listed

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