Skip to content

The effect of ketamine combined with oxycodone in postoperative pain control in elderly patients undergoing abdominal surgery

The effect of ketamine combined with oxycodone in postoperative pain control in elderly patients undergoing abdominal surgery

Status
Recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500100472
Enrollment
Unknown
Registered
2025-04-10
Start date
2025-04-10
Completion date
Unknown
Last updated
2025-04-14

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

Conditions

Abdominal Surgery in the Elderly

Interventions

Ketamine combined with oxycodone combination group(Group SO):Intravenous injection of oxycodone injection is administered 30 minutes before the end of the surgery. Meanwhile, esketamine is intravenous
Oxycodone group (C):Administer Oxycodone Hydrochloride Injection 30 minutes before the end of the surgery. At the same time, intravenously pump an equal dose of normal saline as that of esketamine. Af

Sponsors

Tianjin First Central Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
60 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. The operation time is more than 2 hours; 2. 65 years old<= age <= 80 years old; 3: ASA I-III; 4: BMI<30;

Exclusion criteria

Exclusion criteria: 1: Chronic cardiovascular or respiratory diseases; 2: Combined with severe organic or metabolic diseases such as liver and kidney; 3: Surgical contraindications or allergies to anesthetic drugs; 4: Long-term history of chronic pain, long-term use of analgesics, long-term drug abuse and alcoholism; 5: Language barriers, or patients who are unable to use PCA (intellectual disability, disorientation, Alzheimer's disease, etc.); 6: Weight less than 40kg; 7: History of Schizophrenia,epilepsy or myasthenia gravis; 8: Combined with hyperthyroidism or pheochromocytoma; 9: Other conditions deemed unsuitable for participation in the study;

Design outcomes

Primary

MeasureTime frame
Incidence of moderate to severe pain within 72 hours postoperatively (NRS>=4);

Secondary

MeasureTime frame
Pain intensity;Sleep quality;Agitation score (RS score);Sedation score (Ramsay score);

Countries

China

Contacts

Public ContactYing Sun

Tianjin First Central Hospital

sunying2771@163.com+86 136 2202 1052

Outcome results

None listed

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