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The efficacy of parecoxib combined with paracetamol for reducing opioid consumption after breast cancer surgery: A prospective randomized controlled trial

The efficacy of intraoperative parecoxib with paracetamol for reducing opioid consumption in patient undergoing breast cancer surgery under general anesthesia: A prospective randomized controlled trial

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
TCTR
Registry ID
TCTR20230301004
Enrollment
60
Registered
2023-03-01
Start date
2021-08-01
Completion date
Unknown
Last updated
2026-08-03

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

Conditions

The efficacy of intra-operative parecoxib with paracetamol for reducing opioid consumption in patient undergoing breast cancer surgery under general anesthesia breast cancer surgery, parecoxib, paracetamol

Interventions

Parecoxib is an injectable parenteral prodrug of valdecoxib(selective COX-2 inhibitors), resulting in reduced production of prostaglandins, the substance that is involved in inflammation.4,5 Parecoxib
Active Comparator Drug,Placebo Comparator No treatment
Parecoxib combine with paracetamol intravenous,placebo( NSS)

Sponsors

FACULTY OF MEDICINE RESEARCH GRANT KHON KAEN UNIVERSITY
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: female age 18-65 year ASA classification 1-3 Patients scheduled for elective breast surgery under general anesthesia at operating room, Srinagarind hospital

Exclusion criteria

Exclusion criteria: Patients with hypersensitivity or contraindication to the study drugs. allergy for sulfamethoxazole History of opioid or steroid (Dexamethasone,Hydrocortisone) used. Pregnancy Psychologic problems Operation change Refuse to participate

Design outcomes

Primary

MeasureTime frame
Postoperative opioid consumption 24 hours measure opioid consumption (mg)

Secondary

MeasureTime frame
Post operative pain score 24 hour, 3 month numeric rating scale 0-10,assess quality of life during postoperatively 24 hour WHOQOL-BREF-THAI,side effect of opioid (Nausea and vomiting episode, ambulation, sedation score, RS depression) 24 hour grading score

Countries

Thailand

Contacts

Public ContactThipphawan chanasuek

Faculty of Medicine, Khon Kaen University

Thipphawan.ch@kkumail.com0635536945

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 9, 2026