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The Impact of Anti-inflammatory with Methylprednisolone Before Surgery or Parecoxib Sodium After Surgery on Postoperative Analgesia in Hysterectomy with Oxycodone Analgesia

The Impact of Anti-inflammatory with Methylprednisolone Before Surgery or Parecoxib Sodium After Surgery on Postoperative Analgesia in Hysterectomy with Oxycodone Analgesia

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-IOR-16009152
Enrollment
Unknown
Registered
2016-09-04
Start date
2016-09-05
Completion date
Unknown
Last updated
2017-11-20

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

Conditions

Hysteromyoma,Adenomyosis

Interventions

Group M:Methylprednisolone before surgery
Group P:Parecoxib Sodium after surgery
Group O:No measure of anti-inflammatory

Sponsors

Xuanwu Hospital of CCMU
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. American Society of Anesthesiologists (ASA) physical status I~II; 2. Aged 18~65 years; 3. Patients scheduled for laparoscopic assisted vaginal hysterectomy in Xuanwu Hospital.;Inclusion criteria: 1. American Society of Anesthesiologists (ASA) physical status I~II; 2. Aged 18~65 years; 3. Patients scheduled for laparoscopic assisted vaginal hysterectomy in Xuanwu Hospital.

Exclusion criteria

Exclusion criteria: 1. The patient's too old or too young, ASA physical status =III; 2. Significant renal impairment(creatinine>177µmol/L); Congestive heart-failure (NYHA status IV) or other severe systemic disease; 3. Cerebral vascular disease within 6 months, include cerebral hemorrhage and infraction, or over 6 months but with neurological sequelae; 4. Patients with severe malnourishment or deficiency of hormone secretion; 5. Patients with smoking history; 6. Acute trauma or inflammatory disease; 7. Patients with diseases which would lead to high infalmmatory factors, such as infection, cancer etc.; 8. History of drug and alcohol abuse; 9. Patients with contraindication of using parecoxib sodium, methylprednisolone or oxycodone; 10. Patients who disagree to participate in the research.;Exclusion criteria: 1. The patient's too old or too young, ASA physical status =III; 2. Significant renal impairment(creatinine>177µmol/L); Congestive heart-failure (NYHA status IV) or other severe systemic disease; 3. Cerebral vascular disease within 6 months, include cerebral hemorrhage and infraction, or over 6 months but with neurological sequelae; 4. Patients with severe malnourishment or deficiency of hormone secretion; 5. Patients with smoking history; 6. Acute trauma or inflammatory disease; 7. Patients with diseases which would lead to high infalmmatory factors, such as infection, cancer etc.; 8. History of drug and alcohol abuse; 9. Patients with contraindication of using parecoxib sodium, methylprednisolone or oxycodone; 10. Patients who disagree to participate in the research.

Design outcomes

Primary

MeasureTime frame
NRS score;Duration of postoperative pain;;NRS score;Duration of postoperative pain;

Secondary

MeasureTime frame
TNF-a;C reactive protein;;TNF-a;C reactive protein;

Countries

China

Contacts

Public ContactWANG TIANLONG;WANG TIANLONG ;

Xuanwu Hospital of CCMU;Xuanwu Hospital of CCMU

w_tl5595@hotmail.com;w_tl5595@hotmail.com+86 13910525304;+86 13910525304

Outcome results

None listed

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