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Effect of preoperative intervention in acute pain management group in elderly patients with hip fracture: a retrospective analysis

Effect of preoperative intervention in acute pain management group in elderly patients with hip fracture: a retrospective analysis

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500108343
Enrollment
Unknown
Registered
2025-08-28
Start date
2025-09-01
Completion date
Unknown
Last updated
2025-09-01

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

Conditions

Fracture of hip

Interventions

Ultrasound-guided fascial iliac space block intravenous self-controlled analgesia group (observation group):None
Intravenous self-controlled analgesia group (control group):None

Sponsors

Zhongda Hospital, Southeast University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
65 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Age>=65 years old, gender is not limited; 2. Patients receiving general anesthesia with ASA grade I~III; 3. Meet the diagnostic criteria for hip fracture through imaging examinations such as CT and X-ray and routine examination; 4. No history of anesthesia allergy; 5. All patients underwent hip fracture surgery for the first time; 6. No neurological diseases; 7. Use an intravenous analgesic pump during the perioperative period.

Exclusion criteria

Exclusion criteria: 1. Liver and kidney not within the normal range or combined with severe respiratory dysfunction (type I or II respiratory failure) before surgery; 2. Patients with severe mental illness or cognitive dysfunction; 3. Patients who have been taking opioids or antidepressants or sedatives for a long time; 4. Patients admitted to the ICU after surgery; 5. Severe allergic reactions during surgery, which are difficult to maintain hemodynamics; 6. After surgery, there was no single ultrasound-guided iliac fascial space block analgesia in the post-anesthesia recovery room.

Design outcomes

Primary

MeasureTime frame
Opioid consumption within 48 hours after surgery;

Secondary

MeasureTime frame
NRS pain score (at rest and when coughing);Pain scores and area under curve (AUC) in different postoperative time periods ;Cumulative opioid consumption in different postoperative time periods;Recovery time (the period from the end of the surgery to the removal of the tracheal tube);Time to first postoperative flatulence;Activities of daily living (Barthel Index,BI) score;Length of postoperative hospital stay;Incidence of postoperative nausea and vomiting (PONV);Postoperative delirium;Other related complications (pulmonary infection, skin itching, respiratory depression, drowsiness, etc.);

Countries

China

Contacts

Public ContactXie Jue

Zhongda Hospital, Southeast University

very_wang@126.com+86 180 1389 8998

Outcome results

None listed

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