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A prospective cohort study on the postoperative analgesic effect and rehabilitation quality of elderly patients undergoing hip replacement surgery using hydromorphone combined with hip capsule blockade

A prospective cohort study on the postoperative analgesic effect and rehabilitation quality of elderly patients undergoing hip replacement surgery using hydromorphone combined with hip capsule blockade

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600118796
Enrollment
Unknown
Registered
2026-02-11
Start date
2026-02-28
Completion date
Unknown
Last updated
2026-02-16

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

Conditions

Postoperative analgesia for elderly patients undergoing hip replacement surgery

Interventions

Group A (exposure group):The PCA pump drug used in Group A is hydromorphone. The formula is hydromorphone 0.2mg/kg+ondansetron 16mg+physiological saline diluted to 100ml. Parameters: background dose 2
Group B (control group):Group B used PCA pump drug sufentanil. Formula: Sufentanil 2 µ g/kg+ondansetron 16mg+diluted with physiological saline to 100ml. Parameters: background dose 2ml/h, single compr

Sponsors

Ningjin County People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
65 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Age = 65 years old; 2. American Society of Anesthesiologists classification I-III; 3. Planned elective unilateral primary total hip replacement surgery; 4. Voluntarily participate and sign a written informed consent form.

Exclusion criteria

Exclusion criteria: 1. Known allergy to opioids (hydromorphone, sufentanil) or contraindications to their use; 2. Severe liver or kidney dysfunction; 3. Long-term chronic use of opioids or history of substance abuse; 4. Severe cognitive impairment, mental illness, or inability to communicate, making pain assessment impossible; 5. Surgical site infection or coexisting neurological disorders affecting functional assessment; 6. Intraoperative switch to other analgesic regimens or occurrence of serious complications.

Design outcomes

Primary

MeasureTime frame
Rest and activity VAS scores at 6h, 12h, 24h, and 48h postoperatively;

Secondary

MeasureTime frame
Total opioid dosage within 48 hours after surgery;PCA compression frequency (effective compression/total compression);First time getting out of bed;Harris hip score at 1 week/1 month/3 months after surgery;length of hospital stay;

Countries

China

Contacts

Public ContactYali Wang

Ningjin County People's Hospital

541615088@qq.com+86 158 5346 9974

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 19, 2026