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A randomized controlled study of intravenous combined with local application of cortisol hormones to promote early rehabilitation after total hip arthroplasty

A randomized controlled study of intravenous combined with local application of cortisol hormones to promote early rehabilitation after total hip arthroplasty

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100044745
Enrollment
Unknown
Registered
2021-03-26
Start date
2021-04-06
Completion date
Unknown
Last updated
2021-10-26

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

Conditions

End stage hip disease

Interventions

Intravenous dexamethasone group:intravenous dexamethasone 10 mg before surgery
Intravenous combined with topical dexamethasone group:intravenous and topical dexamethasone

Sponsors

West China Hospital of Sichuan University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1.Patients requiring primary total hip arthroplasty due to severe hip osteoarthritis, femoral head necrosis, and secondary osteoarthritis due to developmental hip dysplasia; 2.Aged between 20 and 80 years; 3.Body mass index is between 20 and 35 kg/m2; 4.The American Society of Anesthesiologists (American Society of Anesthesiologists, ASA) classification (anesthesia risk assessment) I to III level.

Exclusion criteria

Exclusion criteria: 1.Simultaneous operation of both hip joints; 2.Patients with blood diseases, diabetes, malignant tumors and abnormal coagulation function; 3.Patients with a history of myocardial infarction, cerebral infarction, pulmonary embolism and other thrombosis; 4.Those who received anticoagulant therapy within 6 months before operation; 5.Persons with severe hip malformation and previous history of hip surgery; 6.Persons allergic to narcotic drugs and sulfanilamide; 7.Alcoholism or long-term use of opioids; 8.Language impairment and inability to complete Visual analogue Scale (VAS); 9.Surgical limb neuropathy; 10.Mentally ill; 11.Patients with digestive tract ulcer.

Design outcomes

Primary

MeasureTime frame
Postoperative dosage of remedial morphine hydrochloride;VAS pain score;hip range of motion;inflammatory indicators;

Secondary

MeasureTime frame
nausea and vomiting;blood routine examination;Harris hip score;

Countries

China

Contacts

Public ContactKang Pengde

Department of Orthopaedics Surgery, West China Hospital of Sichuan University

kangpd@163.com+86 18280213153

Outcome results

None listed

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